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EX-23.2 - CONSENTS OF EXPERTS AND COUNSEL - VIVOS INC | ex23-2.htm |
EX-23.1 - CONSENTS OF EXPERTS AND COUNSEL - VIVOS INC | ex23-1.htm |
As filed with the Securities and Exchange Commission on March 9,
2017
Registration
No. 333-
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM S-1
REGISTRATION STATEMENT UNDER THE SECURITIES ACT OF
1933
ADVANCED MEDICAL ISOTOPE CORPORATION
(Exact
name of registrant as specified in its charter)
Delaware
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2810
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80-0138937
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(State
or other jurisdiction of incorporation or
organization)
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(Primary
Standard Industrial Classification Code Number)
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(I.R.S.
Employer Identification Number)
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1021 N Kellogg Street
Kennewick, WA 99336
(509) 736-4000
(Address,
including zip code, and telephone number,
including
area code, of registrant’s principal executive
offices)
Dr. Michael Korenko, Chief Executive Officer
Advanced Medical Isotope Corporation
1021 N Kellogg Street
Kennewick, WA 99336
(509) 736-4000
(Name,
address, including zip code, and telephone number,
including
area code, of agent for service)
Approximate
date of commencement of proposed sale to the public: As
soon as practicable after the registration statement becomes
effective.
If any
of the securities being registered on this Form are to be offered
on a delayed or continuous basis pursuant to Rule 415 under the
Securities Act of 1933 check the following box: ☒
If this
Form is filed to register additional securities for an offering
pursuant to Rule 462(b) under the Securities Act, please check the
following box and list the Securities Act registration statement
number of the earlier effective registration statement for the same
offering. ☐
If this
Form is a post-effective amendment filed pursuant to Rule 462(c)
under the Securities Act, check the following box and list the
Securities Act registration statement number of the earlier
effective registration statement for the same
offering. ☐
If this
Form is a post-effective amendment filed pursuant to Rule 462(d)
under the Securities Act, check the following box and list the
Securities Act registration statement number of the earlier
effective registration statement for the same offering.
☐
Indicate
by check mark whether the registrant is a large accelerated filer,
an accelerated filer, a non-accelerated filer, or a smaller
reporting company. See the definitions of "large
accelerated filer," "accelerated filer" and "smaller reporting
company" in Rule 12b-2 of the Exchange Act.
Large
accelerated filer
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☐
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Accelerated
filer
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☐
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Non-accelerated
filer
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☐
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Smaller
reporting company
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☒
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(Do not
check if a smaller reporting company)
CALCULATION OF REGISTRATION FEE
Title
Of Each Class Of Securities To Be Registered
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Proposed
Maximum Aggregate Offering Price (1)
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Amount
Of
Registration
Fee
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Common stock,
$0.001 par value
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$—
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$—
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Warrants to
purchase shares of common stock (2)
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$—
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$—
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Shares of common
stock issuable upon exercise of warrants (3)
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$—
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$—
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Total
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$10,000,000
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$1,159.00
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(1)
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Estimated
solely for the purpose of computing the amount of the registration
fee pursuant to Rule 457(o) under the Securities Act of 1933,
as amended (Securities
Act).
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(2)
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Represents
warrants to purchase a number of shares of common stock equal to
50% of the common stock sold in this offering at an exercise price
of 125% of the public offering price of the shares of common
stock.
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(3)
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Pursuant
to Rule 416, there is also being registered such indeterminable
additional securities as may be issued to prevent dilution as a
result of stock splits, stock dividends or similar
transactions.
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The Registrant hereby amends this Registration Statement on such
date or dates as may be necessary to delay its effective date until
the Registrant shall file a further amendment which specifically
states that this Registration Statement shall thereafter become
effective in accordance with Section 8(a) of the Securities Act of
1933, as amended, or until the Registration Statement shall become
effective on such date as the Commission, acting pursuant to said
Section 8(a), may determine.
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The information in this preliminary prospectus is not complete and
may be changed. These securities may not be sold until the
registration statement filed with Securities and Exchange
Commission is effective. This prospectus is not an offer to sell
these securities and is not soliciting an offer to buy these
securities in any state or other jurisdiction where the offer or
sale is not permitted.
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Subject to completion, dated February ____, 2017
PRELIMINARY PROSPECTUS
$10,000,000
Common Stock
Warrants to purchase Shares of Common Stock
Advanced Medical Isotope Corporation (the
“Company”) is offering shares of common stock
and warrants to purchase up to shares of our common stock to
purchasers in this offering (and the shares of common stock
issuable upon exercise of the warrants). Each share of
common stock will be sold at a price of $ per share, and will be
accompanied by a warrant to purchase share of common stock for $
per share ( % of the public offering price of our common stock) at
an exercise price of $ per warrant. The common stock and warrants
are immediately separable but can only be purchased together in
this offering. The warrants are exercisable immediately and expire
years from the date of issuance.
Our common stock is quoted on the OTC PINK
Marketplace under the symbol “ADMD”. The last reported
bid price of our common stock on March 7, 2017 was $0.15 per share. We do not intend to apply for listing of the
warrants on any securities exchange or other nationally recognized
trading system and we do not expect such a market to
develop. There is no market through which the warrants may
be sold and purchasers may not be able to resell the warrants
purchased under this prospectus. This may affect the pricing of the
warrants in the secondary market, the transparency and availability
of trading prices, the liquidity of such warrants.
An investment in our securities involves a high degree of
risk. We urge you to read carefully
the “Risk Factors” section beginning on page 7 where we
describe specific risks associated with an investment in Advanced
Medical Isotope Corporation and our securities before you make your
investment decision. You should purchase our securities only if you
can afford a complete loss of your purchase.
-i-
Neither the Securities and Exchange Commission nor any state
securities commission has approved or disapproved these securities,
or determined if this prospectus is truthful or
complete. Any representation to the contrary is a
criminal offense.
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Per
share and related warrant
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Total
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Public offering
price
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$
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$
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Offering proceeds,
before expenses, to us
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$
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$
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(1) We
estimate the total expenses of this offering payable by us will be
approximately $ .
We
anticipate that delivery of the shares and warrants against payment
will be made on or about ,
2017.
The date of this prospectus is ,
2017.
-ii-
TABLE OF CONTENTS
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PAGE
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Prospectus
Summary
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2
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Risk
Factors
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7
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Special
Note Regarding Forward-Looking Information
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16
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Use of
Proceeds
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17
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Price
Range for Common Equity and Related Stockholders
Matters
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18
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Dividends
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19
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Capitalization
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20
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Dilution
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21
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Management’s
Discussion and Analysis of Financial Condition and Results of
Operations
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22
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Description
of Business
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29
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Management
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37
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Executive
Compensation
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39
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Security
Ownership of Certain Beneficial Owners and Certain Corporate
Governance Matters
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41
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Certain
Relationships and Related Party Transactions
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43
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Description
of Securities
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44
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Shares
Eligible for Future Sale
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48
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Plan
of Distribution
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49
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Changes
In and Disagreements with Accountant on Accounting Issues and
Financial Disclosure
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50
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Legal
Matters
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50
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Experts
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50
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Where
You Can Find More Information
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51
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Index
to Financial Statements
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52
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We
have not authorized anyone to provide any information or to make
any representations other than those contained in this prospectus
or in any prospectus supplement or free writing prospectuses
prepared by or on behalf of us or to which we have referred you. We
take no responsibility for, and can provide no assurance as to the
reliability of, any other information that others may give you.
This prospectus is an offer to sell only the shares offered hereby,
and only under circumstances and in jurisdictions where it is
lawful to do so. The information contained in this prospectus or in
any applicable prospectus supplement or free writing prospectus is
current only as of its date, regardless of its time of delivery or
any sale of our securities. Our business, financial condition,
results of operations and prospects may have changed since that
date.
For investors outside the
United States: We have not done
anything that would permit this offering or possession or
distribution of this prospectus in any jurisdiction where action
for that purpose is required, other than in the United States.
Persons outside the United States who come into possession of this
prospectus must inform themselves about, and observe any
restrictions relating to, the offering of the securities and the
distribution of this prospectus outside the United
States.
-iii-
ABOUT THIS PROSPECTUS
You
should rely only on the information contained in or incorporated by
reference into this prospectus and any prospectus supplement or
free writing prospectus authorized by us. To the extent the
information contained in this prospectus differs or varies from the
information contained in any document filed prior to the date of
this prospectus and incorporated by reference, the information in
this prospectus will control. We have not authorized any other
person to provide you with different information. If anyone
provides you with different or inconsistent information, you should
not rely on it. The information in this prospectus is accurate only
as of the date it is presented. You should read this prospectus,
and any prospectus supplement or free writing prospectus that we
have authorized for use in connection with this offering, in their
entirety before investing in our securities.
We
are offering to sell, and seeking offers to buy, the securities
offered by this prospectus only in jurisdictions where offers and
sales are permitted. The distribution of this prospectus and the
offering of the securities offered by this prospectus in certain
jurisdictions may be restricted by law. This prospectus does not
constitute, and may not be used in connection with, an offer to
sell, or a solicitation of an offer to buy, any securities offered
by this prospectus in any jurisdiction in which it is unlawful for
such person to make such an offer or solicitation.
Unless the
context otherwise requires, the words “Advanced
Medical Isotope Corporation,”
“Advanced
Medical,”
“AMI,”
“we,”
“the
Company,”
“us”
and “our”
refer to Advanced Medical Isotope Corporation, a Delaware
corporation.
-1-
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PROSPECTUS SUMMARY
The following summary highlights information contained elsewhere in
this prospectus and does not contain all of the information that
you should consider in making your investment decision in our
securities. Before investing in our securities, you should
carefully read this entire prospectus, including our financial
statements and the related notes included in this prospectus and
the information set forth under the headings “Risk
Factors” and “Management’s Discussion and
Analysis of Financial Condition and Results of
Operations.”
Business Summary
Advanced Medical Isotope Corporation (the
“Company,” “AMI” or “we”) was incorporated under the laws of
Delaware on December 23, 1994 as Savage Mountain Sports
Corporation. On September 6, 2006, the Company changed its name to
Advanced Medical Isotope Corporation.
The
Company is a late stage radiation oncology medical device company
engaged in the development of its yttrium-90 based brachytherapy
device RadiogGelTM for the treatment
of non-resectable tumors. A prominent team of radiochemists,
scientists and engineers, collaborating with strategic partners,
including national laboratories, universities and private
corporations, lead the Company’s development efforts. The
Company’s overall vision is to globally empower physicians,
medical researchers and patients by providing them with new isotope
technologies that offer safe and effective treatments for
cancer.
The Company’s current focus is on the
development of its RadioGelTM device.
RadioGelTM
is an injectable particle-gel, for brachytherapy radiation
treatment of cancerous tumors in people and animals.
RadioGelTM
is comprised of a hydrogel, or a substance that is liquid at room
temperature and then gels when reaching body temperature after
injection into a tumor. In the gel are small, one micron,
yttrium-90 phosphate particles (“Y-90”). Once injected, these inert particles are
locked in place inside the tumor by the gel, delivering a very high
local radiation dose. The radiation is beta, consisting of
high-speed electrons. These electrons only travel a short distance
so the device can deliver high radiation to the tumor with minimal
dose to the surrounding tissue. Optimally, patients can go home
immediately following treatment without the risk of radiation
exposure to family members. Since Y-90 has a half-life of 2.7 days,
the radioactively drops to 5% of its original value after ten
days.
The Company’s lead brachytherapy products,
including RadioGelTM, incorporate
patented technology developed for Battelle Memorial Institute
(“Battelle”) at Pacific Northwest National Laboratory,
a leading research institute for government and commercial
customers. Battelle has granted the Company an exclusive license to
patents covering the manufacturing, processing and applications of
RadioGelTM
(the “Battelle
License”). Other
intellectual property protection includes proprietary production
processes and trademark protection in 17 countries. The Company
plans to continue efforts to develop new refinements on the
production process, and the product and application hardware, as a
basis for future patents.
The Company is currently focusing on obtaining
approval from the Food and Drug Administration
(“FDA”) to market and sell RadioGelTM as a Class II
medical device. The Company first requested FDA approval of
RadioGelTM
in June 2013, at which time the FDA classified RadioGelTM as a medical
device. The Company is currently developing test plans to address
issues raised by the FDA in connection with the Company’s
previous submissions regarding RadioGelTM.The Company intends
to request FDA approval to apply for de novo classification of RadioGelTM, which would
reclassify the device from a Class III device to a Class II device,
further simplifying the regulatory path.
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-2-
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In previous FDA submittals, the Company proposed
applying RadioGelTM for a
very broad range of cancer therapies, referred to as Indication for
Use. The FDA has requested that the Company reduce its Indications
for Use. To comply with that request, the Company has expanded its
Medical Advisory Board (“MAB”) and engaged doctors from respected
hospitals who have evaluated the candidate cancer therapies based
on three criteria: (1) potential for FDA approval and successful
therapy; (2) notable advantage over current therapies; and (3)
probability of wide spread acceptance by the medical
community.
The
MAB selected eighteen applications for RadioGelTM,
each of which meet the criteria described above. This large number
confirms the wide applicability of the device and defines the path
for future business growth. The Company intends to apply to the FDA
for a single Indication for Use, followed by subsequent
applications for additional Indications for Use. The initial
application should facilitate each subsequent application, and the
testing for many of the subsequent applications could be conducted
in parallel, depending on available resources.
The
MAB selected the treatment of basal cell and squamous cell skin
cancers for the first Indication for Use to be submitted to the
FDA. According to the American Cancer Society, one out of every
three new cancers diagnosed in the U.S. is a cancerous skin lesion
of this type, representing 5.5 million tumors diagnosed annually.
The MAB believes RadioGelTM
has the potential to be the preferred treatment in a reasonable
number of cases in a very large market.
The
Company’s, IsoPet Solutions division was established in May
2016 to focus on the veterinary oncology market. The Company has
engaged four different university veterinarian hospitals to begin
using RadioGelTM
for treatment of four different cancer types in dogs and cats.
Washington State University Veterinary Hospital has tested one cat
to demonstrate the procedures and the absence of any significant
toxicity effect. The other three centers are expected to begin
therapy during the second quarter of 2017 after their internal
administrative review process is completed.
These
animal therapies will focus on creating labels that describe the
procedures in detail as a guide to future veterinarians. The labels
will be voluntarily submitted to the FDA for review. They will then
be used as data for future FDA applications in the medical sector
and as key intellectual property for licensing to private
veterinary clinics. In 2018, Dr. Alice Villalobos, the Chair of our
Veterinarian Advisory Board, will be the first licensee of these
therapies in her private clinic to demonstrate the business
model.
The
Company anticipates that future profit will be derived from direct
sales of RadioGelTMand
related services, and from licensing to private medical and
veterinary clinics in the U.S. and internationally.
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-3-
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The
Offering
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Common stock we are offering
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shares of common stock
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Warrants we are offering
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Each share of common stock sold in this offering will be
accompanied by a warrant to purchase share of our common stock, at
an exercise price of $ per share
( % of the public
offering price of our common stock). The warrants will be
immediately exercisable, and may be exercised for a period
of
years
following the date of issuance. This prospectus also covers the
shares of common stock issuable upon exercise of the warrants
offered hereby.
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Common stock outstanding after this offering
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shares of common
stock
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Use of proceeds
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We
estimate that the net proceeds to us from this offering, after
deducting the estimated offering expenses payable by us, will be
approximately $ million, excluding any proceeds we may
receive upon exercise of the warrants, if any. We intend to use the
net proceeds of this offering for working capital and general
corporate purposes, including sales and marketing activities,
product development, capital expenditures, the potential repayment
of certain debt of the Company and product acquisitions and product
licenses. See “Use of
Proceeds” for a more complete description of the
intended use of proceeds from this offering.
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Dividend policy
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We have
never declared or paid and do not anticipate declaring or paying
any cash dividends on our common stock in the near future. You
should read the “Dividend
Policy” section of this prospectus for more
information on future declarations and payments of
dividends.
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Risk factors
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You
should read the “Risk
Factors” section of this prospectus and the other
information in this prospectus for a discussion of factors to
consider carefully before deciding to invest in shares of our
common stock.
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OTC pink marketplace symbol
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“ADMD.”
We do not intend to apply for listing of the warrants on any
securities exchange or other nationally recognized trading system
and we do not expect such a market to develop.
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-4-
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The
number of shares of our common stock to be outstanding after this
offering is based on 31,743,797 shares of our common stock
outstanding as of December 31, 2016 and excludes the following, in
each case as of such date:
●
1,932,062 shares of common stock issuable upon the exercise of
stock options outstanding as of December 31, 2016, at a weighted
average exercise price of $0.81 per share;
● 3,579,505
shares of common stock issuable upon the exercise of warrants
outstanding as of December 31, 2016, at a weighted average exercise
price of $4.45 per share;
● 4,989,395
shares of common stock issuable upon the conversion of Series A
Convertible Preferred Stock (“Series A Preferred”);
and
●
shares of common stock issuable upon exercise of warrants to be
issued in connection with this offering.
Except
as otherwise indicated, all information in this prospectus assumes
no exercise of the outstanding options and warrants or the
conversion of restricted stock units into common shares described
above.
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-5-
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SUMMARY CONSOLIDATED FINANCIAL DATA
The
summary consolidated statements of operations data presented below
for the years ended December 31, 2016 and 2015 are derived
from our audited financial statements included elsewhere in this
prospectus. The following summary consolidated financial data
should be read with “Management’s Discussion and Analysis of
Financial Condition and Results of Operations” and our
financial statements and related notes included elsewhere in this
prospectus. Our historical results are not necessarily indicative
of the results that may be expected in any future period. The
summary financial data in this section are not intended to replace
the financial statements and are qualified in their entirety by the
financial statements and related notes included elsewhere in this
prospectus.
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Year
ended
December
31,
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2016
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2015
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Consulting
Revenues
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$8,108
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$24,108
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Operating
expenses
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Cost of
materials
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-
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474
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Sales and marketing
expenses
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284,138
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-
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Depreciation and
amortization expense
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2,947
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5,672
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Professional
fees
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2,068,796
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741,375
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Stock based
compensation
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675,324
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80,635
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Payroll
expenses
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652,877
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679,259
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Research and
development
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328,026
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149,650
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General and
administrative expenses
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432,470
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408,306
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Total operating
expenses
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4,444,578
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2,065,371
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Operating
loss
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(4,436,470)
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(2,041,263)
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Non-operating
income (expense):
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Interest
expense
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(6,259,467)
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(3,196,153)
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Gain on settlement
of debt
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3,108,342
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3,562,067
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Gain (loss) on
derivative liability
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(2,244,353)
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7,887,025
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Grant
income
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21,010
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21,010
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Loss on impaired
assets
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(43,957)
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Non-operating
income (expense), net
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(5,418,425)
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8,273,949
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Income (loss)
before Income Taxes
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(9,854,895)
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6,232,686
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Income tax
provision
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Net income
(loss)
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$(9,854,895)
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$6,232,686
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Earnings (loss) per
common share
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$(0.46)
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$0.34
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Weighted average
number of common shares outstanding
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21,497,069
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18,505,467
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(1)
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See
Note 2 to our audited consolidated financial statements for an
explanation of the method used to calculate basic and diluted net
loss per common share and the weighted-average number of shares
used in the computation of the per share amounts.
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Consolidated
Balance Sheet Data:
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At December 31, 2016
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Actual
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As Adjusted (1)(2)
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Cash and cash
equivalents
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$27,889
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Total
assets
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41,996
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Accounts payable
and accrued expenses
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1,137,086
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Related party accounts payable
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109,718
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Accrued interest
payable
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114,755
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Payroll liabilities
payable
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499,502
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Convertible notes
payable, net
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544,508
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Derivative
liability
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324,532
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Related party
promissory note
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332,195
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Total
stockholders’ equity (deficit)
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(17,164,871)
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(1)
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The as
adjusted balance sheet data gives effect to the sale
of
shares of common stock by us in this offering based on an offering
price of $ per share after deducting estimated offering expenses
payable by us.
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(2)
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Each
$0.10 increase (decrease) in the offering price of $ per
share would increase (decrease) each of our as adjusted cash and
cash equivalents, total assets and total stockholders’ equity
(deficit) by approximately $ , assuming that the number of
shares offered by us, remains the same and after deducting
estimated commissions. Similarly, each increase (decrease)
of shares in the
number of shares offered by us would increase (decrease) each of
our as adjusted cash and cash equivalents, total assets and total
stockholders’ equity (deficit) by approximately $ ,
assuming the offering price remains the same and after deducting
estimated expenses.
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-6-
RISK FACTORS
Investing in our common stock involves a high degree of risk. You
should carefully consider the risks described below, as well as the
other information in this prospectus, including our consolidated
financial statements and the related notes and
“Management’s Discussion and Analysis of Financial
Condition and Results of Operations,” before deciding whether
to invest in our securities. The occurrence of any of the events or
developments described below could harm our business, financial
condition, operating results, and growth prospects. In such an
event, the market price of our common stock could decline, and you
may lose all or part of your investment. Additional risks and
uncertainties not presently known to us or that we currently deem
immaterial also may impair our business
operations.
RISKS ASSOCIATED WITH THE COMPANY’S BUSINESS
Our independent registered public accounting firms’ reports
on its financial statements questions the Company’s ability
to continue as a going concern.
The
Company’s independent registered public accounting
firms’ reports on the Company’s financial statements
for the years ended December 31, 2016 and 2015 express doubt about
the Company’s ability to continue as a going
concern. The reports include an explanatory paragraph
stating that the Company has suffered recurring losses, used
significant cash in support of its operating activities and, based
on its current operating levels, require additional capital or
significant restructuring to sustain its operation for the
foreseeable future. There is no assurance that the Company will be
able to obtain sufficient additional capital to continue its
operations and to alleviate doubt about its ability to continue as
a going concern. If the Company obtains additional financing, such
funds may not be available on favorable terms and likely would
entail considerable dilution to existing shareholders. Any debt
financing, if available, may involve restrictive covenants that
restrict its ability to conduct its business. It is
extremely remote that the Company could obtain any financing on any
basis that did not result in considerable dilution for
shareholders. Inclusion of a “going concern
qualification” in the report of its independent accountants
or in any future report may have a negative impact on its ability
to obtain debt or equity financing and may adversely impact its
stock price.
A combination of our current financial condition and the
FDA’s determinations to date regarding our brachytherapy
products raise material concerns about ability to continue as a
going concern.
The
Company will not be able to continue as a going concern unless the
Company obtains financing. Depending upon the amount of financing,
if any, the Company is able to obtain, the Company may not receive
adequate funds to continue the approval process for
RadioGelTM
or other brachytherapy products with the FDA.
The Company has
generated operating losses since inception, which are expected to
continue, and has increasing cash requirements, which it may be
unable to satisfy.
The
Company has generated material operating losses since
inception. The Company has had recurring net losses
since inception which has resulted in an accumulated deficit of
$57,869,440 as of December 31, 2016, including a net loss of
$9,854,895 for the year ended December 31, 2016 and a net income of
$6,232,686 for the year ended December 31,
2015. Historically, the Company has relied upon investor
funds to maintain its operations and develop its
business. The Company needs to raise additional capital
within the next quarter from investors for working capital as well
as business expansion, and there is no assurance that additional
investor funds will be available on terms acceptable to the
Company, or at all. If the Company is unable to unable
to obtain additional financing to meet its working capital
requirements, the Company likely would cease
operations.
The
Company requires funding of at least $1.5 million per year to
maintain current operating activities. Over the next 12 to 24
months, the Company believes it will cost approximately $5.0
million to $10.0 million to fund: (1) the FDA approval process and
initial deployment of the brachytherapy products, and (2) initiate
regulatory approval processes outside of the United States. The
continued deployment of the brachytherapy products and a worldwide
regulatory approval effort will require additional resources and
personnel. The principal variables in the timing and
amount of spending for the brachytherapy products in the next 12 to
24 months will be the FDA’s classification of the
Company’s brachytherapy products as Class II or Class III
devices (or otherwise) and any requirements for additional studies,
which may possibly include clinical studies. Thereafter,
the principal variables in the amount of the Company’s
spending and its financing requirements would be the timing of any
approvals and the nature of the Company’s arrangements with
third parties for manufacturing, sales, distribution and licensing
of those products and the products’ success in the U.S. and
elsewhere. The Company intends to fund its activities through
strategic transactions such as licensing and partnership agreements
or additional capital raises.
-7-
Recent
economic events, including the inherent instability in global
capital markets, as well as the lack of liquidity in the capital
markets, could adversely impact the Company’s ability to
obtain financing and its ability to execute its business
plan.
The Company has a limited operating history, which may make it
difficult to evaluate its business and prospects.
The
Company has a limited operating history upon which one can base an
evaluation of its business and prospects. As a company
in the development stage, there are substantial risks,
uncertainties, expenses and difficulties to which its business is
subject. To address these risks and uncertainties, the
Company must do the following:
●
successfully
develop and execute the business strategy;
●
respond to
competitive developments; and
●
attract,
integrate, retain and motivate qualified personnel.
There
is no assurance that the Company will achieve or maintain
profitable operations or that the Company will obtain or maintain
adequate working capital to meet its obligations as they become
due. The Company cannot be certain that its business
strategy will be successfully developed and implemented or that the
Company will successfully address the risks that face its
business. In the event that the Company does not
successfully address these risks, its business, prospects,
financial condition, and results of operations could be materially
and adversely affected.
The Company’s new products are regulated and require
appropriate clearances and approvals to be marketed in the U.S. and
globally.
There
is no assurance the FDA or other global regulatory authorities will
grant the Company permission to market the Company’s
products, including the Company’s brachytherapy Y-90
RadioGelTM
device, Y-90 Fast-Resorbable Polymer Seeds and Y-90 Polymer Topical
Paste.
The Company has been working with the FDA to
obtain clearance for its brachytherapy Y-90
RadioGelTM
device, but no assurances have been received. On
December 23, 2014, the Company announced that it submitted
a de
novo to the FDA for
marketing clearance for its patented Y-90
RadioGelTM
device pursuant to Section 513(f)(2) of the U.S. Food, Drug and
Cosmetic Act (the “Act”). In June 2015 the FDA notified the
Company the de novo was not granted. In February 2014, the FDA
found the same device under Section 510(k) of the Act not
substantially equivalent, and concluded that the device is
classified by statute as a Class III medical device, unless the
device is reclassified. By filing the de novo, the Company is seeking reclassification of the
product to Class II. If the de novo is granted, as a regulatory matter, the
device could be immediately marketed in the United States, though,
as a practical matter, the Company would have to secure funding and
commercial arrangements before marketing could commence. If
the de
novo is declined and if
the Company obtains funding to permit it to continue operations,
the Company will explore steps toward seeking approval for the
device as a Class III medical device. Generally, the time period
and cost of seeking approval as a Class III medical device is
materially greater than the time period and cost of seeking
approval as a Class II medical device. If the Company
seeks approval as a Class III device, human clinical trials will be
necessary. Generally, human trials for Class III
products are larger, of longer duration and more costly than those
for Class II devices. If human clinical trials are
necessary, there will be additional cost and time to reach
marketing clearance or approval. Unless the Company
obtains sufficient funding it will be unable to do the foregoing
activities. There can be no assurance that the product
will be approved as either a Class II or Class III device by the
FDA even if additional data is provided. There can be no assurance
that the Company will receive FDA approval, or the timing
thereof.
-8-
If the Company is successful in increasing the size of its
organization, the Company may experience difficulties in managing
growth.
The
Company is a small organization with a minimal number of
employees. If the Company is successful, it may
experience a period of significant expansion in headcount,
facilities, infrastructure and overhead and further expansion may
be required to address potential growth and market
opportunities. Any such future growth will impose
significant added responsibilities on members of management,
including the need to improve the Company’s operational and
financial systems and to identify, recruit, maintain and integrate
additional managers. The Company’s future
financial performance and its ability to compete effectively will
depend, in part, on the ability to manage any future growth
effectively.
The Company’s business is dependent upon the continued
services of the Company’s Chief Executive Officer, Michael
Korenko. Should the Company lose the services of Mr. Korenko,
the Company’s operations will be negatively
impacted.
The
Company’s business is dependent upon the expertise of its
Chief Executive Officer, Michael Korenko. Mr. Korenko is essential
to the Company’s operations. Accordingly, an investor must
rely on Mr. Korenko’s management decisions that will continue
to control the Company’s business affairs. The Company does
not maintain key man insurance on Mr. Korenko’s life. The
loss of the services of Mr. Korenko would have a material adverse
effect upon the Company’s business.
The Company is heavily dependent on consultants for many of the
services necessary to continue operations. The loss of
any of these consultants could have a material adverse effect on
the Company’s business, results of operations and financial
condition.
The
Company’s success is heavily dependent on the continued
active participation of certain consultants and collaborating
scientists. Certain key employees and consultants have
no written employment contracts. Loss of the services of any one or
more of its consultants could have a material adverse effect upon
the Company’s business, results of operations and financial
condition.
If the Company is unable to hire and retain additional qualified
personnel, the business and financial condition may
suffer.
The
Company’s success and achievement of its growth plans depend
on its ability to recruit, hire, train and retain highly qualified
technical, scientific, regulatory and managerial employees,
consultants and advisors. Competition for qualified
personnel among pharmaceutical and biotechnology companies is
intense, and an inability to attract and motivate additional highly
skilled personnel required for the expansion of the Company’s
activities, or the loss of any such persons, could have a material
adverse effect on its business, results of operations and financial
condition.
The Company’s revenues have historically been derived from
sales made to a small number of customers. The Company
has discontinued prior operations related to its core business. To
succeed, we will need to recommence our operations and achieve
sales to a materially larger number of customers.
During
2014, the Company ceased all previous manufacturing an5d sales
activities. Our sales for the year ended December 31, 2016 and 2015
consisted of only consulting revenue. The Company’s
consulting revenues for the years ended December 31, 2016 and 2015
were made to one customer, and those sales constituted 100.0% of
total revenues for those years. At such time as the Company
recommences active operations, no assurances can be given that the
Company will be successful in commercializing its products or
expanding the number of customers purchasing its products and
services.
Many of the
Company’s competitors have greater resources and experience
than the Company has.
Many
of the Company’s competitors have greater financial
resources, longer history, broader experience, greater name
recognition, and more substantial operations than the Company has,
and they represent substantial long-term competition for
us. The Company’s competitors may be able to
devote more financial and human resources than the Company can to
research, new product development, regulatory approvals, and
marketing and sales. The Company’s competitors may
develop or market products that are viewed by customers as more
effective or more economical than the Company’s
products. There is no assurance that the Company will be
able to compete effectively against current and future competitors,
and such competitive pressures may adversely affect the
Company’s business and results of operations.
-9-
The Company’s future revenues depend upon acceptance of its
current and future products in the markets in which they
compete.
The
Company’s future revenues depend upon receipt of financing,
regulatory approval and the successful production, marketing, and
sales of the various isotopes the Company might market in the
future. The rate and level of market acceptance of each
of these products, if any, may vary depending on the perception by
physicians and other members of the healthcare community of its
safety and efficacy as compared to that of any competing products;
the clinical outcomes of any patients treated; the effectiveness of
its sales and marketing efforts in the United States, Europe, Far
East, Middle East, and Russia; any unfavorable publicity concerning
its products or similar products; the price of the Company’s
products relative to other products or competing treatments; any
decrease in current reimbursement rates from the Centers for
Medicare and Medicaid Services or third-party payers; regulatory
developments related to the manufacture or continued use of its
products; availability of sufficient supplies to either purchase or
manufacture its products; its ability to produce sufficient
quantities of its products; and the ability of physicians to
properly utilize its products and avoid excessive levels of
radiation to patients. Any material adverse developments
with respect to the commercialization of any such products may
adversely affect revenues and may cause the Company to continue to
incur losses in the future.
The Company will in the future rely heavily on a limited number of
suppliers.
Some
of the products the Company might market and components thereof are
currently available only from a limited number of suppliers,
several of which are international suppliers. Failure to
obtain deliveries from these sources could have a material adverse
effect on the Company’s ability to operate.
The Company may incur material losses and costs as a result of
product liability claims that may be brought against
it.
The
Company faces an inherent business risk of exposure to product
liability claims in the event that products supplied by the Company
fail to perform as expected or such products result, or is alleged
to result, in bodily injury. Any such claims may also
result in adverse publicity, which could damage the Company’s
reputation by raising questions about the safety and efficacy of
its products, and could interfere with its efforts to market its
products. A successful product liability claim against
the Company in excess of its available insurance coverage or
established reserves may have a material adverse effect on its
business. Although the Company currently maintains
liability insurance in amounts it believes are commercially
reasonable, any product liability the Company may incur may exceed
its insurance coverage.
The Company is subject to the risk that certain third parties may
mishandle the Company’s products.
If
the Company markets products, the Company likely will rely on third
parties, such as commercial air courier companies, to deliver the
products, and on other third parties to package the products in
certain specialized packaging forms requested by
customers. The Company thus would be subject to the risk
that these third parties may mishandle its product, which could
result in material adverse effects, particularly given the
radioactive nature of some of the products.
The Company’s operations expose it to the risk of material
environmental liabilities.
The
Company is subject to potentially material liabilities related to
the remediation of environmental hazards and to personal injuries
or property damages that may be caused by hazardous substance
releases and exposures. The Company is subject to
various federal, state, local and foreign government requirements
regulating the discharge of materials into the environment or
otherwise relating to the protection of the
environment. These laws and regulations can impose
substantial fines and criminal sanctions for violations, and can
require installation of costly equipment or operational changes to
limit emissions and/or decrease the likelihood of accidental
hazardous substance releases. The Company expects to
incur capital and operating costs to comply with these laws and
regulations. In addition, changes in laws, regulations
and enforcement of policies, the discovery of previously unknown
contamination or new technology or information related to
individual sites, or the imposition of new clean-up requirements or
remedial techniques may require the Company to incur costs in the
future that would have a negative effect on its financial condition
or results of operations. Operational hazards could
result in the spread of contamination within the Company’s
facility and require additional funding to correct.
-10-
The Company is subject to uncertainties regarding reimbursement for
use of its products.
Hospitals
and freestanding clinics may be less likely to purchase the
Company’s products if they cannot be assured of receiving
favorable reimbursement for treatments using its products from
third-party payers, such as Medicare and private health insurance
plans. Third-party payers are increasingly challenging
the pricing of certain medical services or devices, and there is no
assurance that they will reimburse the Company’s customers at
levels sufficient for it to maintain favorable sales and price
levels for the Company’s products. There is no
uniform policy on reimbursement among third-party payers, and there
is no assurance that the Company’s products will continue to
qualify for reimbursement from all third-party payers or that
reimbursement rates will not be reduced. A reduction in
or elimination of third-party reimbursement for treatments using
the Company’s products would likely have a material adverse
effect on the Company’s revenues.
The Company’s future growth is largely dependent upon its
ability to develop new technologies that achieve market acceptance
with appropriate margins.
The
Company’s business operates in global markets that are
characterized by rapidly changing technologies and evolving
industry standards. Accordingly, future growth rates
depends upon a number of factors, including the Company’s
ability to (i) identify emerging technological trends in the
Company’s target end-markets, (ii) develop and maintain
competitive products, (iii) enhance the Company’s products by
adding innovative features that differentiate the Company’s
products from those of its competitors, and (iv) develop,
manufacture and bring products to market quickly and
cost-effectively. The Company’s ability to develop
new products based on technological innovation can affect the
Company’s competitive position and requires the investment of
significant resources. These development efforts divert
resources from other potential investments in the Company’s
business, and they may not lead to the development of new
technologies or products on a timely basis or that meet the needs
of the Company’s customers as fully as competitive
offerings. In addition, the markets for the
Company’s products may not develop or grow as it currently
anticipates. The failure of the Company’s
technologies or products to gain market acceptance due to more
attractive offerings by the Company’s competitors could
significantly reduce the Company’s revenues and adversely
affect the Company’s competitive standing and
prospects.
The Company may rely on third parties to represent it locally in
the marketing and sales of its products in international markets
and its revenue may depend on the efforts and results of those
third parties.
The
Company’s future success may depend, in part, on its ability
to enter into and maintain collaborative relationships with one or
more third parties, the collaborator’s strategic interest in
the Company’s products and the Company’s products under
development, and the collaborator’s ability to successfully
market and sell any such products. The Company intends
to pursue collaborative arrangements regarding the marketing and
sales of its products; however, it may not be able to establish or
maintain such collaborative arrangements, or if it is able to do
so, the Company’s collaborators may not be effective in
marketing and selling its products. To the extent that
the Company decides not to, or is unable to, enter into
collaborative arrangements with respect to the sales and marketing
of its products, significant capital expenditures, management
resources and time will be required to establish and develop an
in-house marketing and sales force with technical
expertise. To the extent that the Company depends on
third parties for marketing and distribution, any revenues received
by the Company will depend upon the efforts and results of such
third parties, which may or may not be successful.
The Company may pursue strategic acquisitions that may have an
adverse impact on its business.
Executing
the Company’s business strategy may involve pursuing and
consummating strategic transactions to acquire complementary
businesses or technologies. In pursuing these strategic
transactions, even if the Company does not consummate them, or in
consummating such transactions and integrating the acquired
business or technology, the Company may expend significant
financial and management resources and incur other significant
costs and expenses. There is no assurance that any
strategic transactions will result in additional revenues or other
strategic benefits for the Company’s business. The
Company may issue the Company’s stock as consideration for
acquisitions, joint ventures or other strategic transactions, and
the use of stock as purchase consideration could dilute the
interests of its current stockholders. In addition, the
Company may obtain debt financing in connection with an
acquisition. Any such debt financing may involve
restrictive covenants relating to capital-raising activities and
other financial and operational matters, which may make it more
difficult for the Company to obtain additional capital and pursue
business opportunities, including potential
acquisitions. In addition, such debt financing may
impair the Company’s ability to obtain future additional
financing for working capital, capital expenditures, acquisitions,
general corporate or other purposes, and a substantial portion of
cash flows, if any, from the Company’s operations may be
dedicated to interest payments and debt repayment, thereby reducing
the funds available to the Company for other purposes.
-11-
The Company will need to hire additional qualified accounting
personnel in order to remediate a material weakness in its internal
control over financial accounting, and the Company will need to
expend any additional resources and efforts that may be necessary
to establish and to maintain the effectiveness of its internal
control over financial reporting and its disclosure controls and
procedures.
As
a public company, the Company is subject to the reporting
requirements of the Securities Exchange Act of 1934, as amended,
and the Sarbanes-Oxley Act of 2002. The Company’s
management is required to evaluate and disclose its assessment of
the effectiveness of the Company’s internal control over
financial reporting as of each year-end, including disclosing any
“material weakness” in the Company’s internal
control over financial reporting. A material weakness is
a control deficiency, or combination of control deficiencies, that
results in more than a remote likelihood that a material
misstatement of the annual or interim financial statements will not
be prevented or detected. As a result of its assessment,
management has determined that there is a material weakness due to
the lack of segregation of duties and, due to this material
weakness, management concluded that, as of December 31, 2016 and
2015, the Company’s internal control over financial reporting
was ineffective. This material weakness was first identified in the
Company’s Form 10-K/A amended annual report for the year
ended December 31, 2008. This material weakness has the potential
of adversely impacting the Company’s financial reporting
process and the Company’s financial
reports. Because of this material weakness, management
also concluded that the Company’s disclosure controls and
procedures were ineffective as of December 31, 2016 and
2015. The Company needs to hire additional
qualified accounting personnel in order to resolve this material
weakness. The Company also will need to expend any
additional resources and efforts that may be necessary to establish
and to maintain the effectiveness of the Company’s internal
control over financial reporting and disclosure controls and
procedures.
The Company may be unable to make timely license and patent
payments
Patent
costs associated with existing and new technology are
significant. Existing patent and license fees must be
paid for the Company to maintain rights to the
technology. The Company would forfeit its exclusive
rights to licensed technologies without paying patent and rights
fees in a timely fashion. There is no assurance of
sufficient capital to meet ongoing legal costs associated with the
patent costs for the Company’s technology.
The Company’s patented or other technologies may infringe on
other patents, which may expose it to costly
litigation.
It
is possible that the Company’s patented or other technologies
may infringe on patents or other rights owned by
others. The Company may have to alter its products or
processes, pay licensing fees, defend infringement actions or
challenge the validity of the patents in court, or cease activities
altogether because of patent rights of third parties, thereby
causing additional unexpected costs and delays to the
Company. Patent litigation is costly and time consuming,
and the Company may not have sufficient resources to pursue such
litigation. If the Company does not obtain a license
under such patents, if it is found liable for infringement, or if
it are not able to have such patents declared invalid, the Company
may be liable for significant money damages, may encounter
significant delays in bringing products to market or may be
precluded from participating in the manufacture, use or sale of
products or methods of treatment requiring such
licenses.
Protecting the Company’s intellectual property is critical to
its innovation efforts.
The
Company owns or has a license to use several U.S. and foreign
patents and patent applications, trademarks and
copyrights. The Company’s intellectual property
rights may be challenged, invalidated or infringed upon by third
parties, or it may be unable to maintain, renew or enter into new
licenses of third party proprietary intellectual property on
commercially reasonable terms. In some non-U.S.
countries, laws affecting intellectual property are uncertain in
their application, which can adversely affect the scope or
enforceability of the Company’s patents and other
intellectual property rights. Any of these events or
factors could diminish or cause the Company to lose the competitive
advantages associated with the Company’s intellectual
property, subject the Company to judgments, penalties and
significant litigation costs, or temporarily or permanently disrupt
its sales and marketing of the affected products or
services.
-12-
The Company may not be able to protect its trade secrets and other
unpatented proprietary technology, which could give competitors an
advantage.
The
Company relies upon trade secrets and other unpatented proprietary
technology. The Company may not be able to adequately
protect its rights with regard to such unpatented proprietary
technology, or competitors may independently develop substantially
equivalent technology. The Company seeks to protect
trade secrets and proprietary knowledge, in part through
confidentiality agreements with its employees, consultants,
advisors and collaborators. Nevertheless, these
agreements may not effectively prevent disclosure of the
Company’s confidential information and may not provide the
Company with an adequate remedy in the event of unauthorized
disclosure of such information, and as a result the
Company’s competitors could gain a competitive
advantage.
General economic conditions in markets in which the Company does
business can impact the demand for the Company’s goods and
services. Decreased demand for the Company’s products and
services could have a negative impact on its financial performance
and cash flow.
Demand
for the Company’s products and services, in part, depends on
the general economic conditions affecting the countries and
industries in which the Company does business. A
downturn in economic conditions in a country or industry that the
Company serves may adversely affect the demand for the
Company’s products and services, in turn negatively impacting
the Company’s operations and financial
results. Further, changes in demand for the
Company’s products and services can magnify the impact of
economic cycles on the Company’s
businesses. Unanticipated contract terminations by
current customers can negatively impact operations, financial
results and cash flow. The Company’s earnings,
cash flow and financial position are exposed to financial market
risks worldwide, including interest rate and currency exchange rate
fluctuations and exchange rate
controls. Fluctuations in domestic and world
financial markets could adversely affect interest rates and impact
the Company’s ability to obtain credit or attract
investors.
The Company is subject to extensive government regulation in
jurisdictions around the world in which it does business.
Regulations address, among other things, environmental compliance,
import/export restrictions, healthcare services, taxes and
financial reporting, and those regulations can significantly
increase the cost of doing business, which in turn can negatively
impact operations, financial results and cash flow.
If
the Company is successful in developing manufacturing capability,
the Company will be subject to extensive government regulation and
intervention both in the U.S. and in all foreign jurisdictions in
which it conducts business. Compliance with applicable
laws and regulations will result in higher capital expenditures and
operating costs, and changes to current regulations with which the
Company complies can necessitate further capital expenditures and
increases in operating costs to enable continued
compliance. Additionally, from time to time, the Company
may be involved in proceedings under certain of these laws and
regulations. Foreign operations are subject to political
instabilities, restrictions on funds transfers, import/export
restrictions, and currency fluctuation.
Volatility in raw material and energy costs, interruption in
ordinary sources of supply, and an inability to recover from
unanticipated increases in energy and raw material costs could
result in lost sales or could increase significantly the cost of
doing business.
Market
and economic conditions affecting the costs of raw materials,
utilities, energy costs, and infrastructure required to provide for
the delivery of the Company’s products and services are
beyond the Company’s control. Any disruption or
halt in supplies, or rapid escalations in costs, could adversely
affect the Company’s ability to manufacture products or to
competitively price the Company’s products in the
marketplace. To date, the ultimate impact of energy
costs increases have been mitigated through price increases or
offset through improved process efficiencies; however, continuing
escalation of energy costs could have a negative impact upon the
Company’s business and financial performance.
-13-
RISKS RELATED TO THE COMPANY’S COMMON STOCK
The Company’s common stock is listed on the OTC Bulletin
Board. Failure to develop or maintain a more active trading market
may negatively affect the value of the Company’s common
stock, may deter some potential investors from purchasing the
Company’s common stock or other equity securities, and may
make it difficult or impossible for stockholders to sell their
shares of common stock.
The
Company’s average daily volume of shares traded for the years
ended December 31, 2016 and 2015 was 113,034 and 403,927,
respectively. Failure to develop or maintain an active trading
market may negatively affect the value of the Company’s
common stock, may make some potential investors unwilling to
purchase the Company’s common stock or equity securities that
are convertible into or exercisable for the Company’s common
stock, and may make it difficult or impossible for the
Company’s stockholders to sell their shares of common stock
and recover any part of their investment.
The Company’s outstanding securities, the stock or securities
that it may become obligated to issue under existing agreements,
and certain provisions of those securities, may cause immediate and
substantial dilution to existing stockholders and may make it more
difficult to raise additional equity capital.
The
Company had 37,541,697 shares of common stock outstanding on March
6, 2017. The Company also had outstanding on that date
derivative securities consisting of options, warrants, and
convertible notes that if they had been exercised and converted in
full on March 6, 2017, would have resulted in the issuance of up to
11,637,245 additional shares of common stock. The
issuance of shares upon the exercise of options or the conversion
of convertible notes may result in substantial dilution to each
stockholder by reducing that stockholder’s percentage
ownership of the Company’s total outstanding common
stock. Additionally, the Company has outstanding notes
that if not prepaid by specific dates entitle the holder to convert
the principal and accrued interest into common stock at 60% of the
lowest trading price during the previous thirty day trading period
of the Company’s common stock prior to conversion as provided
in the notes. See Note 11 of the footnotes to the Consolidated
Financial Statements for the years ended December 31, 2016 and 2015
beginning on page F-1 of this
prospectus regarding the equity issuable upon
conversion. The issuance of some or all of those warrants and any
exercise of those warrants will have the effect of further diluting
the percentage ownership of the Company’s other stockholders.
That agreement also provides for stock compensation for consulting
services. The existence and terms of these derivative securities
and other obligations may make it more difficult for the Company to
raise additional capital through the sale of stock or other equity
securities.
Future sales of the Company’s stock, including sales
following exercise or conversion of derivative securities, or the
perception that such sales may occur, may depress the price of
common stock and could encourage short sales.
The
sale or availability for sale of substantial amounts of the
Company’s shares in the public market, including shares
issuable upon exercise of options or warrants or upon the
conversion of convertible securities, or the perception that such
sales may occur, may adversely affect the market price of the
Company’s common stock. Any decline in the price
of the Company’s common stock may encourage short sales,
which could place further downward pressure on the price of the
Company’s common stock.
The Company’s stock price is likely to be
volatile.
For
the year ended December 31, 2016, the reported low closing price
for the Company’s common stock was $0.07 per share, and the
reported high closing price was $0.96 per share. For the
year ended December 31, 2015, the reported low closing price for
the Company’s common stock was $0.03 per share, and the
reported high closing price was $0.49 per share. There
is generally significant volatility in the market prices, as well
as limited liquidity, of securities of early stage companies,
particularly early stage medical product
companies. Contributing to this volatility are various
events that can affect the Company’s stock price in a
positive or negative manner. These events include, but
are not limited to: governmental approvals, refusals to approve,
regulations or other actions; market acceptance and sales growth of
the Company’s products; litigation involving the Company or
the Company’s industry; developments or disputes concerning
the Company’s patents or other proprietary rights; changes in
the structure of healthcare payment systems; departure of key
personnel; future sales of its securities; fluctuations in its
financial results or those of companies that are perceived to be
similar to us; investors’ general perception of us; and
general economic, industry and market conditions. If any
of these events occur, it could cause the Company’s stock
price to fall, and any of these events may cause the
Company’s stock price to be volatile.
The Company’s common stock is subject to the “Penny
Stock” rules of the SEC and the trading market in its
securities is limited, which makes transactions in its common stock
cumbersome and may reduce the value of an investment in the
Company’s stock.
The
Securities and Exchange Commission has adopted Rule 3a51-1 which
establishes the definition of a “penny stock,” for the
purposes relevant to us, as any equity security that has a market
price of less than $5.00 per share or with an exercise price of
less than $5.00 per share, subject to certain
exceptions. For any transaction involving a penny stock,
unless exempt, Rule 15g-9 requires that a broker or dealer approve
a person’s account for transactions in penny stocks and that
the broker or dealer receive from the investor a written agreement
to the transaction, setting forth the identity and quantity of the
penny stock to be purchased.
In
order to approve a person’s account for transactions in penny
stocks, the broker or dealer must obtain financial information and
investment experience and objectives of the person and must make a
reasonable determination that the transactions in penny stocks are
suitable for that person and that the person has sufficient
knowledge and experience in financial matters to be capable of
evaluating the risks of transactions in penny stocks.
The
broker or dealer must also deliver, prior to any transaction in a
penny stock, a disclosure schedule prescribed by the SEC relating
to the penny stock market, which sets forth the basis on which the
broker or dealer made the suitability determination, and that the
broker or dealer received a signed, written agreement from the
investor prior to the transaction.
Generally, brokers may be less willing to execute
transactions in securities subject to the “penny stock”
rules. This may make it more difficult for investors to
dispose of the Company’s common stock and may cause a decline
in the market value of its stock.
Disclosure
also has to be made about the risks of investing in penny stocks in
both public offerings and in secondary trading and about the
commissions payable to both the broker-dealer and the registered
representative, current quotations for the securities and the
rights and remedies available to an investor in cases of fraud in
penny stock transactions. Finally, monthly statements
have to be sent disclosing recent price information for the penny
stock held in the account and information on the limited market in
penny stocks.
As a result of the Company issuing preferred stock, the rights of
holders of the Company’s common stock and the value of the
Company’s common stock may be adversely
affected.
The Company’s
board of directors is authorized to issue classes or series of
preferred stock, without any action on the part of the
stockholders. The Company’s board of directors
also has the power, without stockholder approval, to set the terms
of any such classes or series of preferred stock, including voting
rights, dividend rights and preferences over the common stock with
respect to dividends or upon the liquidation, dissolution or
winding-up of its business, and other terms. The Company
has issued preferred stock that has a preference over the common
stock with respect to the payment of dividends or upon liquidation,
dissolution or winding-up, and with respect to voting rights.
In accordance with that and with the issuance of preferred stock
the voting rights the common stockholders voting rights have been
diluted and it is possible that the rights of holders of the common
stock or the value of the common stock have been adversely
affected.
The Company does not expect to pay any dividends on common stock
for the foreseeable future.
The Company has not paid any cash dividends on its
common stock to date and does not anticipate it will pay cash
dividends on its common stock in the foreseeable
future. Accordingly, stockholders must be prepared to rely
on sales of their common stock after price appreciation to earn an
investment return, which may never occur. Any
determination to pay dividends in the future will be made at the
discretion of the Company’s board of directors and will
depend on the Company’s results of operations, financial
conditions, contractual restrictions, restrictions imposed by
applicable law, and other factors that the Company’s board
deems relevant.
FINRA sales practice requirements may also limit your ability to
buy and sell our common stock, which could depress the price of our
shares.
Financial Industry Regulatory Authority, Inc.
(“FINRA”) rules require broker-dealers to have
reasonable grounds for believing that an investment is suitable for
a customer before recommending that investment to the customer.
Prior to recommending speculative low-priced securities to their
non-institutional customers, broker-dealers must make reasonable
efforts to obtain information about the customer’s financial
status, tax status and investment objectives, among other things.
Under interpretations of these rules, FINRA believes that there is
a high probability such speculative low-priced securities will not
be suitable for at least some customers. Thus, FINRA requirements
make it more difficult for broker-dealers to recommend that their
customers buy our common stock, which may limit your ability to buy
and sell our shares, have an adverse effect on the market for our
shares, and thereby depress our share price.
-14-
RISKS RELATED TO THIS OFFERING
Purchasers in this Offering will experience immediate and
substantial dilution in the book value of their
investment.
If we successfully sell all securities registered
by this offering and investors exercise all warrants included in
this offering, new investors will own approximately % of our
outstanding common stock. In addition, we have issued options,
warrants or other derivative securities to acquire common stock at
prices below the public offering price. To the extent outstanding
options, warrants or other derivative securities are ultimately
exercised or converted, or if we issue restricted stock to our
employees under our equity incentive plans, there will be further
dilution to investors who purchase shares in this offering. In
addition, if we issue additional equity securities or derivative
securities, investors purchasing shares in this offering will
experience additional dilution. For a further description of the
dilution that you will experience immediately after this offering,
see “Dilution.”
We may allocate the net proceeds from this Offering in ways that
differ from our estimates based on our current plans and
assumptions discussed in the section titled "Use of Proceeds" and
with which you may not agree.
The allocation of net proceeds of the offering set
forth in the “Use of
Proceeds” section of this
prospectus represents our estimates based upon our current plans
and assumptions regarding industry and general economic conditions,
our future revenues and expenditures. The amounts and timing of our
actual expenditures will depend on numerous factors, including
market conditions, cash generated by our operations, business
developments and related rate of growth. We may find it necessary
or advisable to use portions of the proceeds from this offering for
other purposes. Circumstances that may give rise to a change in the
use of proceeds and the alternate purposes for which the proceeds
may be used are discussed in the section in this prospectus
entitled “Use of
Proceeds”. You may not
have an opportunity to evaluate the economic, financial or other
information on which we base our decisions on how to use our
proceeds. As a result, you and other stockholders may not agree
with our decisions. See “Use of
Proceeds” for additional
information.
The warrants are speculative in nature.
The
warrants offered by us in this offering do not confer any rights of
ownership of shares of common stock on its holders, such as voting
rights or the right to receive dividends, but only represent the
right to acquire shares of common stock at a fixed price for a
limited period of time. Specifically, commencing on the date of
issuance, holders of the warrants may exercise their right to
acquire the shares of common stock and pay an expected exercise
price of $ per share, subject to adjustment upon certain events,
prior to years from the date of issuance, after which date any
unexercised warrants will expire and have no further
value.
There is no established public trading market for the warrants
being offered in this offering and we do not intend to apply to
list the warrants on a securities exchange or automated quotation
system.
There
is no established public trading market for the warrants being
offered in this offering. We do not intend to apply to list the
warrants on a securities exchange or automated quotation system.
Without an active trading market, the liquidity of warrants will be
limited.
-15-
SPECIAL NOTE REGARDING FORWARD-LOOKING INFORMATION
This prospectus includes forward-looking statements. All
statements, other than statements of historical fact, contained in
this prospectus, including statements regarding our future
operating results, financial position and cash flows, our business
strategy and plans and our objectives for future operations, are
forward-looking statements. In some cases, you can identify
forward-looking statements by terms such as “believe,”
“may,” “will,” “estimate,”
“continue,” “anticipate,”
“plan,” “target,” “project,”
“contemplate,” “predict,”
“potential,” “would,” “could,”
“should,” “intend” and “expect”
or the negative of these terms or other similar
expressions.
We have based these forward-looking statements
largely on our current expectations and projections about future
events and financial trends that we believe may affect our
financial condition, operating results, business strategy,
short-term and long-term business operations and objectives. These
forward-looking statements speak only as of the date of this
prospectus and are subject to a number of risks, uncertainties and
assumptions, including those described under sections in this
prospectus entitled “Risk
Factors” and
“Management’s Discussion
and Analysis of Financial Condition and Results of
Operations” and elsewhere
in this prospectus. Moreover, we operate in a very competitive and
rapidly changing environment. New risk factors and uncertainties
may emerge from time to time. It is not possible for our management
to predict all risk factors and uncertainties, nor can we assess
the impact of all factors on our business or the extent to which
any factor, or combination of factors, may cause actual results to
differ materially from those contained in any forward-looking
statements we may make. In light of these risks, uncertainties and
assumptions, the future events and trends discussed in this
prospectus may not occur and actual results could differ materially
and adversely from those anticipated or implied in the
forward-looking statements.
You
should not rely upon forward-looking statements as predictions of
future events. Although we believe that the expectations reflected
in the forward-looking statements are reasonable, we cannot
guarantee that the future results, levels of activity, performance
and events and circumstances reflected in the forward-looking
statements will be achieved or occur. Moreover, neither we nor any
other person assume responsibility for the accuracy and
completeness of the forward-looking statements. Except as required
by applicable law, we undertake no obligation to update publicly or
revise any forward-looking statements for any reason after the date
of this prospectus to conform these statements to actual results or
to changes in our expectations, whether as a result of any new
information, future events, changed circumstances or
otherwise.
This
prospectus contains estimates and statistical data that we obtained
from industry publications and reports. These publications
generally indicate that they have obtained their information from
sources believed to be reliable, but do not guarantee the accuracy
and completeness of their information, and you are cautioned not to
give undue weight to such estimates. Although we believe the
publications are reliable, we have not independently verified their
data. In addition, projections, assumptions and estimates of our
future performance and the future performance of the markets in
which we operate are necessarily subject to a high degree of
uncertainty and risk.
-16-
USE OF PROCEEDS
We estimate that the net proceeds to us from the
sale of the securities that we are offering will be approximately $
million, based upon the assumed public offering price of $
per share and associated warrant, which is
the last reported bid price of our common stock on the OTC
Pink Marketplace on
, 2017, after deducting estimated
offering expenses payable by us and excluding any proceeds from the
potential exercise of warrants offered hereby, if
any.
Each
$0.10 increase (decrease) in the assumed public offering price of $
per share would increase (decrease) the net
proceeds to us from this offering by $ million, assuming the number
of shares offered by us, as set forth on the cover page of this
prospectus, remains the same, and after deducting the estimated
commissions and estimated offering expenses payable by us. We may
also increase or decrease the number of shares we are offering.
Each increase (decrease) of 200,000 shares in the number of shares
offered by us would increase (decrease) the net proceeds to us from
this offering by approximately $ million, assuming that the public
offering price stays the same, and after deducting the estimated
commissions and the estimated offering expenses payable by
us.
The principal purposes of this offering are to raise additional
working capital, and increase our public float. We currently intend
to use the net proceeds we receive from this offering for working
capital and general corporate purposes, including sales and
marketing activities, product development and capital expenditures.
We may also use a portion of the net proceeds for the acquisition
of, or investment in, technologies, solutions or businesses.
However, we have no present binding commitments or agreements to
enter into any acquisitions or investments. As of December 31,
2016, we had convertible debt totaling $979 thousand which, if not
converted prior to their maturity dates in May 2017, will be due
and payable at that time plus any accrued interest. We may be
required to use a portion of the net proceeds to pay such debt if
outstanding at maturity. Pending these uses, we intend to invest
the net proceeds from this offering in short-term, investment-grade
interest-bearing securities such as money market accounts,
certificates of deposit, commercial paper and guaranteed
obligations of the U.S. government.
The amounts and timing of our actual expenditure,
including expenditure related to sales and marketing and product
development will depend on numerous factors, including the status
of our product development efforts, our sales and marketing
activities, the amount of cash generated or used by our operations,
competitive pressures and other factors described under
“Risk
Factors” in this
prospectus. We therefore cannot estimate the amount of net proceeds
to be used for the purposes described above. As a result, we may
find it necessary or advisable to use the net proceeds for other
purposes. Our management will have broad discretion in the
application of the net proceeds, and investors will be relying on
our judgment regarding the application of the net proceeds from
this offering.
-17-
PRICE RANGE FOR OUR COMMON EQUITY AND RELATED STOCKHOLDERS
MATTERS
Our
common stock is quoted on the OTC Pink Marketplace under the symbol
“ADMD.” The last closing bid price of our common stock
was $0.14 on February 28,
2017.
The
high and low bid prices of our common stock for the periods
indicated are set forth below. These prices do not
reflect retail mark-up, markdown or commissions. Such OTC PINK
quotations reflect inter-dealer prices, without markup, markdown or
commissions and, particularly because our common stock is traded
infrequently, may not necessarily represent actual transactions or
a liquid trading market.
|
High
|
Low
|
|
|
|
2017
|
|
|
Quarter ending
March 31 (through March 7, 2017)
|
$0.18
|
$0.10
|
|
|
|
2016
|
|
|
Quarter ended
December 31
|
$0.24
|
$0.07
|
Quarter ended
September 30
|
$0.40
|
$0.14
|
Quarter ended June
30
|
$0.96
|
$0.20
|
Quarter ended March
31
|
$0.96
|
$0.07
|
|
|
|
2015
|
|
|
Quarter ended
December 31
|
$0.48
|
$0.11
|
Quarter ended
September 30
|
$0.49
|
$0.05
|
Quarter ended June
30
|
$0.19
|
$0.03
|
Quarter ended March
31
|
$0.27
|
$0.03
|
Holders
As of
December 31, 2016, we had 31,743,797 shares of common stock, $0.001
par value, issued and outstanding held by approximately 200
shareholders of record. Our transfer agent is American
Registrar & Transfer Co., 1234 W South Jordan Pkwy Ste B3,
South Jordan, UT 84095.
-18-
DIVIDENDS
The
Company has not paid any cash dividends on its common stock to date
and do not anticipate it will pay cash dividends on its common
stock in the foreseeable future. The payment of
dividends in the future will be contingent upon revenues and
earnings, if any, capital requirements, and its general financial
condition. The payment of any dividends will be within
the discretion of the board of directors. It is the
present intention of the board of directors to retain all earnings,
if any, for use in the business operations. Accordingly,
the board does not anticipate declaring any dividends on its common
stock in the foreseeable future.
-19-
CAPITALIZATION
The following table sets forth our capitalization as of December
31, 2016 that is derived from our financial information included
elsewhere in this prospectus:
●
on an
actual basis; and
●
on a
pro forma basis, giving effect to the sale and issuance by us of
shares of common and warrants to purchase up
to shares of common
stock in this offering, at an offering price of $ per share and
associated warrant, and after deducting estimated offering expenses
payable by us.
|
December 31, 2016
|
|
|
Actual
|
As Adjusted
|
|
|
|
|
|
|
Cash and cash
equivalent
|
$27,889
|
$
|
Debt:
|
|
|
Accounts payable
and accrued expenses
|
$1,137,086
|
|
Related part
accounts payable
|
109,718
|
|
Accrued interest
payable
|
114,755
|
|
Payroll liabilities
payable
|
499,502
|
|
Convertible notes
payable, net
|
544,508
|
|
Derivative
liability
|
324,532
|
|
Related party
promissory note
|
332,195
|
|
Total
debt
|
3,062,296
|
|
|
|
|
Stockholders’
Equity (Deficit):
|
|
|
Common stock,
$0.001 par value; 20,000,000,000 shares authorized; 31,743,797
shares issued and outstanding,
actual;
|
31,744
|
|
Additional paid-in
capital
|
40,672,825
|
|
Accumulated
deficit
|
(57,869,440)
|
|
Total
stockholders’ equity (deficit)
|
(17,164,871)
|
|
Total
capitalization
|
$41,996
|
|
Common
stock outstanding in the table above excludes the following shares
as of December 31, 2016:
●
1,939,062
shares of common stock issuable upon the exercise of stock options
outstanding as of December 31, 2016, at a weighted average exercise
price of $0.81 per share;
●
3,579,505 shares of
common stock issuable upon the exercise of warrants outstanding as
of December 31, 2016, at a weighted average exercise price of $4.45
per share;
●
4,989,395 shares of
common stock issuable upon the conversion of Series A Preferred;
and
●
shares of common
stock issuable upon exercise of warrants to be issued in connection
with this offering.
-20-
DILUTION
If
you invest in our common stock in this offering, your ownership
interest will immediately be diluted to the extent of the
difference between the amount per share paid by purchasers of
shares of our common stock in this offering and the as adjusted net
tangible book value (deficit) per share of our common stock
immediately after this offering.
As of December 31, 2016, our historical net
tangible book value (deficit) was approximately $3.0
million, or $0.10 per
share of our common stock. Net tangible book value (deficit) per
share represents the amount of our total tangible assets less our
total liabilities, divided by the number of shares of our common
stock outstanding as of December 31, 2016.
After giving further effect to our sale of
shares of our common stock in this offering at an
assumed public offering price of $ per share, which is the last
reported bid price of our common stock on the OTC Pink Marketplace
on March 7, 2017, and after deducting the estimated offering
expenses payable by us, our as adjusted net tangible book value
(deficit) as of December 31, 2016 would have been approximately $
million, or
approximately $ per share of our common stock. This represents an
immediate increase in as adjusted net tangible book value of $ per
share to existing stockholders and an immediate dilution of $ per
share to new investors purchasing shares of our common stock in
this offering. The following table illustrates this
dilution:
Assumed public
offering price per share
|
|
$ |
|
|
|
Net tangible book
value (deficit) per share as of December 31, 2016
|
$
|
|
|
|
|
Increase per share
attributable to new investors in this offering
|
|
|
|
|
|
As adjusted net
tangible book value (deficit) per share after this
offering
|
|
|
|
|
|
Dilution per share
to new investors in this offering
|
|
$
|
Each
$0.10 increase (decrease) in the assumed public offering price of $
per share, which is last reported sale price of our common stock on
the OTC Pink Marketplace on March , 2017, would increase (decrease)
our as adjusted net tangible book value (deficit) by $
per share and the dilution in as adjusted net tangible
book value (deficit) per share to new investors in this offering by
$ per share, assuming the number of shares offered by
us, as set forth on the cover page of this prospectus, remains the
same, and after deducting the estimated commissions and estimated
offering expenses payable by us.
We
may also increase or decrease the number of shares we are offering.
An increase of 200,000 shares in the number of shares offered by us
would increase our as adjusted net tangible book value (deficit) by
$ per share and decrease the dilution to new
investors in this offering by approximately $ per
share, assuming that the assumed public offering price remains the
same, and after deducting the estimated commissions and the
estimated offering expenses payable by us. Similarly, a decrease of
200,000 shares in the number of shares offered by us would
decrease our as adjusted net tangible book value (deficit) by $
per share and increase the dilution to new
investors in this offering by approximately $ per
share, assuming that the public offering price remains the same,
and after deducting the estimated discounts and commissions and the
estimated offering expenses payable by us.
The
foregoing table and discussion is based on 31,743,797 shares of our
common stock outstanding as of December 31, 2016 and excludes the
following, in each case as of such date:
●
1,939,062
shares of common stock issuable upon the exercise of stock options
outstanding as of December 31, 2016, at a weighted average exercise
price of $0.81 per share;
●
3,579,505 shares of
common stock issuable upon the exercise of warrants outstanding as
of December 31, 2016, at a weighted average exercise price of $4.45
per share;
●
4,989,395 shares of
common stock issuable upon the conversion of Series A Preferred;
and
●
shares
of common stock issuable upon exercise of warrants to be issued in
connection with this offering.
To
the extent that any of the outstanding options or warrants to
purchase shares of our common stock are exercised, new investors
may experience further dilution. In addition, we may issue
additional shares of common stock, other equity securities or
convertible debt securities in the future, which may cause further
dilution to new investors in this offering.
-21-
MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL
CONDITION
AND RESULTS OF OPERATIONS
The following discussion and
analysis is intended as a review of significant factors affecting
the Company’s financial condition and results of operations
for the periods indicated. The discussion should be read
in conjunction with the Company’s financial statements and
the notes presented herein. In addition to historical
information, the following Management’s Discussion and
Analysis of Financial Condition and Results of Operations contains
forward-looking statements that involve risks and uncertainties.
The Company’s actual results could differ significantly from
those anticipated in these forward-looking statements as a result
of the risk factors set forth above and other factors discussed in
this prospectus.
Comparison
for the Year Ended December 31, 2016 and December 31,
2015
The
following table sets forth information from the Company’s
statements of operations for the years ended December 31, 2016
and 2015.
|
Year Ended
December 31, 2016
|
Year Ended
December 31, 2015
|
Revenues
|
$8,108
|
$24,108
|
|
|
|
Operating
expense
|
4,444,578
|
2,065,371
|
|
|
|
Operating
loss
|
(4,436,470)
|
(2,041,263)
|
|
|
|
Non-operating
income (expense)
|
(5,418,425)
|
8,273,949
|
|
|
|
Net income
(loss)
|
$(9,854,895)
|
$6,232,686
|
Revenue
Consulting revenue
was $8,108 and $24,108 for the years ended December 31, 2016 and
2015, respectively. Consulting revenue consists of
providing the Company with assistance in strategic targetry
services, and research into production of radiophamaceuticals and
the operations of radioisotope production facilities.
Operating Expense
Operating expense
for the twelve months ended December 31, 2016 and 2015 consists of
the following:
|
Twelve months ended
December 31, 2016
|
Twelve months ended
December 31, 2015
|
Cost of
materials
|
$-
|
$474
|
Sales and marketing
expense
|
284,138
|
-
|
Depreciation and
amortization expense
|
2,947
|
5,672
|
Professional
fees
|
2,068,796
|
741,375
|
Stock options and
warrants granted
|
675,324
|
80,635
|
Payroll
expense
|
652,877
|
679,259
|
Research and
development
|
328,026
|
149,650
|
General and
administrative expense
|
432,470
|
408,306
|
|
$4,444,578
|
$2,065,371
|
Operating expense
for the twelve months ended December 31, 2016 and 2015 was
$4,444,578 and $2,065,371, respectively. The increase in operating
expense from 2015 to 2016 is largely attributable to professional
fees ($2,068,796 for the twelve months ended December 31, 2016
versus $741,375 for the twelve months ended December 31, 2015). The
increase in professional fees was due to hiring consultants to
assist in raising capital to pay off debt and for operating
expenses.
-22-
The
increase in operating expense from 2015 to 2016 can also be
attributed to research and development ($328,026 for the twelve
months ended December 31, 2016 versus $149,650 for the twelve
months ended December 31, 2015), and stock options granted and
warrant expense ($675,324 for the twelve months ended December 31,
2016 versus $80,635 for the twelve months ended December 31,
2015).
Non-Operating Income (Expense)
Non-Operating
income (expense) for the twelve months ended December 31, 2016 and
2015 consists of the following:
|
Twelve months
ended December 31, 2016
|
Twelve months
ended December 31, 2015
|
Interest
expense
|
$(6,259,467)
|
$(3,196,153)
|
Net gain (loss) on
settlement of debt
|
3,108,342
|
3,562,067
|
Recognized income
from grants
|
21,010
|
21,010
|
Gain (loss) on
derivative liability
|
(2,244,353)
|
7,887,025
|
Loss on impaired
assets
|
(43,957)
|
-
|
|
|
|
|
$(5,418,425)
|
$8,273,949
|
Non-operating
income (expense) for the twelve months ended December 31, 2016
varied from the twelve months ended December 31, 2015 primarily due
to the difference in the gain (loss) on derivative liability of
$10,131,378 (a $7,887,025 gain on derivative liability in 2015
versus a $2,244,353 loss on derivative liability in 2016).
Additionally, there was an increase in interest expense of
$3,063,314, attributable to loan fees incurred ($5,098,094 for the
twelve months ended December 31, 2016 versus $536,347 for the
twelve months ended December 31, 2015).
Income from Grants
On
September 1, 2015, the Company received notification that it had
been awarded from Washington State University $42,019 grant funds
from the sub-award project entitled “Optimized Injectable
Radiogels for High-dose Therapy of Non-Resectable Solid
Tumors”. The Company received $21,010 of the total grant
award in December 2015 and $21,009 of the total grant award in
October 2016.
Net Loss
The
Company’s net income (loss) for the twelve months ended
December 31, 2016 and 2015 was $(9,854,895) and $6,232,686,
respectively, as a result of the items described
above.
Liquidity and Capital Resources
At
December 31, 2016, the Company had negative working capital of
$3,022,417, as compared to $9,755,128 at December 31,
2015. During the twelve months ended December 31, 2016,
the Company experienced negative cash flow from operations of
$1,926,713 and it expended $0 for investing activities while adding
$1,775,570 of cash flows from financing activities. As
of December 31, 2016, the Company had $0 commitments for capital
expenditures.
Cash
used in operating activities increased from $1,193,105 for the
twelve-month period ending December 31, 2015 to $1,926,713 for
the twelve-month period ending December 31, 2016. Cash
used in operating activities was primarily a result of the
Company’s non-cash items, such as loss from operations, loss
on preferred and common stock and stock options and warrants issued
for services and other expenses, offset by the net gain and the
gain realized from derivative liabilities and settlement of debt,
preferred stock converted to common stock, and the penalties
resulting from short term debt. Cash provided from financing
activities increased from $1,371,934 for the twelve month period
ending December 31, 2015 to $1,775,570 for the twelve month period
ending December 31, 2016. The increase in cash provided from
financing activities was primarily a result of increase in proceeds
from related party notes, shareholder advances, and sale of
preferred shares.
-23-
The
Company has generated material operating losses since inception.
The Company had a net income of $6,232,686 for the twelve months
ended December 31, 2015, and a net loss of $9,854,895 for the
twelve months ended December 31, 2016. The Company expects to
continue to experience net operating losses. Historically, the
Company has relied upon investor funds to maintain its operations
and develop the Company’s business. The Company anticipates
raising additional capital within the next twelve months for
working capital as well as business expansion, although the Company
can provide no assurance that additional capital will be available
on terms acceptable to the Company, if at all. If the Company is
unable to obtain additional financing to meet its working capital
requirements, it may have to curtail its business or cease all
operations.
The
Company requires funding of at least $1.5 million per year to
maintain current operating activities. Over the next 12 to 24
months, the Company believes it will cost approximately $5.0
million to $10.0 million to fund: (1) the FDA approval process and
initial deployment of RadioGelTM and other
brachytherapy products, and (2) initiate regulatory approval
processes outside of the United States. The continued deployment of
the Company’s brachytherapy products, including
RadioGelTM, and a worldwide
regulatory approval effort will require additional resources and
personnel. The principal variables in the timing and
amount of spending for the brachytherapy products in the next 12 to
24 months will be the FDA’s classification of the
Company’s brachytherapy products as Class II or Class III
devices (or otherwise) and any requirements for additional studies,
which may possibly include clinical studies. Thereafter,
the principal variables in the amount of the Company’s
spending and its financing requirements would be the timing of any
approvals and the nature of the Company’s arrangements with
third parties for manufacturing, sales, distribution and licensing
of those products and the products’ success in the U.S. and
elsewhere. The Company intends to fund its activities through
strategic transactions such as licensing and partnership agreements
or additional capital raises.
Although the
Company is seeking to raise additional capital and has engaged in
numerous discussions with investment bankers and investors, the
Company has not received firm commitments for the required funding.
Based upon its discussions, the Company anticipates that if the
Company is able to obtain the funding required to retire
outstanding debt, pay past due payables and maintain its current
operating activities, that the terms thereof will be materially
dilutive to existing shareholders.
Recent
geopolitical events, including the inherent instability and
volatility in global capital markets, as well as the lack of
liquidity in the capital markets, could impact the Company’s
ability to obtain financing and its ability to execute its business
plan.
Contractual
Obligations (payments due by period as of December 31,
2016)
Contractual
Obligation
|
Total Payments
Due
|
Less than 1
Year
|
1-3
Years
|
3-5
Years
|
More
than
5 Years
|
License Agreement
with Battelle Memorial Institute
|
$100,000
|
$25,000
|
$25,000
|
$25,000 $
|
25,000 per year
|
Effective March
2012, the Company entered into an exclusive license agreement with
Battelle Memorial Institute regarding the use of its patented
RadioGel™ technology. This license agreement calls for a
$17,500 nonrefundable license fee and a royalty based on a percent
of gross sales for licensed products sold; the license agreement
also contains a minimum royalty amount to be paid each year
starting with 2013.
Off-Balance
Sheet Arrangements
The
Company does not have any off balance sheet arrangements that are
reasonably likely to have a current or future effect on the
Company’s financial condition, revenues, results of
operations, liquidity or capital expenditures.
-24-
Accounting
Policies
Use of Estimates
The
preparation of financial statements in accordance with generally
accepted accounting principles requires management to make
estimates and assumptions that affect the reported amounts of
assets and liabilities and the disclosure of contingent assets and
liabilities at the date of financial statements and the reported
amounts of revenues and expenses during the reporting
period. Actual results could differ from those
estimates.
Fixed
Assets
Fixed
assets are carried at the lower of cost or net realizable value.
Production equipment with a cost of $2,500 or greater and other
fixed assets with a cost of $1,500 or greater are capitalized.
Major betterments that extend the useful lives of assets are also
capitalized. Normal maintenance and repairs are charged to expense
as incurred. When assets are sold or otherwise disposed of, the
cost and accumulated depreciation are removed from the accounts and
any resulting gain or loss is recognized in
operations.
Depreciation is
computed using the straight-line method over the following
estimated useful lives:
Production
equipment:
|
3 to 7
years
|
Office
equipment:
|
2 to 5
years
|
Furniture
and fixtures:
|
2 to 5
years
|
Leasehold
improvements and capital lease assets are amortized over the
shorter of the life of the lease or the estimated life of the
asset.
Management of the
Company reviews the net carrying value of all of its equipment on
an asset by asset basis whenever events or changes in circumstances
indicate that its carrying amount may not be recoverable. These
reviews consider the net realizable value of each asset, as
measured in accordance with the preceding paragraph, to determine
whether impairment in value has occurred, and the need for any
asset impairment write-down.
License
Fees
License
fees are stated at cost, less accumulated amortization.
Amortization of license fees is computed using the straight-line
method over the estimated economic useful life of the
asset.
The
Company periodically reviews the carrying values of capitalized
license fees and any impairments are recognized when the expected
future operating cash flows to be derived from such assets are less
than their carrying value.
-25-
Patents
and Intellectual Property
The
Company had a total $35,482 of capitalized patents and intellectual
property costs at December 31, 2015 for the patent rights in the
area of a Brachytherapy seed with a Fast-dissolving Matrix for
Optimized Delivery of Radionuclides. Effective December 31, 2016
the Company agreed to terminate this non-utilized patent license
for which the $35,482 of capitalized patent and intellectual costs
applied and therefore the Company wrote off $35,482 of capitalized
costs in the twelve months ending December 31, 2016.
While
patents are being developed or pending, they are not being
amortized. Management has determined that the economic
life of the patents to be ten years and amortization, over such
10-year period and on a straight-line basis will begin once the
patents have been issued and the Company begins utilization of the
patents through production and sales, resulting in
revenues.
The
Company evaluates the recoverability of intangible assets,
including patents and intellectual property on a continual basis.
Several factors are used to evaluate intangibles, including, but
not limited to, management’s plans for future operations,
recent operating results and projected and expected undiscounted
future cash flows.
Revenue
Recognition
The
Company recognized revenue related to product sales when (i)
persuasive evidence of the arrangement exists, (ii) shipment has
occurred, (iii) the fee is fixed or determinable, and (iv)
collectability is reasonably assured.
Revenue
for the fiscal years ended December 31, 2016 and 2015 consisted of
consulting revenue. The Company recognizes revenue as consulting
services have been performed. Prepayments, if any, received from
customers prior to the services being performed are recorded as
deferred revenue. In these cases, when the services are performed,
the amount recorded as deferred revenue is recognized as revenue.
The Company does not accrue for sales returns and other allowances
as it has not experienced any returns or other
allowances.
Income
from Grants and Deferred Income
Government grants
are recognized when all conditions of such grants are fulfilled or
there is reasonable assurance that they will be fulfilled. The
Company has chosen to recognize income from grants as it incurs
costs associated with those grants, and until such time as it
recognizes the grant as income those funds received will be
classified as deferred income on the balance sheet.
Net
Income (Loss) Per Share
The
Company accounts for its income (loss) per common share by
replacing primary and fully diluted earnings per share with basic
and diluted earnings per share. Basic earnings/loss per share is
computed by dividing income (loss) available to common stockholders
(the numerator) by the weighted-average number of common shares
outstanding (the denominator) for the period, and does not include
the impact of any potentially dilutive common stock equivalents.
The computation of diluted earnings per share is similar to basic
earnings per share, except that the denominator is increased to
include the number of additional common shares that would have been
outstanding if potentially dilutive common shares had been
issued.
-26-
Research
and Development Costs
Research and
developments costs, including salaries, research materials,
administrative expenses and contractor fees, are charged to
operations as incurred. The cost of equipment used in research and
development activities which has alternative uses is capitalized as
part of fixed assets and not treated as an expense in the period
acquired. Depreciation of capitalized equipment used to perform
research and development is classified as research and development
expense in the year computed.
Income
Taxes
To
address accounting for uncertainty in tax positions, the Company
clarifies the accounting for income taxes by prescribing a minimum
recognition threshold that a tax position is required to meet
before being recognized in the financial statements. The Company
also provides guidance on de-recognition, measurement,
classification, interest, and penalties, accounting in interim
periods, disclosure and transition.
The
Company files income tax returns in the U.S. federal jurisdiction,
and Delaware.
Interest costs and
penalties related to income taxes, if any, will be classified as
interest expense and general and administrative costs,
respectively, in the Company’s financial statements. For the
years ended December 31, 2016 and 2015, the Company did not
recognize any interest or penalty expense related to income taxes.
The Company believes that it is not reasonably possible for the
amounts of unrecognized tax benefits to significantly increase or
decrease within the next 12 months.
Fair
Value of Financial Instruments
The
Company adopted ASC Topic 820 (originally issued as SFAS 157,
“Fair Value
Measurements”) as of January 1, 2008 for financial
instruments measured as fair value on a recurring basis. ASC Topic
820 defines fair value, established a framework for measuring fair
value in accordance with accounting principles generally accepted
in the United States and expands disclosures about fair value
measurements.
-27-
Fair
value is defined as the price that would be received to sell an
asset or paid to transfer a liability in an orderly transaction
between market participants at the measurement date. ASC Topic 820
established a three-tier fair value hierarchy which prioritizes the
inputs used in measuring fair value. The hierarchy gives the
highest priority to unadjusted quoted prices in active markets for
identical assets or liabilities (level 1 measurements) and the
lowest priority to unobservable inputs (level 3 measurements).
These tiers include:
-
Level 1, defined as
observable inputs such as quoted prices for identical instruments
in active markets;
-
Level 2, defined as
inputs other than quoted prices in active markets that are either
directly or indirectly observable such as quoted prices for similar
instruments in active markets or quoted prices for identical or
similar instruments in markets that are not active;
and
-
Level 3, defined as
unobservable inputs in which little or no market data exists,
therefore requiring an entity to develop its own assumptions, such
as valuations derived from valuation techniques in which one or
more significant inputs or significant value drivers are
unobservable.
Stock-Based
Compensation
The
Company recognizes in the financial statements compensation related
to all stock-based awards, including stock options, based on their
estimated grant-date fair value. The Company has estimated expected
forfeitures and is recognizing compensation expense only for those
awards expected to vest. All compensation is recognized by the time
the award vests.
The
Company accounts for equity instruments issued in exchange for the
receipt of goods or services from non-employees. Costs are measured
at the fair market value of the consideration received or the fair
value of the equity instruments issued, whichever is more reliably
measurable. The value of equity instruments issued for
consideration other than employee services is determined on the
earlier of the date on which there first exists a firm commitment
for performance by the provider of goods or services or on the date
performance is complete. The Company recognizes the fair
value of the equity instruments issued that result in an asset or
expense being recorded by the company, in the same period(s) and in
the same manner, as if the Company has paid cash for the goods or
services.
-28-
BUSINESS
In September of 2006, the Company began operating
as Advanced Medical Isotope Corporation (the
“Company”). The Company’s
predecessor was incorporated under the
laws of the state of Delaware in 1994. The Company has authorized
capital of 2,000,000,000 shares of common stock, $0.001 par value
per share, and 20,000,000 shares of preferred stock, $0.001 par
value per share.
Our
principal place of business is 1021 N Kellogg Street, Kennewick,
Washington, 99336. Our telephone number is (509) 736-4000. Our
corporate website address is http://www.isotopeworld.com. Our
common stock is currently listed for quotation on the OTC Pink
Marketplace under the symbol “ADMD.”
Overview
The
Company is a late stage radiation oncology medical device company
engaged in the development of its yttrium-90 based brachytherapy
device, RadioGel™, for the treatment of non-resectable
tumors. A prominent team of radiochemists, scientists and
engineers, collaborating with strategic partners, including
national laboratories, universities and private corporations, lead
the Company’s development efforts. The Company’s
overall vision is to globally empower physicians, medical
researchers and patients by providing them with new isotope
technologies that offer safe and effective treatments for
cancer.
The Company’s current focus is on the
development of its RadioGel™
device. RadioGel™
is an injectable particle-gel, for brachytherapy radiation
treatment of cancerous tumors in people and animals.
RadioGel™
is comprised of a hydrogel, or a substance that is liquid at room
temperature and then gels when reaching body temperature after
injection into a tumor. In the gel are small, one micron,
yttrium-90 phosphate particles (“Y-90”). Once injected, these inert particles are
locked in place inside the tumor by the gel, delivering a very high
local radiation dose. The radiation is beta, consisting of
high-speed electrons. These electrons only travel a short distance
so the device can deliver high radiation to the tumor with minimal
dose to the surrounding tissue. Optimally, patients can go home
immediately following treatment without the risk of radiation
exposure to family members. Since Y-90 has a half-life of 2.7 days,
the radioactively drops to 5% of its original value after ten
days.
The Company’s lead brachytherapy products,
including RadioGel™,
incorporate patented technology developed for Battelle Memorial
Institute (“Battelle”) at Pacific Northwest National Laboratory,
a leading research institute for government and commercial
customers. Battelle has granted the Company an exclusive license to
patents covering the manufacturing, processing and applications of
RadioGelTM
(the “Battelle
License”). Other
intellectual property protection includes proprietary production
processes and trademark protection in 17 countries. The Company
plans to continue efforts to develop new refinements on the
production process, and the product and application hardware, as a
basis for future patents.
The Company is currently focusing on obtaining
approval from the Food and Drug Administration
(“FDA”) to market and sell RadioGel™ as a
Class II medical device. The Company first requested FDA approval
of RadioGel™ in June 2013, at which time the FDA classified
RadioGel™ as a medical device. The Company then followed with
a 510(k) submission which the FDA responded with a request for a
physician letter of substantial equivalence and a reformatted
510(k) summary, which the Company provided January 2014. In
February 2014 the FDA ruled the device as not substantially
equivalent due to a lack of predicate device and it was classified
to Class III. The Company is currently developing test plans to
address issues raised by the FDA in connection with the
Company’s previous submissions regarding RadioGel™,
including developing specific test plans and specific indication of
use. The Company intends to request FDA approval to apply
for de
novo classification of
RadioGel™, which would reclassify the device from a Class III
device to a Class II device, further simplifying the regulatory
path.
In previous FDA submittals, the Company proposed
applying RadioGel™
for a very broad range of cancer therapies, referred to as
Indication for Use. The FDA has requested that the Company reduce
its Indications for Use. To comply with that request, the Company
has expanded its Medical Advisory Board (“MAB”) and engaged doctors from respected
hospitals who have evaluated the candidate cancer therapies based
on three criteria: (1) potential for FDA approval and successful
therapy; (2) notable advantage over current therapies; and (3)
probability of wide spread acceptance by the medical
community.
The
MAB selected eighteen applications for RadioGel™,
each of which meet the criteria described above. This large number
confirms the wide applicability of the device and defines the path
for future business growth. The Company intends to apply to the FDA
for a single Indication for Use, followed by subsequent
applications for additional Indications for Use. The initial
application should facilitate each subsequent application, and the
testing for many of the subsequent applications could be conducted
in parallel, depending on available resources.
-29-
The
MAB selected the treatment of basal cell and squamous cell skin
cancers for the first Indication for Use to be submitted to the
FDA. According to the American Cancer Society, one out of every
three new cancers diagnosed in the U.S. is a cancerous skin lesion
of this type, representing 5.5 million tumors diagnosed annually.
The MAB believes RadioGel™
has the potential to be the preferred treatment in a reasonable
number of cases in a very large market.
The
Company’s, IsoPet Solutions division was established in May
2016 to focus on the veterinary oncology market. The Company has
engaged four different university veterinarian hospitals to begin
using RadioGel™
for treatment of four different cancer types in dogs and cats.
Washington State University Veterinary Hospital has tested one cat
to demonstrate the procedures and the absence of any significant
toxicity effect. The other three centers are expected to begin
therapy during the second quarter of 2017 after their internal
administrative review process is completed.
These
animal therapies will focus on creating labels that describe the
procedures in detail as a guide to future veterinarians. The labels
will be voluntarily submitted to the FDA for review. They will then
be used as data for future FDA applications in the medical sector
and as key intellectual property for licensing to private
veterinary clinics. In 2018, Dr. Alice Villalobos, the Chair of our
Veterinarian Advisory Board, will be the first licensee of these
therapies in her private clinic to demonstrate the business
model.
The
Company anticipates that future profit will be derived from direct
sales of RadioGel™
and related services, and from licensing to private medical and
veterinary clinics in the U.S. and internationally.
Financing and Strategy
Research
and development of RadioGel™
and other products in the Company’s brachytherapy product
line has been funded with proceeds from the sale of equity and debt
securities as well as a series of grants. The Company requires
funding of approximately $1.5 million annually to maintain current
operating activities. Over the next 12 to 24 months, the Company
believes it will cost approximately $5.0 million to $10.0 million
to fund: (1) the FDA approval process and initial deployment of
RadioGel™
and other brachytherapy products, and (2) initiate regulatory
approval processes outside of the United States. The continued
deployment of RadioGel™
and the Company’s other brachytherapy products and a
worldwide regulatory approval effort will require additional
resources and personnel. The principal variables in the timing and
amount of spending for the brachytherapy products in the next 12 to
24 months will be the FDA’s classification of the
Company’s brachytherapy products, including
RadioGel™,
as Class II or Class III devices (or otherwise) and any
requirements for additional studies which may possibly include
clinical studies. Thereafter, the principal variables in the amount
of the Company’s spending and its financing requirements
would be the timing of any approvals and the nature of the
Company’s arrangements with third parties for manufacturing,
sales, distribution and licensing of those products and the
products’ success in the U.S. and elsewhere. The Company
intends to fund its activities through strategic transactions such
as licensing and partnership agreements or additional capital
raises.
Following
receipt of required regulatory approvals and financing in the U.S.,
the Company intends to outsource material aspects of manufacturing,
distribution, sales and marketing. Outside of the U.S., the Company
intends to pursue licensing arrangements and/or partnerships to
facilitate its global commercialization strategy.
In
the longer-term, subject to the Company receiving adequate funding,
regulatory approval for RadioGel™
and other brachytherapy products, and thereafter being able to
successfully commercialize its brachytherapy products, the Company
intends to consider resuming research efforts with respect to other
products and technologies intended to help improve the diagnosis
and treatment of cancer and other illnesses
Based
on the Company’s financial history since inception, its
auditor has expressed substantial doubt as to the Company’s
ability to continue as a going concern. The Company has limited
revenue, nominal cash, and has accumulated deficits since
inception. If the Company cannot obtain sufficient additional
capital, the Company will be required to delay the implementation
of its business strategy and may not be able to continue
operations.
-30-
Product Features
The
Company’s RadioGel™
device has the following product features:
●
Beta particles only travel a short distance so the
device can deliver high radiation to the tumor with minimal dose to
the nearby normal tissues. In
medical terms Y-90 beta emitter has a high efficacy
rate;
●
Benefitting
from the short penetration distance, the patient can go home
immediately with no fear of exposure to family members, and there
is a greatly reduced radiation risk to the doctor. A simple plastic
tube around the syringe, gloves and safety glasses are all that is
required. Other gamma emitting products require much more
protection;
●
A
2.7-day half-life means that only 5% of the radiation remains after
ten days. This is in contrast to the industry-standard gamma
irradiation product, which has a half-life of 17 days;
●
The
short half-life also means that any medical waste can be stored for
thirty days then disposed as normal hospital waste;
●
RadioGel™
can be administered with small diameter needles (27-gauge) so there
is minimal damage to the normal tissue. This is in contrast to the
injection of metal seeds, which does considerable damage;
and
●
After
about 120 days the gel resorbs by a normal biological cycle, called
the Krebs Cycle. The only remaining evidence of the treatment are
phosphate particles so small in diameter that it requires a
high-resolution microscope to find them. This is in contrast to
permanent presence of metal seeds.
Steps from Production to Therapy
Device Production
During
the next two years, the Company intends to outsource material
aspects of manufacturing and distribution. As future product volume
increases, the Company will reassess its make-buy decision on
manufacturing and will analyze the cost/benefit of a centrally
located facility.
Production of the Hydrogel
RadioGel™
is manufactured with a proprietary process under ventilated sterile
hood by following strict Good Laboratory Practices, or GLP,
procedures. It is made in large batches that are frozen for up to
three months. When the product is ready to ship, a small quantity
of the gel is dissolved in a sterile saline solution. It is then
passed through an ultra-fine filter to ensure
sterility.
Production of the Yttrium-90 Phosphate Particles
The
Y-90 particles are produced with simple ingredients via a
proprietary process, again following strict GLP procedures. They
are then mixed into a phosphate-buffered saline solution. They can
be produced in large batches for several shipments. The number of
particles per shipment is determined by the dose prescribed by the
doctor.
Shipment
RadioGel™
is shipped in two containers, one with a solution of the gel and
the other with a solution of the particles. Before shipment they
are subjected to sterility testing, again by strict procedures. The
vial with the Y-90 is put through a special radiation calibrator,
which measures beta particles. The vials can be shipped via FedEx
or UPS by following the proper protocols.
-31-
At the User
The
user receives the two vials. The solution containing the
RadioGel™
is mixed with the solution containing the Y-90 particles. This is
then shaken to ensure homogeneity and withdrawn into a syringe. The
quantities that are mixed are calculated from the information on
the product label.
The
specific injection technique depends on the Indication for Use. For
small tumors, one centimeter in diameter or less, the cancer is
treated with a single injection. For larger tumors, the cancer is
treated with a series of small injections from the same
syringe.
Principal Markets
The
Company is currently pursuing two synergistic business sectors,
medical and veterinary, each of which are summarized
below.
Medical Sector
Brachytherapy
is the use of radiation to destroy cancerous tumors by placing a
radiation source inside or next to the treatment area. According to
the 2014 MEDraysintell report, the global market for brachytherapy
reached US$ 680 million in 2013 and is projected to reach $2.4
billion by 2030. It is estimated that the U.S. market represents
approximately half of the global market. The Company believes there
are significant opportunities in prostate, breast, liver,
pancreatic, head and neck cancers. The 2014 U.S. estimated new
cases of cancer according to the American Cancer Society are
233,000 prostate, 235,030 breast, 31,190 liver, and 46,420
pancreas.
RadioGel™
is currently fully developed, requiring only FDA approval before
commercialization. The Company has been seeking FDA approval
of RadioGel™
for almost four years. The principal issue preventing approval is
that the Company attempted to obtain regulatory approval for a
broad range of Indications for Use, including all non-resectable
cancers, without sufficient supporting data.
-32-
Building on the FDA’s ruling of
RadioGel™
as a device, the Company is currently developing test plans to
address issues raised in the Company’s prior FDA submittal
regarding RadioGel™.
The Company intends to request FDA approval to submit
RadioGel™
for de
novo classification, which
would reclassify the device from a Class III device to a Class II
device, and accelerate the regulatory approval
path.
After
analyzing the Company’s data and the last four years of
communication from the FDA, the Company has taken the following
steps:
1.
Under
new leadership, the Company is implementing all past
recommendations from the FDA. The Company intends to narrow the
Indications for Use, will provide test plans for FDA review to
respond to answer all previous FDA questions, and will request a
pre-submission meeting;
2.
Prepare a pre-submission request document and FDA
meeting request to obtain feedback on the test plans in order to
initiate testing, to present the proposed content for the final
application and to request permission to submit a
de
novo;
3.
Submit an Investigational Device Exemption
(“IDE”) to obtain permission to conduct human
clinical studies; and
4.
File a de novo or Pre-Market Approval
application.
The
critical path is the required testing – in vitro, animal
testing, human clinical studies – all of which is resource
dependent.
In previous submittals, the Company proposed
applying a very broad range of cancer therapies, referred to as
Indications for Use, to RadioGel™.
The FDA has strongly advised the Company to reduce its Indications
for Use. To comply with that request, the Company has expanded its
MAB, consisting of Drs. Barry D. Pressman (Chairman), Albert
DeNittis, Howard Sandler, and Darrell Fisher.
The MAB
evaluated the candidate cancer
therapies based on three criteria: (i) the potential for FDA
approval and successful therapy; (ii) notable advantages of
RadioGel™
over current therapies; and (iii) the likelihood that
RadioGel™
can be widely accepted by the medical community and profitably
commercialized.
The
MAB selected eighteen Indications for Use for
RadioGel™,
each of which meets the above-mentioned criteria. These eighteen
Indications for Use are listed below. This large number confirms
the wide applicability of the device and defines the path for
future growth. The Company intends to apply to the FDA for a single
Indication for Use, followed by subsequent applications for
additional Indications for Use. The initial application should
facilitate each subsequent application, and the testing for many of
the subsequent applications could be conducted in parallel,
depending on available resources.
● Skin
cancer
● Involved
lymph nodes
● Bladder
● Liver
● Localized
prostate
● Pancreas
● Head
and neck (including sino-nasal and
oropharyngeal)
● Ocular
melanoma
|
● Non-dendritic
brain
● Pediatric
cancers – several types
● Rectal
● Gynecological
● Spinal
● Recurrent
esophageal
● Breast
cancer resection cavity
● Anaplastic
thyroid
|
After
thorough review to prioritize indications, the MAB has selected
basal cell and squamous cell carcinoma (skin cancers) as the first
Indication for Use to be presented to the FDA. According to American Cancer Society, one out of
every three new cancers diagnosed in the U.S. is a cancerous skin
lesion of this type, representing 5.5 million tumors annually. The
MAB believes RadioGel™
will be the preferred treatment in a reasonable number of cases in
a very large market.
-33-
Veterinary Sector
There
are about 150 million pet dogs and cats in the United States.
Nearly one-half of dogs and one-third of cats are diagnosed with
cancer at some point in their lifetime. The Veterinary Oncology
& Hermatology Center in Norwalk, Connecticut, reports that
cancer is the number one natural cause of death in older cats and
dogs, accounting for nearly 50 percent of pet deaths each year. The
American Veterinary Medical Association reports that half of the
dogs ten years or older will die because of cancer. The National
Cancer Institute reports that about six million dogs are diagnosed
with cancer each year, translating to more than 16,000 a day. The
average cost of treating tumors in dogs using radiation is $5,000
to 7,000, according to petcarerx.com.
The Company’s IsoPet operating
division focuses on the veterinary oncology market. Dr.
Alice Villalobos, a founding member of the Veterinary Cancer
Society and the Chair of our Veterinary Medicine Advisory Board,
has been providing guidance to management regarding this
market.
Since
the FDA has classified RadioGel™
as a device, the Company can implement future improvements in the
product and the application techniques to further benefit animals
and to strengthen our intellectual property, without any further
FDA approvals.
The
Company currently intends to utilize university veterinary
hospitals for therapy development, given that veterinary hospitals
offer superior and plentiful veterinarians and students, a large
number of animal patients, radioactive material handling licenses,
and are respected by private veterinary centers and
hospitals.
The Company has recently engaged four different
university veterinarian hospitals to begin using
RadioGel™
for four different cancer types in dogs and cats. Each
veterinary hospital will focus on a different cancer
therapy:
●
Washington State
University – feline sarcoma, possibly followed by canine
sarcoma;
●
University of
Missouri – soft tissue carcinoma, possibly followed by
localized prostate;
●
University of
Florida – lymph nodes, followed by liver cancer;
and
●
Colorado State
University – oral squamous cancer.
Washington State University Veterinary Hospital
has tested one cat to demonstrate the procedures and the absence of
any significant toxicity effect. The others typically take
about two months to complete their internal review before they can
begin therapy. In each case, they will treat several animals with
the objective of creating a detailed therapy procedure, which will
be incorporated into product information for
RadioGel™,
known as a Label. The Company will then voluntarily ask the FDA to
review this Label, as suggested by their guidance.
These
Labels will be used as part of our medical application to the FDA.
A number of these animal cancers also occur in humans, so there is
a direct benefit to our FDA applications when we get to that
particular Indication for Use.
The
Labels and the animal experience will also be used to transfer the
therapies to the private clinics and hospitals. Dr. Villalobos has
agreed that her private clinic will be the first to implement the
Company’s veterinary therapies, and the Company intends to
assist Dr. Villalobos to obtain the required radioactive material
handling license.
After
completing the first set of therapies, each university veterinary
hospital will select additional Indications for Use.
Competitors
The
Company competes in a market characterized by technological
innovation, extensive research efforts, and significant
competition.
The
pharmaceutical and biotechnology industries are intensely
competitive and subject to rapid and significant technological
changes. A number of companies are pursuing the development of
pharmaceuticals and products that target the same diseases and
conditions that our products target. We cannot predict with
accuracy the timing or impact of the introduction of potentially
competitive products or their possible effect on our sales. Certain
potentially competitive products to our products are possibly in
various stages of development. Also, there may be many ongoing
studies with currently marketed products and other developmental
products, which may yield new data that could adversely impact the
use of our products in their current and potential future
Indications for Use. The introduction of competitive products could
significantly reduce our sales, which, in turn would adversely
impact our financial and operating results.
-34-
There
are a wide variety of cancer treatments approved and marketed in
the U.S. and globally. General categories of treatment include
surgery, chemotherapy, radiation therapy and immunotherapy. These
products have a diverse set of success rates and side effects. The
Company’s products, including RadioGel™,
fall into the brachytherapy treatment category. There are a number
of brachytherapy devices currently marketed in the U.S. and
globally. The traditional iodine-125 (I-125) and palladium-103
(Pd-103) technologies for brachytherapy are well entrenched with
powerful market players controlling the market. The
industry-standard I-125-based therapy was developed by Oncura,
which is a unit of General Electric Company. Additionally, C.R.
Bard, a major industry player competes in the I-125 brachytherapy
marketplace. These market competitors are also involved in the
distribution of Pd-103 based products. Cs-131 brachytherapy
products are sold by IsoRay. Several Y-90 therapies have been FDA
approved including SIR-Spheres by Sirtex, TheraSphere by
Biocompatibles UK and Zevalin by Spectrum
Pharmaceuticals.
Raw Materials
The
Company currently manufactures research quantities of brachytherapy
products, including RadioGel™,
or components of these products. The Company obtains supplies,
hardware, handling equipment and packaging from several different
U.S. and foreign suppliers. Some of the products the Company
currently manufactures or intends to manufacture require purchasing
raw materials from a limited number of suppliers, many of which are
international suppliers.
Customers
The
Company anticipates that potential customers for our potential
brachytherapy products likely would include those institutions and
individuals that currently purchase brachytherapy products or other
oncology treatment products.
Government Regulation
The
Company's present and future intended activities in the
development, manufacturing and sale of cancer therapy products,
including RadioGel™,
are subject to extensive laws, regulations, regulatory approvals
and guidelines. Within the U.S., the Company's therapeutic
radiological devices must comply with the U.S. Federal Food, Drug
and Cosmetic Act, enforced by the FDA. The Company is also required
to adhere to applicable FDA Quality System Regulations, also known
as the Good Manufacturing Practices, which include extensive record
keeping and periodic inspections of manufacturing
facilities.
In the
U.S., the FDA regulates, among other things, new product clearances
and approvals to establish the safety and efficacy of these
products. We are also subject to other federal and state laws and
regulations, including the Occupational Safety and Health Act and
the Environmental Protection Act.
-35-
The
Federal Food, Drug, and Cosmetic Act and other federal statutes and
regulations govern or influence the research, testing, manufacture,
safety, labeling, storage, record keeping, approval, distribution,
use, reporting, advertising and promotion of such products.
Noncompliance with applicable requirements can result in civil
penalties, recall, injunction or seizure of products, refusal of
the government to approve or clear product approval applications,
disqualification from sponsoring or conducting clinical
investigations, preventing us from entering into government supply
contracts, withdrawal of previously approved applications, and
criminal prosecution.
In the
United States, a manufacturer of medical devices and devices
utilizing radioactive byproduct material are subject to extensive
regulation by not only federal governmental authorities, such as
the FDA, but also by state and local governmental authorities, such
as the Washington State Department of Health, to ensure such
devices are safe and effective. In Washington State, the Department
of Health, by agreement with the federal Nuclear Regulatory
Commission (“NRC”), regulates the possession,
use, and disposal of radioactive byproduct material as well as the
manufacture of radioactive sealed sources to ensure compliance with
state and federal laws and regulations.
Moreover, any use,
management, and disposal of certain radioactive substances and
wastes are subject to regulation by several federal and state
agencies depending on the nature of the substance or waste
material.
Employees
As
of December 31, 2016, the Company had three full-time personnel.
The Company utilizes several independent contractors to assist with
its operations. The Company does not have a collective bargaining
agreement with any of its personnel, and believes its relations
with its personnel are good.
Description
of Property
The Company is
headquartered in Kennewick, Washington and maintains a lease at a
cost of $1,500 per month from an entity controlled by Carlton M.
Cadwell, Chairman of the Company’s Board of Directors and one
of the Company’s significant shareholders. This lease
initially expired in December 2014, however the Company continues
to rent the space on a month-to-month basis.
Legal Proceedings
On
March 6, 2015, Robert and Maribeth Myers filed a lawsuit against
the Company and BancLeasing, Inc., owner of a linear accelerator
and other equipment leased by the Company, in the Superior Court of
the State of Washington, in and for Benton County (Case No.
15-2-0054101), asserting various claims related to the
Company’s five-year lease of production center space owned by
Mr. and Mrs. Myers. The Company subsequently filed counterclaims
against Mr. and Mrs. Myers, BancLeasing and Washington Trust Bank,
alleging misapplication of lease payments to the principal loan
amount for a linear accelerator and other equipment stored on the
production center property, as well as certain building
improvements made by the Company. During 2016, the Company entered
into a Settlement Agreement with Robert and Maribeth Myers,
pursuant to which the Company agreed to pay a settlement amount of
$438,830 in exchange for the release of all claims related to the
matter, which amount was paid by the Company during the year ended
December 31, 2016.
In
2016, the Company was awarded in the Superior Court of the State of
Washington a total sum of $527,876 against BancLeasing. The Company
is pursuing its options for collection of the awarded amount,
however there can be no assurance as to any eventual
collection.
-36-
MANAGEMENT
Executive Officers and Directors
The
Company’s current directors and executive officers are as
follows:
NAME
|
|
AGE
|
|
POSITION
|
Michael
K. Korenko
|
|
71
|
|
Interim
President and Chief Executive Officer
|
L.
Bruce Jolliff
|
|
67
|
|
Chief
Financial Officer
|
Carlton
M. Cadwell
|
|
72
|
|
Chairman
of the Board and Secretary
|
Thomas
J. Clement
|
|
60
|
|
Director
|
James
C. Katzaroff
|
|
60
|
|
Director
|
Term
of Office
All of
the Company’s directors hold office until the next annual
meeting of the stockholders or until their successors is elected
and qualified. The Company’s executive officers
are appointed by the Company’s board of directors and hold
office until their resignation, removal, death or
retirement.
Background
and Business Experience
The
business experience during the past five years of each of the
Company’s directors and executive officers is as
follows:
Dr. Michael K.
Korenko, interim
President and Chief Executive Officer of the Company since December
2016, joined the Company as an Advisor to the Board of the Company
during 2009 and served as member of the Board from May 2009 to March 2010. Dr.
Korenko has also served on the Hanford Advisory Board since 2009.
Dr. Korenko served as Business Development Manager for
Curtiss-Wright from 2006 to 2009, as Chief Operating Officer for
Curtiss-Wright from 2000 to 2005 and was Executive Vice President
of Closure for Safe Sites of Colorado at Rocky Flats from 1994 to
2000. Dr. Korenko served as Vice President of Westinghouse from
1987 to 1994 and was responsible for the 300 and 400 areas,
including the Fast Flux Testing Facility
(“FFTF”)
and all engineering, safety analysis, and projects for the
Hanford site. Dr. Korenko is the author of 28 patents and has
received many awards, including the National Energy Resources
Organization Research and Development Award, the U.S. Steelworkers
Award for Excellence in Promoting Safety, and the Westinghouse
Total Quality Award for Performance Manager of the Year. Dr.
Korenko has a Doctor of Science from MIT, was a NATO Postdoctoral
Fellow at Oxford University, and was selected as a White House
Fellow for the Department of Defense, reporting to Secretary Cap
Weinberger.
Carlton M.
Cadwell, Chairman of
the Board and Secretary since December 2016, joined the Company as
a director in 2006. Dr. Cadwell brings over 30 years of
experience in business management, strategic planning, and
implementation. He co-founded Cadwell Laboratories, Inc.
in 1979 and has served as its President since its
inception. Cadwell Laboratories, Inc. is a major
international provider of neurodiagnostic medical devices. After
receiving his bachelor’s degree from the University of Oregon
in 1966 and a doctoral degree from the University of Washington in
1970, he began his career serving in the United States Army as a
dentist for three years. From 1973 to 1980, Dr. Cadwell
practiced dentistry in private practice and since has started
several businesses.
Mr.
Cadwell brings to the Board over ten years of service on the Board
and over forty-five years of experience as a successful
entrepreneur, as well as medical expertise.
Leonard Bruce
Jolliff, the Chief
Financial Officer, joined the Company as chief financial officer in
2006. For nine years prior to joining the Company, Mr.
Jolliff was a sole practitioner in the role of CFO for Hire and as
a Forensic Accountant, working with companies ranging from Fortune
500 to small family operations. Mr. Jolliff is a CPA and
a member of the Washington Society of CPAs. He is also a
CFE and a member of the Association of Certified Fraud
Examiners.
Mr. Jolliff has
held CFO and Controller positions in an array of industries and has
worked as a CPA in public practice.
James C.
Katzaroff, a director,
was the Chief Executive Officer of the Company from its inception
in 2006 to December 2016. Mr. Katzaroff is the founder of the
Company. Initially a financial consultant with Wall Street
firms Bateman Eichler, Smith Barney and EF Hutton, Mr. Katzaroff
has been responsible for senior-level corporate strategy, fostering
investment banking relationships, and served as a senior financial
advisor for numerous start-ups and development-stage
companies. From 1998 to 2016, Mr. Katzaroff held senior
positions including Chief Executive Officer, Chief Financial
Officer, Senior Vice President of Finance, Senior Vice President,
and Corporate Secretary of Telemac Corporation, an international
communications company active in the wireless telephony
market. In 2001 he became Chairman and CEO of Apogee
Biometrics, and in 2004 became President of Manakoa Services
Corporation, serving as its interim CEO. He holds a
Bachelor’s Degree in Business Economics from the University
of California, Santa Barbara, and has completed advanced management
courses at the University of Washington.
Mr. Katzaroff brings to the Board experience
working with Wall Street banking firms as well as experience in
numerous start-ups and development-stage
companies.
-37-
Thomas J.
Clement, a director,
joined the Company as a director in 2013. Mr. Clement has over 30
years experience in product development engineering, engineering
management, and senior management. He has participated in two
Company startups through full production. He was responsible for
development of seven novel medical devices through commercial
launch; one device was the leading royalty generator for the
University of Washington for nearly ten years, and in another,
generated revenues of more than $140 million for a leading medical
device company. Mr. Clement since 2013
has held the position of Founder and CEO of Aquaduct Critical Care,
Inc, a private, pre-revenue medical device
company.
Mr.
Clement brings to the Board previous experience in bringing
two startups from development through production as well as
substantial experience in the development of medical
devices.
Identification of Significant Employees and
Consultants
David J. Swanberg, M.S.,
P.E. Chief Technical Officer, has over 30 years’
experience in radiochemical processing, medical isotope production,
nuclear waste management, materials science, regulatory affairs,
and project management. He has worked in diverse organizations
ranging from small start-up businesses to corporations with
multi-billion dollar annual revenues. He previously served as
Executive Vice President of Operations for IsoRay Medical Inc.
managing day-to-day operations, R&D, and New Product
Development. Mr. Swanberg was a co-founder of IsoRay and led the
initial Cs-131 brachytherapy seed product development, FDA 510(k)
submission/clearance, and NRC Sealed Source review and
registration. He led the radiation dosimetry evaluations to meet
American Association of Physicists in Medicine guidelines and is a
current member of the AAPM. Mr. Swanberg served on the IsoRay Board
of Directors and participated in several capital financing rounds
totaling over $30.0 million. He holds a BA in Chemistry from Bethel
University (MN) and an MS in Chemical Engineering from Montana
State University. He has numerous technical publications and holds
several patents.
Fu-Min Su,
Ph.D. was appointed as the Company’s Chief
RadioChemist and Radiation Safety Officer in 2007. With
over 20 years experience in medical isotope R&D and
manufacturing, Dr. Su is also experienced in the area of
coordinating and conducting clinical trials. He has
worked as a senior scientist for a several bio-technology firms,
including NeoRx Corporation from 1987 through
1998, Nycomed-Amersham Imaging in 1999, Bristol-Myers Squibb
from 2000 to 2006, and Cellectar, LLC in 2007, during which time he
developed various radiopharmaceuticals, isotope production methods
and generator systems. Dr. Su has authored a number of
scientific papers, and has written numerous abstracts for the
Journal of Nuclear Medicine. He also holds several
patents relating to radionuclide production and
preparation. Dr. Su received his Ph.D. from the
University of Washington.
Alan E. Waltar,
Ph.D., Chairman of the
Company’s Medical Advisory Board. Dr.
Waltar served as director of Nuclear Energy for the Pacific
Northwest National Laboratory (“PNNL”) in Richland, Washington.
Since 2004, he has continued his affiliation with PNNL as a senior
advisor. Waltar’s other professional appointments include
director of international programs at Advanced Nuclear Medical
Systems; manager of various fast reactor safety and fuels
organizations of Westinghouse Hanford Company; and as professor and
department head of Nuclear Engineering at Texas A&M University.
His other teaching experience includes stints at the Joint Center
for Graduate Study in Richland Washington, the University of
Virginia, and Los Alamos National Laboratory. Formerly the
president of the American Nuclear Society, Dr. Waltar has served on
a number of international nuclear science and radiation panels,
societies, and committees. He is the author of three books: Fast
Breeder Reactors, America the Powerless: Facing Our Nuclear Energy
Dilemma, and Radiation and Modern Life: Fulfilling Marie
Curie’s Dream, and has penned over 70 open literature
papers.
Dr.
Waltar earned his M.S. in Nuclear Engineering from M.I.T. and his
PhD in Engineering Science from the University of California,
Berkeley.
Nigel R. Stevenson,
Ph.D., is a world renowned expert in the production of
medical isotopes. He holds a Ph.D. in Nuclear Physics from the
University of London and has directed many corporate innovations
for imaging and therapeutic nuclide agents. For the past five
years he has served as Chief Operating Officer for Clear Vascular
Inc. and was previously Chief Operating Officer of Trace Life
Sciences, which produced a range of medical radiochemicals and
radiopharmaceuticals. Prior to this, he had been VP Production and
Research for Theragenics Corp. and directed operations in Atlanta
for the world’s largest cyclotron facility (14 cyclotrons)
that produced brachytherapy seeds. Dr. Stevenson was
also Head of Isotope Production and Research at TRIUMF (Canadian
National Accelerator Laboratory) where he managed the production of
medical radioisotopes for MDS Nordion.
Donald A. Ludwig,
Ph.D., Special
Projects Manager and IsoPet Business Development Manager. Dr.
Ludwig is an expert in particle accelerator applications in
radiation therapy, nuclear medicine and radioisotope
production. Since 1988 he has served as an advisor to numerous
entities in the field, both domestic and foreign. Among these
are the Atomic Energy of Canada, the U. S. Department of Energy
Labs at Los Alamos, Berkeley, Fermi, Hanford and Oak Ridge, the
Israel Atomic Energy Agency, the Australian Nuclear Science and
Technology Organization, the Kurchatov Russian Research Institute
in Moscow and the Bhabha Atomic Research Center in Mumbai,
India. He holds a Ph.D. from UCLA in Medical Physics as well
as an MS in Nuclear Physics from Cal Tech, a BS in Physics from the
U. S. Military Academy at West Point and an MBA in Theoretical
Marketing from the University of Southern California.
Section 16(a) Beneficial Ownership Reporting
Compliance
Section
16(a) of the Securities Exchange Act of 1934 requires the
Company’s executive officers, directors and persons who own
more than 10% of the Company’s common stock to file with the
SEC initial reports of beneficial ownership on Form 3, changes in
beneficial ownership on Form 4, and an annual statement of
beneficial ownership on Form 5. Such executive officers,
directors and greater than 10% stockholders are required by SEC
rules to furnish the Company with copies of all such forms that
they have filed.
Based
solely on its review of such forms filed with the SEC and received
by the Company and representations from certain reporting persons,
the Company believes that each of its executive officers and
directors failed to report at least one transaction during the year
ended December 31, 2016.
Code of Ethics
The
Company’s Board of Directors has not adopted a code of ethics
that applies to the principal executive officer, principal
financial officer, principal accounting officer or controller, or
persons performing similar functions, because of the
Company’s limited number of executive officers and employees
that would be covered by such a code and the Company’s
limited financial resources. The Company anticipates
that it will adopt a code of ethics after it increases the number
of executive officers and employees and obtain additional financial
resources.
Audit Committee and Audit Committee Financial Expert
As of
the date of this prospectus,
the Company has not established an audit committee, and therefore,
the Company’s board of directors performs the functions that
customarily would be undertaken by an audit
committee. The Company’s board of directors during
2016 was comprised of three directors, two of whom the Company has
determined satisfied the general independence standards of the
NASDAQ listing requirements.
The
Company’s Board of Directors has determined that none of its
current members qualifies as an “audit committee financial
expert,” as defined by the rules of the SEC. In
the future, the Company intends to establish board committees and
to appoint such persons to those committees as are necessary to
meet the corporate governance requirements imposed by a national
securities exchange, although it is not required to comply with
such requirements until the Company elects to seek listing on a
national securities exchange.
-38-
EXECUTIVE COMPENSATION
The
following table sets forth the compensation paid to the
Company’s Chief Executive Officer and those executive
officers that earned in excess of $100,000 during the twelve month
periods ended December 31, 2016 and 2015 (collectively, the
“Named Executive
Officers”):
Name and Principal Position
|
Year
|
Salary
($)
|
|
Bonus
($)
|
Stock
Awards ($)
|
OptionAwards
($)
|
|
Total
($)
|
|
|
|
|
|
|
|
|
|
Dr. Michael K.
Korenko
|
2016
|
$-
|
(1)
|
$-
|
$-
|
$-
|
|
$-
|
Interim CEO and
President
|
2015
|
$-
|
(1)
|
$-
|
$-
|
$-
|
|
$-
|
|
|
|
|
|
|
|
|
|
James C.
Katzaroff
|
2016
|
$250,000
|
(2)
|
$-
|
$-
|
$408,165
|
(3)
|
$658,165
|
Former CEO and
Chairman
|
2015
|
$250,000
|
(4)
|
$-
|
$-
|
$-
|
|
$250,000
|
|
|
|
|
|
|
|
|
|
L. Bruce
Jolliff
|
2016
|
$180,000
|
|
$-
|
|
$110,389
|
(5)
|
$290,389
|
CFO
|
2015
|
$180,000
|
(6)
|
11,357(7)
|
$-
|
$-
|
|
$190,357
|
(1) Mr.
Korenko began serving as our interim CEO and President on December
14, 2016 and, as such, did not receive any compensation during 2016
or 2015.
(2) Mr.
Katzaroff resigned as Chief Executive Officer in December
2016.
(3) In
June 2016, Mr. Katzaroff received 100,000, three-year common stock
options at $1.00, and 1,000,000, five year common stock options at
$0.50. Additionally Mrs. Katzaroff received 100,000, five-year
common stock options at $0.50, vested equally over 24
months.
(4) Of
this amount, $150,000 was exchanged for 100,000 shares of Series A
Preferred and $75,144 was not paid in 2015, but was accrued as of
December 31, 2015.
(5)
In June 2016, Mr. Jolliff received 240,000, five year common stock
options at $0.50 and another 240,000, five year common stock
options at $0.50 vesting equally over 24 months.
(6) Of
this amount $112,500 was exchanged for 75,000 shares of Series A
Preferred.
(7) Mr.
Jolliff received the additional $11,357 in 2015 to compensate for
additional duties performed that were not originally
contemplated.
Narrative Disclosure to Summary Compensation Table
L. Bruce Jolliff. Mr. Jolliff has a May
2007 employment agreement with the Company that provides for a
salary of $100,000 per year, which amount was increased on January
1, 2012 to $156,000, and again adjusted beginning January 1, 2013
to $180,000. In 2015, Mr. Jolliff received $67,500, and exchanged
$112,500 for 75,000 Series A Preferred shares. In 2016, Mr. Jolliff
received $96,721 and an additional $83,279 was accrued as of
December 31, 2016. The Company may terminate the agreement without
cause at any time upon 30 days’ written
notice. Upon termination, the Company will pay Mr.
Jolliff a severance allowance of two month’s
salary.
James C.
Katzaroff. The Company’s
former Chief Executive Officer, James C. Katzaroff, did not have a
written employment agreement and, therefore, no contracted amount
or schedule of pay. However, his annual compensation was $250,000
and, accordingly, accruals were made for his compensation in 2016
and 2015 to bring his recorded salary to $250,000. In
2016, Mr. Katzaroff received $43,928 and an additional $206,072 was
accrued as of December 31, 2016. In 2015, Mr. Katzaroff received
$24,856, exchanged $150,000 for 100,000 shares of Series A
Preferred, and an additional $75,144 was accrued as of December 31,
2015.
-39-
The
Company paid bonuses to certain employees based on their
performance, the Company’s need to retain such employees, and
funds available. All bonus payments were approved by the
Company’s Board of Directors.
Outstanding Equity Awards at Fiscal Year-End Table
The
following table sets forth all outstanding equity awards held by
the Company’s Named Executive Officers as of the end of last
fiscal year.
|
Option
Awards
|
|||
Name
|
Number of
SecuritiesUnderlyingUnexercised Options(#) Exercisable
|
Number of
SecuritiesUnderlying Unexercised Options (#)
Unexercisable
|
Option
Exercise Price
($)
|
Option
Expiration
Date
|
James C.
Katzaroff
|
32,500
|
-
|
$15.00
|
2/11/23
|
James C.
Katzaroff
|
100,000
|
-
|
$1.00
|
6/21/19
|
James C.
Katzaroff
|
1,000,000
|
-
|
$0.50
|
6/21/21
|
L. Bruce
Jolliff
|
480,000
|
176,548
|
$0.50
|
6/21/21
|
Employment Agreement with Significant Employee
Employment
Agreement with Dr. Fu Min-Su
In
January 2008, the Company entered into a five-year employment
agreement with Dr. Fu Min-Su pursuant to which the Company agreed
to pay Dr. Fu Min-Su an annual salary equal to $90,000, which was
increased to $95,000 on January 1, 2010, to $110,000 on January 1,
2011, and to $125,000 effective June 1, 2016.
In
the event the
employment is terminated by the Company without cause, by Dr. Fu
Min-Su for good reason or a change in control, the Company will
have to provide Dr. Fu Min-Su with one month of his base salary and
any portion of an annual bonus allocated by the Board of Directors,
disability and other welfare plan benefits for a period
of one year from the date of termination and pro-rated vesting of
all outstanding
options, stock grants, shares of restricted stock and any other
equity incentive compensation; provided, that the stock options
shall be exercisable only until the earlier to occur of (i) two
years from the date of the termination, or (ii) the date the option
would have otherwise expired if Dr. Fu Min-Su had not
terminated employment.
During
the term of the employment agreement, including any extension
thereof, and for a period of one year thereafter, Dr. Fu Min-Su
shall not provide services that he provides for the Company for a
business in the production, import for resale, and distribution of
radioisotopes for use in the medical industries.
Compensation of Directors
During
the year ended December 31, 2016, the Company’s non-employee
directors were not paid any compensation.
The
following table sets forth, for each of the Company’s
non-employee directors who served during 2016, the aggregate number
of stock awards and the aggregate number of stock option awards
that were outstanding as of December 31, 2016:
|
Outstanding
|
Outstanding
|
|
Stock
|
Stock
|
Name
|
Awards (#)
|
Options (#)
|
Carlton M.
Cadwell
|
-
|
100,000
|
Thomas J.
Clement
|
-
|
100,000
|
During
June 2016, the Company granted to Messrs. Cadwell and Clement
options to purchase 100,000 shares of common stock at an exercise
price of $1.00 per share. The options are fully vested and expire
June 21, 2019.
There
are no employment contracts or compensatory plans or arrangements
with respect to any director that would result in payments by the
Company to such person because of his or her resignation as a
director or any change in control of the
Company.
-40-
SECURITY OWNERSHIP OF CERTAIN BENEFICIAL OWNERS AND
MANAGEMENT
Beneficial Ownership of the Company’s Common
Stock
The
following table sets forth, as of March 6, 2017, the number of
shares of common stock beneficially owned by the following persons:
(i) all persons the Company knows to be beneficial owners of at
least 5% of the Company’s common stock, (ii) the
Company’s directors, (iii) the Company’s executive
officers, both of whom are named in the Summary Compensation Table
above, and (iv) all current directors and executive officers as a
group.
As of
March 6, 2017, there were 37,541,697 shares outstanding and up
to 11,637,245 shares issuable upon exercise of outstanding options,
warrants, and conversion of outstanding convertible securities,
assuming exercise and conversion occurred as of that date, for a
total of 49,178,942 shares.
Name
and Address of Beneficial Owner(1)
|
Amount and Nature of Beneficial
Ownership(2)
|
Percent of Class
|
Cadwell Family
Irrevocable Trust
|
169,839
|
0.5%
|
|
|
|
Carlton M.
Cadwell(3)
|
1,268,844
|
3.4%
|
|
|
|
James C.
Katzaroff(4)
|
1,409,860
|
3.7%
|
|
|
|
Thomas J.
Clement(3)
|
100,000
|
0.3%
|
|
|
|
L. Bruce
Jolliff(5)
|
635,034
|
1.7%
|
|
|
|
All Current
Directors and Executive Officers as a group (5
individuals)
|
3,583,577
|
7.1%
|
(1)
The
address of each of the beneficial owners above is c/o Advanced
Medical Isotope Corporation, 1021 N. Kellogg Street, Kennewick, WA
99336, except that the address of the Cadwell Family Irrevocable
Trust (the “Cadwell
Trust ”) is 909 North Kellogg Street, Kennewick,
WA 99336.
(2)
In
determining beneficial ownership of the Company’s common
stock as of a given date, the number of shares shown includes
shares of common stock which may be acquired upon exercise of
options or conversion of convertible securities within 60 days of
that date. In determining the percent of common stock owned by a
person or entity on February 1, 2017, (a) the numerator
is the number of shares of the class beneficially owned by such
person or entity, including shares which may be acquired within 60
days on exercise of options and conversion of convertible
securities, and (b) the denominator is the sum of (i) the
total shares of common stock outstanding on February 1, 2017, and
(ii) the total number of shares that the beneficial owner may
acquire upon conversion of the convertible securities and upon
exercise of the options. Subject to community property laws where
applicable, the Company believes that each beneficial owner has
sole power to vote and dispose of its shares, except that Mr.
Cadwell under the terms of the Cadwell Trust does not have or share
voting or investment power over the shares beneficially owned by
the Cadwell Trust.
(3)
Includes 100,000
shares each issuable under options to Mr. Cadwell and Mr.
Clements.
(4)
Includes 1,232,500
shares issuable under options held by Mr. Katzaroff.
(5)
Includes 480,000
shares issuable under options held by Mr. Jolliff.
-41-
Beneficial Ownership of the Company’s Preferred
Stock
The
following table sets forth, as of March 6, 2017, the
number of shares of preferred stock beneficially owned by the
following persons: (i) all persons the Company known to be
beneficial owners of at least 5% of the Company’s preferred
stock, (ii) the Company’s directors, (iii) the
Company’s executive officers, both of whom are named in the
Summary Compensation Table above, and (iv) all current directors
and executive officers as a group.
Name and Address of Beneficial
Owner(1)
|
Amount and Nature of Beneficial
Ownership(2)
|
Percent of Class
|
Cadwell Family
Irrevocable Trust
|
148,309
|
4.5%
|
|
|
|
Carlton M.
Cadwell
|
908,910
|
27.6%
|
|
|
|
James C.
Katzaroff
|
-
|
-%
|
|
|
|
Thomas J.
Clement
|
-
|
-%
|
|
|
|
L. Bruce
Jolliff
|
114,700
|
3.5%
|
|
|
|
All Current
Directors and Executive Officers as a group (5
individuals)
|
1,171,919
|
35.5%
|
(1)
The
address of each of the beneficial owners above is c/o Advanced
Medical Isotope Corporation, 1021 N. Kellogg Street, Kennewick, WA
99336, except that the address of the Cadwell Family Irrevocable
Trust (the “Cadwell
Trust ”) is 909 North Kellogg Street, Kennewick,
WA 99336.
(2)
In
determining beneficial ownership of the Company’s common
stock as of a given date, the number of shares shown includes
shares of common stock which may be acquired upon exercise of
options or conversion of convertible securities within 60 days of
that date. In determining the percent of common stock owned by a
person or entity on February 13, 2017, (a) the numerator
is the number of shares of the class beneficially owned by such
person or entity, including shares which may be acquired within 60
days on exercise of options and conversion of convertible
securities, and (b) the denominator is the sum of (i) the
total shares of common stock outstanding on February 13, 2017, and
(ii) the total number of shares that the beneficial owner may
acquire upon conversion of the convertible securities and upon
exercise of the options. Subject to community property laws where
applicable, the Company believes that each beneficial owner has
sole power to vote and dispose of its shares, except that Mr.
Cadwell under the terms of the Cadwell Trust does not have or share
voting or investment power over the shares beneficially owned by
the Cadwell Trust.
Changes in Control
The
Company does not know of any arrangements, including any pledges of
the Company’s securities that may result in a change in
control of the Company.
-42-
CERTAIN RELATIONSHIPS AND RELATED PARTY TRANSACTIONS
On
occasion we may engage in certain related party transactions. All
prior related party transactions were approved by a majority of the
disinterested directors. Upon the consummation of offering, our
policy is that all related party transactions will be reviewed and
approved by the independent members of our board of directors prior
to our entering into any related party transactions.
Indebtedness from Related Parties
Beginning in
December, 2008, the Company has obtained financing from Carlton M.
Cadwell, one of our directors and a beneficial owner of more than
10% of the Company’s common stock, in transactions which
involved the Company’s issuance of convertible notes and
common stock. On September 4, 2015, the Company exchanged
$1,414,100 of convertible notes plus $810,538 of accrued interest
into 148,311 shares of Series A Preferred and another $2,224,466 of
convertible notes plus $889,838 of accrued interest into 207,620
shares of Series A Preferred. Additionally, the Company exchanged
the remaining $906,572 of convertible notes plus $148,960 accrued
interest into a $1,055,532 demand note, 8% interest rate, due on
demand at any time after March 31, 2017. Such note was converted
into 73,546 shares of Series A Preferred on May 19, 2016.
At December 31, 2016 Mr. Cadwell has
an aggragate total of $332,195 in promissory
notes.
Independent Directors
The
Company’s common stock is traded on the OTC Pink Marketplace,
which does not impose any independence requirements on the board of
directors or the board committees of the companies whose stock is
traded on that market. The Company has decided to adopt
the independence standards of the NASDAQ listing rules in
determining whether the Company’s directors are
independent. Generally, under those rules a director
does not qualify as an independent director if the director or a
member of the director’s immediate family has had in the past
three years certain relationships or affiliations with the Company,
the Company’s auditors, or other companies that do business
with the Company. The Company’s board of directors
has determined that Mr. Cadwell and Mr. Clement each qualified as
an independent director under those NASDAQ rules, and accordingly,
each would have been qualified under those rules to serve on a
compensation committee or a nominating committee, if the Company
had established such committees of the Company’s Board of
Directors. Mr. Katzaroff is not an independent director due to his
employment by the Company as an executive officer.
-43-
DESCRIPTION OF SECURITIES
Authorized
Capital Stock
Our
authorized capital stock consists of 2,020,000,000 shares in two
classes designated, respectively, “Common Stock” and
“Preferred Stock.” The total number of shares of Common
Stock authorized to be issued is 2,000,000,000 shares, $0.001 par
value per share. The total number of shares of Preferred Stock
authorized to be issued is 20,000,000 shares, $0.001 par value per
share.
Common Stock
Our
Certificate of Amendment of
Certificate of Incorporation authorizes the issuance of authorized capital of 2,000,000,000 shares of
Common Stock, $0.001 par value per share, of which
37,541,697 were outstanding as of March 7, 2017. Upon
sale, conversion or exercise of
the
shares offered herein, we may have outstanding, up
to
shares of common stock. Holders of shares of common
stock are entitled to one vote for each share on all matters to be
voted on by the stockholders. Holders of common stock have no
cumulative voting rights, but are entitled to one vote for each
shares of common stock they hold. Holders of shares of common stock
are entitled to share ratably in dividends, if any, as may be
declared, from time to time by the board of directors in its
discretion, from funds legally available to be distributed. In the
event of a liquidation, dissolution or winding up of the Company,
the holders of shares of common stock are entitled to share pro
rata all assets remaining after payment in full of all liabilities
and the prior payment to the preferred stockholders if any. Holders
of common stock have no preemptive rights to purchase our common
stock. There are no conversion rights or redemption or sinking fund
provisions with respect to the common stock.
Preferred Stock
The Company’s Board of Directors (the
“Board”) is currently authorized, without further
shareholder approval, to issue from time to time up to an aggregate
of 20.0 million shares of Preferred Stock in one or more series and
to fix or alter the designations, preferences, rights,
qualifications, limitations or restrictions of the shares of each
series, including the dividend rights, dividend rates, conversion
rights, voting rights, term of redemption including sinking fund
provisions, redemption price or prices, liquidation preferences and
the number of shares constituting any series or designations of
such series without further vote or action by the shareholders. The
issuance of Preferred Stock may have the effect of delaying,
deferring or preventing a change in control of management without
further action by the shareholders and may adversely affect the
voting and other rights of the holders of Common Stock. The
issuance of Preferred Stock with voting and conversion rights may
adversely affect the voting power of the holders of Common Stock,
including the loss of voting control to
others.
We currently have one
series of Preferred Stock authorized, the Series A Preferred. The
following is a summary of the rights and preferences of the Series
A Preferred, which summary is not meant to be a complete
descriptions of those terms. For a complete description of the
rights and preferences attributable to the Series A Preferred,
please see the Certificate of Designations, Preferences and Rights
of the Series A Convertible Preferred Stock (the
“Series
A Certificate of Designation”), attached as
Exhibit 4.1 to our Current Report on Form 8-K filed with the
Securities and Exchange Commission (the "SEC")
on July 8, 2015.
Series A Convertible Preferred Stock
In June 2015, the Series A Certificate of
Designation was filed with the Delaware Secretary of State to
designate 2.5 million
shares of our Preferred Stock as Series A
Preferred. Effective March 31, 2016, the Company amended the
Certificate of Designations, Preferences and Rights of Series A
Convertible Preferred Stock of the Registrant, increasing the
maximum number of shares of Series A Preferred Stock from 2,500,000
shares to 5,000,000 shares. The following summarizes the current
rights and preferences of the Series A
Preferred:
Liquidation
Preference. The Series A
Preferred has a liquidation preference of $5.00 per
share.
Conversion. Subject
to certain limitations set forth in the Series A Certificate of
Designation, each share of Series A Preferred is convertible, at
the option of the holder, into that number of shares of Common
Stock (the “Series
A Conversion Shares”) equal to the
liquidation preference thereof, divided by Conversion Price (as
such term is defined in the Series A Certificate of Designation),
currently $0.50.
-44-
In the event the Company completes an equity or equity-based public
offering, registered with the SEC, resulting in gross proceeds to
the Company totaling at least $5.0 million, all issued and
outstanding shares of Series A Preferred at that time will
automatically convert into Series A Conversion Shares.
Voting Rights.
Holders of Series A Preferred are entitled to vote on all matters,
together with the holders of Common Stock, and have the equivalent
of five (5) votes for every Series A Conversion Share issuable upon
conversion of such holder’s outstanding shares of Series A
Preferred. However, the Series A Conversion
Shares, when issued, will have all of the same voting rights as
other issued and outstanding Common Stock of the Company, and none
of the rights of the Series A Preferred.
Liquidation.
Upon any liquidation, dissolution, or winding-up of the
Company, whether voluntary or involuntary (a
“Liquidation”), the holders of Series A Preferred shall
be entitled to receive out of the assets, whether capital or
surplus, of the Company an amount equal to the liquidation
preference of the Series A Preferred before any distribution or
payment shall be made to the holders of any junior securities, and
if the assets of the Company is insufficient to pay in full such
amounts, then the entire assets to be distributed to the holders of
the Series A Preferred shall be ratably distributed among the
holders in accordance with the respective amounts that would be
payable on such shares if all amounts payable thereon were paid in
full.
Certain Price and
Share Adjustments.
a) Stock
Dividends and Stock Splits. If the Company (i) pays a stock dividend
or otherwise makes a distribution or distributions payable in
shares of Common Stock on shares of Common Stock or any other
Common Stock equivalents; (ii) subdivides outstanding shares of
Common Stock into a larger number of shares; (iii) combines
(including by way of a reverse stock split) outstanding shares of
Common Stock into a smaller number of shares; or (iv) issues, in
the event of a reclassification of shares of the Common Stock, any
shares of capital stock of the Company, then the conversion price
shall be adjusted accordingly.
b) Merger
or Reorganization. If the
Company is involved in any reorganization, recapitalization,
reclassification, consolidation or merger in which the Common Stock
is converted into or exchanged for securities, cash or other
property than each share of Series A Preferred shall be
convertible into the kind and amount of securities, cash or other
property that a holder of the number of shares of Common Stock
issuable upon conversion of one share of Series A Preferred
prior to any such merger or reorganization would have been entitled
to receive pursuant to such transaction.
Options
As of March 7,
2017, we had options to purchase 2,402,500 shares of our common
stock outstanding, with a weighted exercise price of $0.81 per
share.
Warrants
As of March 7,
2017, warrants to purchase 3,579,505 shares of our common stock
were outstanding, with a weighted average exercise price of $4.45
per share.
-45-
Warrants Offered Hereby
We
are offering warrants to purchase up to
shares of our common stock to purchasers in this
offering. Each warrant entitles the holder thereof to
purchase one share of common stock at an exercise price of $ per
share ( of the public offering price of our
common stock).
The
following is a brief summary of certain terms and conditions of the
warrants to be issued in connection with this offering and are
subject in all respects to the provisions contained in the
warrants.
Form
The warrants will be issued in electronic
book-entry form to participants in this offering.
You should review a copy of the form
of warrant, which is filed as an exhibit to the registration
statement of which this prospectus forms a part, for a complete
description of the terms and conditions applicable to the
warrants.
Exercisability
The warrants are exercisable at any time after
their original issuance, expected to be, 2017, and at any time up
to the date that is
years after
their original issuance. The warrants will be exercisable, at the
option of each holder, in whole or in part by delivering to us a
duly executed exercise notice and, at any time a registration
statement registering the issuance of the shares of common stock
underlying the warrants under the Securities Act is effective and
available for the issuance of such shares, or an exemption from
registration under the Securities Act is available for the issuance
of such shares, by payment in full in immediately available funds
for the number of shares of common stock purchased upon such
exercise. If a registration statement registering the issuance of
the shares of common stock underlying the warrants under the
Securities Act is not effective or available andan exemption from
registration under the Securities Act is not available for the
issuance of such shares, the holder may, in its sole discretion,
elect to exercise the warrant through a cashless exercise, in which
case the holder would receive upon such exercise the net number of
shares of common stock determined according to the formula set
forth in the warrant. No fractional shares of common stock will be
issued in connection with the exercise of a warrant. In lieu of
fractional shares, we will pay the holder an amount in cash equal
to the fractional amount multiplied by the exercise
price.
Exercise Limitation
A
holder will not have the right to exercise any portion of the
warrant if the holder (together with its affiliates) would
beneficially own in excess of 4.99% of the number of shares of our
common stock outstanding immediately after giving effect to the
exercise, as such percentage ownership is determined in accordance
with the terms of the warrants. However, any holder may increase or
decrease such percentage to any other percentage not in excess of
9.99% upon at least 61 days’ prior notice from the holder to
us.
Exercise Price
The exercise price per whole share of common stock
purchasable upon exercise of the warrants is $ per share of common
stock, which represents of the public offering
price of the shares of common stock in this offering. The exercise price is subject to appropriate
adjustment in the event of certain stock dividends and
distributions, stock splits, stock combinations, reclassifications
or similar events affecting our common stock and also upon any
distributions of assets, including cash, stock or other property to
our stockholders.
-46-
Transferability
Subject
to applicable laws, the warrants may be offered for sale, sold,
transferred or assigned without our consent.
Exchange Listing
There
is no established public trading market for the warrants and we do
not intend to apply to list the warrants on any securities exchange
or automated quotation system.
Rights as a Stockholder
Except
as otherwise provided in the warrants or by virtue of such
holder’s ownership of shares of our common stock, the holder
of a warrant does not have the rights or privileges of a holder of
our common stock, including any voting rights, until the holder
exercises the warrant.
Delaware Laws
The
Delaware Business Corporation Law contains a provision governing
“Acquisition of Controlling
Interest.” This law provides generally that any person
or entity that acquires 20% or more of the outstanding voting
shares of a publicly-held Delaware corporation in the secondary
public or private market may be denied voting rights with respect
to the acquired shares, unless a majority of the disinterested
stockholders of the corporation elects to restore such voting
rights in whole or in part. The control share acquisition act
provides that a person or entity acquires “control
shares” whenever it acquires shares that, but for the
operation of the control share acquisition act, would bring its
voting power within any of the following three ranges:
●
20% to 33%
●
33% to 50%
●
more than 50%
A
“control share acquisition” is generally defined as the
direct or indirect acquisition of either ownership or voting power
associated with issued and outstanding control shares. The
stockholders or board of directors of a corporation may elect to
exempt the stock of the corporation from the provisions of the
control share acquisition act through adoption of a provision to
that effect in the articles of incorporation or bylaws of the
corporation. Our articles of incorporation and bylaws do exempt our
common stock from the control share acquisition act.
-47-
SHARES ELIGIBLE FOR FUTURE SALE
Future
sales of substantial amounts of common stock in the public market
could adversely affect market prices prevailing from time to time.
Furthermore, since only a limited number of shares will be
available for sale shortly after this offering because of certain
restrictions on resale, sales of substantial amounts of our common
stock in the public market after the restrictions lapse could
adversely affect the prevailing market price and our ability to
raise equity capital in the future.
Upon
completion of this offering, and assuming the exercise or
conversion of all derivative securities, we may have outstanding an
aggregate of up to issued and outstanding. Of these shares,
at least will be freely tradable without restriction or further
registration under the Securities Act, unless such shares are
purchased by individuals who become “affiliates” as
that term is defined in Rule 144 under the Securities Act, as the
result of the securities they acquire in this offering which
provide them, directly or indirectly, with control or the capacity
to control us. Our officers and directors will not be purchasing
shares in this offering. The remaining shares of common stock held
by our existing stockholders are “restricted
securities” as that term is defined in Rule 144 under the
Securities Act. Restricted shares may be sold in the public market
only if registered or if they qualify for an exemption from
registration under Rule 144 and or Section 4(a)(1). As a result of
these provisions of Rules 144, additional shares will be available
for sale in the public market as follows:
●
no
restricted shares will be eligible for immediate sale on the date
of this prospectus; and
●
the
remainder of the restricted shares will be eligible for sale from
time to time pursuant to available exemptions, subject to
restrictions on such sales by affiliates.
Sales
pursuant to Rule 144 are subject to certain requirements relating
to the availability of current public information about us. A
person (or persons whose shares are aggregated) who is not deemed
to have been an affiliate of the Company at any time during the 90
days immediately preceding the sale and who has beneficially owned
restricted shares for at least six months is entitled to sell such
shares under Rule 144 without regard to the resale
limitations.
The SEC
has adopted rules that regulate broker-dealer practices in
connection with transactions in “penny stocks.” Penny
stocks generally are equity securities with a price of less than
$5.00, other than securities registered on certain national
securities exchanges or quoted on the Nasdaq system, provided that
current price and volume information with respect to transactions
in such securities is provided by the exchange or system. The penny
stock rules require a broker-dealer, prior to a transaction in a
penny stock not otherwise exempt from the rules, to deliver to the
prospective purchaser a standardized risk disclosure document
prepared by the SEC that provides information about penny stocks
and the nature and level of risks in the penny stock market. In
addition, the penny stock rules require that prior to a transaction
in a penny stock not otherwise exempt from such rules; the
broker-dealer must make a special written determination that the
penny stock is a suitable investment for the prospective purchaser
and receive the purchaser’s written agreement to the
transaction. Furthermore, subsequent to a transaction in a penny
stock, the broker-dealer will be required to deliver monthly or
quarterly statements containing specific information about the
penny stock. It is anticipated that our common stock will be traded
on an OTC market at a price of less than $5.00. In this event,
broker-dealers would be required to comply with the disclosure
requirements mandated by the penny stock rules.
These
disclosure requirements will likely make it more difficult for
investors in this offering to sell their common stock in the
secondary market.
-48-
PLAN OF DISTRIBUTION
We
may sell the securities described in this prospectus to or through
underwriters or dealers, through agents, or directly to one or more
purchasers. A pre-effective amendment to the registration
statement, of which this prospectus forms a part (and any related
prospectus supplement and/or free writing prospectus that we may
authorize to be provided to you) will describe the terms of the
offering of the securities, including, to the extent
applicable:
●
the
name or names of any underwriters, if applicable;
●
the
purchase price of the securities and the proceeds we will receive
from the sale;
●
any
over-allotment options under which underwriters may purchase
additional securities from us;
●
any
agency fees or underwriting discounts and other items constituting
agents’ or underwriters’ compensation;
●
any
public offering price;
●
any
discounts or concessions allowed or reallowed or paid to dealers;
and
●
any
securities exchange or market on which the securities may be
listed.
Only
underwriters named in the registration statement, of which this
prospectus forms a part, are underwriters of the securities offered
by the prospectus.
If
underwriters are used in the sale, they will acquire the securities
for their own account and may resell the securities from time to
time in one or more transactions at a fixed public offering price
or at varying prices determined at the time of sale. The
obligations of the underwriters to purchase the securities will be
subject to the conditions set forth in the applicable underwriting
agreement. We may offer the securities to the public through
underwriting syndicates represented by managing underwriters or by
underwriters without a syndicate. Subject to certain conditions,
the underwriters will be obligated to purchase all of the
securities offered by the prospectus contained in this registration
statement. Any public offering price and any discounts or
concessions allowed or reallowed or paid to dealers may change from
time to time. We may use underwriters with whom we have a material
relationship. We will describe in a pre-effective amendment to the
registration statement, of which this prospectus forms a part, the
nature of any such relationship.
We
may sell securities directly or through agents we designate from
time to time. We will name any agent involved in the offering and
sale of securities, and we will describe any commissions we will
pay the agent in a pre-effective amendment to the registration
statement, of which this prospectus forms a part. Unless the
prospectus contained in this registration statement states
otherwise, our agent will act on a best-efforts basis for the
period of its appointment.
We may provide agents and underwriters with
indemnification against civil liabilities related to this offering,
including liabilities under the Securities Act of 1933, as amended
(the "Securities
Act"), or contribution with
respect to payments that the agents or underwriters may make with
respect to these liabilities. Agents and underwriters may engage in
transactions with, or perform services for, us in the ordinary
course of business.
Any
underwriter may engage in overallotment, stabilizing transactions,
short covering transactions and penalty bids in accordance with
Regulation M under the Exchange Act. Overallotment involves sales
in excess of the offering size, which create a short position.
Stabilizing transactions permit bids to purchase the underlying
security so long as the stabilizing bids do not exceed a specified
maximum. Short covering transactions involve purchases of the
securities in the open market after the distribution is completed
to cover short positions. Penalty bids permit the underwriters to
reclaim a selling concession from a dealer when the securities
originally sold by the dealer are purchased in a covering
transaction to cover short positions. Those activities may cause
the price of the securities to be higher than it would otherwise
be. If commenced, the underwriters may discontinue any of the
activities at any time.
Any
underwriters who are qualified market makers on the NASDAQ Capital
Market may engage in passive market making transactions in
accordance with Rule 103 of Regulation M during the business day
prior to the pricing of the offering, before the commencement of
offers or sales of the securities. Passive market makers must
comply with applicable volume and price limitations and must be
identified as passive market makers. In general, a passive market
maker must display its bid at a price not in excess of the highest
independent bid for such security; if all independent bids are
lowered below the passive market maker’s bid, however, the
passive market maker’s bid must then be lowered when certain
purchase limits are exceeded.
-49-
CHANGES IN AND DISAGREEMENTS WITH ACCOUNTANTS
ON ACCOUNTING ISSUES AND FINANCIAL DISCLOSURE
On,
August 18, 2016, Haynie & Company, Salt Lake City, Utah,
resigned as the Company’s independent registered public
accounting firm. On September 1, 2016, (the "Resignation Date") the Company engaged
Fruci & Associates II, PLLC (“Fruci”), as its new independent
registered public accounting firm. The change of the
Company’s independent registered public accounting firm from
Haynie & Company to Fruci was approved unanimously by our Board
of Directors.
The
report of Haynie & Company on the Company’s financial
statements for the fiscal year ended December 31, 2015 did not
contain an adverse or disclaimer of opinion and were not qualified
or modified as to uncertainty, audit scope, or accounting
principles, except the report did contain an explanatory paragraph
related to the Company’s ability to continue as a going
concern.
During
the two most recent fiscal years and through the Resignation Date,
there were (i) no disagreements between the Company and Haynie
& Company or Fruci on any matter of accounting principles or
practices, financial statement disclosure, or auditing scope or
procedures, which disagreement, if not resolved to the satisfaction
of Haynie & Company and Fruci, would have caused Haynie &
Company or Fruci to make reference thereto in their reports on the
consolidated financial statements for such years, and (ii) with the
exception of material weaknesses related to our internal control
over financial reporting, no “reportable events” as
that term is defined in Item 304(a)(1)(v) of Regulation
S-K.
LEGAL MATTERS
________________
has issued an opinion that the shares being issued pursuant to this
offering, upon issuance, are duly authorized and validly issued,
fully paid and non-assessable.
EXPERTS
The
consolidated balance sheet of Advanced Medical Isotope Corporation
as of December 31, 2015 and the related consolidated statements of
operations, stockholders’ equity (deficit), and cash flows
for the year then ended, have been audited by Haynie & Company, an independent
registered public accounting firm, as stated in their report which
is included herein, which report includes an emphasis of matter
paragraph about the Company’s ability to continue as a going
concern. Such financial statements have been so included herein in
reliance on the report of said firm given upon their authority as
experts in accounting and auditing.
The
consolidated balance sheet of Advanced Medical Isotope Corporation
as of December 31, 2016 and the related consolidated statements of
operations, stockholders’ equity (deficit), and cash flows
for the year then ended, have been audited by Fruci & Associates II, PLLC, an
independent registered public accounting firm, as stated in their
report which is included herein, which report includes an emphasis
of matter paragraph about the Company’s ability to continue
as a going concern. Such financial statements have been so included
herein in reliance on the report of said firm given upon their
authority as experts in accounting and auditing.
No
expert or counsel named in this prospectus as having prepared or
certified any part of this prospectus or having given an opinion
upon the validity of the securities being registered or upon other
legal matters in connection with the registration or offering of
the common stock was employed for such purpose on a contingency
basis, or had, or is to receive, in connection with this offering,
a substantial interest, direct or indirect, in us or any of our
subsidiaries, nor was any such person connected with us as a
promoter, managing or principal underwriter, voting trustee,
director, officer, or employee.
-50-
WHERE YOU CAN FIND MORE INFORMATION
We have filed a registration statement on Form S-1
with the SEC. This prospectus, which forms a part of that
registration statement, does not contain all of the information
included in the registration statement and the exhibits and
schedules thereto as permitted by the rules and regulations of the
SEC. For further information with respect to us and the shares of
our common stock offered hereby, please refer to the registration
statement, including its exhibits and schedules. Statements
contained in this prospectus as to the contents of any contract or
other document referred to herein are not necessarily complete and,
where the contract or other document is an exhibit to the
registration statement, each such statement is qualified in all
respects by the provisions of such exhibit, to which reference is
hereby made. You may review a copy of the registration statement at
the SEC’s public reference room at 100 F Street, N.E.,
Washington, DC 20549. Please call the SEC at 1-800-SEC-0330 for
further information on the operation of the public reference rooms.
The registration statement can also be reviewed by accessing the
SEC’s website at http://www.sec.gov.
We are subject to the information and reporting requirements of the
Exchange Act and, in accordance therewith, file periodic reports,
proxy statements or information statements, and other information
with the SEC. These reports can also be reviewed by accessing the
SEC’s website.
You should rely only on the information
provided in this prospectus, any prospectus supplement or as part
of the registration statement filed on Form S-1 of which this
prospective is a part, as such registration statement is amended
and in effect with the Securities and Exchange Commission. We have
not authorized anyone else to provide you with different
information. We are not making an offer of these securities in any
state where the offer is not permitted. You should not assume that
the information in this prospectus, any prospectus supplement or
any document incorporated by reference is accurate as of any date
other than the date of those documents.
-51-
Advanced Medical Isotope Corporation
Index to Financial Statements
|
|
Pages
|
|
|
|
Report
of Independent Registered Public Accounting Firm for
2016
|
|
F-1
|
|
|
|
Report
of Independent Registered Public Accounting Firm for
2015
|
|
F-2
|
|
|
|
Financial Statements:
|
|
|
|
|
|
Consolidated
Balance Sheets as of December 31, 2016 and 2015
|
|
F-3
|
|
|
|
Consolidated
Statements of Operations for the years ended December 31, 2016 and
2015
|
|
F-4
|
|
|
|
Consolidated
Statement of Changes in Stockholders’ Equity (Deficit) for
the years ended December 31, 2016 and 2015
|
|
F-5
|
|
|
|
Consolidated
Statements of Cash Flow for the years ended December 31, 2016
and 2015
|
|
F-6
|
|
|
|
Notes
to Consolidated Financial Statements
|
|
F-7
|
-52-
|
Report
of Independent Registered Public Accounting Firm
To the
Board of Directors and
Stockholders
of Advanced Medical Isotope Corporation
We have
audited the accompanying consolidated balance sheet of Advanced
Medical Isotope Corporation as of December 31, 2016, and the
related consolidated statement of operations, stockholders’
equity (deficit), and cash flows for the year ended December 31,
2016. Advanced Medical Isotope Corporation’s management is
responsible for these consolidated financial statements. Our
responsibility is to express an opinion on these financial
statements based on our audit.
We
conducted our audit in accordance with the standards of the Public
Company Accounting Oversight Board (United States). Those standards
require that we plan and perform the audit to obtain reasonable
assurance about whether the consolidated financial statements are
free of material misstatement. The company is not required to have,
nor were we engaged to perform, an audit of its internal control
over financial reporting. Our audit included consideration of
internal control over financial reporting as a basis for designing
audit procedures that are appropriate in the circumstances, but not
for the purpose of expressing an opinion on the effectiveness of
the company’s internal control over financial reporting.
Accordingly, we express no such opinion. An audit also includes
examining, on a test basis, evidence supporting the amounts and
disclosures in the financial statements, assessing the accounting
principles used and significant estimates made by management, as
well as evaluating the overall financial statement presentation. We
believe that our audit provides a reasonable basis for our
opinion.
In our
opinion, the consolidated financial statements referred to above
present fairly, in all material respects, the financial position of
Advanced Medical Isotope Corporation as of December 31, 2016, and
the results of its operations and its cash flows for the year ended
December 31, 2016, in conformity with accounting principles
generally accepted in the United States of America.
The
accompanying consolidated financial statements have been prepared
assuming the Company will continue as a going concern. As discussed
in Note 1 to the consolidated financial statements, the Company has
a history of recurring losses, has limited cash, resources, and,
based upon current operating levels, its viability is dependent
upon its ability to meet future financing requirements or
restructuring to sustain its operations. These issues raise
substantial doubt about the Company’s ability to continue as
a going concern. Management’s plans in regard to these
matters are also described in Note 1. The consolidated financial
statements do not include any adjustments that might result from
the outcome of this uncertainty.
/s/ Fruci & Associates II,
PLLC
Fruci
& Associates II, PLLCSpokane, WA
March 8,
2017
F-1
Report
of Independent Registered Public Accounting Firm
To the Board of
Directors and Shareholders
Advanced Medical
Isotope Corporation
We have audited the
accompanying balance sheet of Advanced Medical Isotope Corporation
as of December 31, 2015, and the related statements of operations,
stockholders’ equity (deficit), and cash flow for the year
then ended. These financial statements are the responsibility of
the Company’s management. Our responsibility is to express an
opinion on these financial statements based on our
audit.
We conducted our
audit in accordance with the standards of the Public Company
Accounting Oversight Board (United States). Those standards require
that we plan and perform the audit to obtain reasonable assurance
about whether the financial statements are free of material
misstatement. The Company is not required to have, nor were we
engaged to perform, an audit of its internal control over financial
reporting. Our audit included consideration of internal control
over financial reporting as a basis for designing audit procedures
that are appropriate in the circumstances, but not for the purpose
of expressing an opinion on the effectiveness of the
Company’s internal control over financial reporting.
Accordingly, we express no such opinion. An audit also includes
examining, on a test basis, evidence supporting the amounts and
disclosures in the financial statements, assessing the accounting
principles used and significant estimates made by management, as
well as evaluating the overall financial statement presentation. We
believe that our audit provides a reasonable basis for our
opinion.
In our opinion, the
financial statements referred to above present fairly, in all
material respects, the financial position of Advanced Medical
Isotope Corporation as of December 31, 2015, and the results of its
operations and its cash flows for the year then ended, in
conformity with U.S. generally accepted accounting
principles.
The accompanying
financial statements have been prepared assuming that the Company
will continue as a going concern. As discussed in Note 1 to the
financial statements, the Company has suffered recurring losses,
used significant cash in support of its operating activities, and,
based upon current operating levels, requires additional capital or
significant restructuring to sustain its operations for the
foreseeable future. These issues raise substantial doubt about the
Company’s ability to continue as a going concern.
Management’s plans in regard to these matters are also
described in Note 1. The financial statements do not include any
adjustments that might result from the outcome of this
uncertainty.
Haynie &
Company
Salt Lake City,
Utah
May 25,
2016
F-2
Advanced
Medical Isotope Corporation
Consolidated
Balance Sheets
|
December
31,
|
|
|
2016
|
2015
|
ASSETS
|
|
|
|
|
|
Current
assets:
|
|
|
Cash
|
$27,889
|
$179,032
|
Prepaid
expenses
|
11,990
|
26,211
|
Inventory
|
-
|
8,475
|
Total current
assets
|
39,879
|
213,718
|
|
|
|
Fixed assets, net
of accumulated depreciation
|
1,473
|
4,420
|
|
|
|
Other
assets:
|
|
|
Patents and
intellectual property
|
-
|
35,482
|
Deposits
|
644
|
644
|
Total other
assets
|
644
|
36,126
|
|
|
|
Total
assets
|
$41,996
|
$254,264
|
|
|
|
LIABILITIES
AND STOCKHOLDERS’ EQUITY (DEFICIT)
|
|
|
|
|
|
Current
liabilities:
|
|
|
Accounts payable
and accrued expenses
|
$1,137,086
|
$1,182,112
|
Related party
accounts payable
|
109,718
|
102,647
|
Accrued interest
payable
|
114,755
|
229,246
|
Payroll liabilities
payable
|
499,502
|
298,900
|
Convertible notes
payable, net
|
544,508
|
1,788,384
|
Derivative
liability
|
324,532
|
4,235,016
|
Related party
promissory note
|
332,195
|
1,280,450
|
Liability for lack
of authorized shares
|
-
|
852,091
|
Total current
liabilities
|
3,062,296
|
9,968,846
|
|
|
|
Total
liabilities
|
3,062,296
|
9,968,846
|
|
|
|
Commitments
and contingencies
|
|
|
|
|
|
MEZZANINE
EQUITY
|
|
|
Preferred stock,
$.001 par value, 20,000,000 shares of authorized preferred stock,
$.001 par value, 5,000,000 Series A shares
authorized; 3,773,592 and 1,627,000 - shares issued and
outstanding, respectively
|
14,144,571
|
4,617,052
|
Total mezzanine
equity
|
14,144,571
|
4,617,052
|
Stockholders’
equity (deficit):
|
|
|
Common stock, $.001
par value; 2,000,000,000 shares authorized; 31,743,797 and
19,969,341 shares issued and outstanding,
respectively
|
31,744
|
19,969
|
Paid in
capital
|
40,672,825
|
33,662,942
|
Accumulated
deficit
|
(57,869,440)
|
(48,014,545)
|
Total
stockholders’ equity (deficit)
|
(17,164,871)
|
(14,331,634)
|
|
|
|
Total liabilities
and stockholders’ equity (deficit)
|
$41,996
|
$254,264
|
The accompanying
notes are an integral part of these consolidated financial
statements.
F-3
Advanced
Medical Isotope Corporation
Consolidated
Statements of Operations
|
Year
ended
|
|
|
December
31,
|
|
|
2016
|
2015
|
Consulting
revenues
|
$8,108
|
$24,108
|
|
|
|
Operating
expenses
|
|
|
Cost of
materials
|
-
|
474
|
Sales and marketing
expenses
|
284,138
|
-
|
Depreciation and
amortization expense
|
2,947
|
5,672
|
Professional
fees
|
2,068,796
|
741,375
|
Stock based
compensation
|
675,324
|
80,635
|
Payroll
expenses
|
652,877
|
679,259
|
Research and
development
|
328,026
|
149,650
|
General and
administrative expenses
|
432,470
|
408,306
|
Total operating
expenses
|
4,444,578
|
2,065,371
|
|
|
|
Operating
loss
|
(4,436,470)
|
(2,041,263)
|
|
|
|
Non-operating
income (expense):
|
|
|
Interest
expense
|
(6,259,467)
|
(3,196,153)
|
Gain on settlement
of debt
|
3,108,342
|
3,562,067
|
Grant
income
|
21,010
|
21,010
|
Gain (loss) on
derivative liability
|
(2,244,353)
|
7,887,025
|
Loss on impaired
assets
|
(43,957)
|
-
|
|
|
|
Non-operating
income (expense), net
|
(5,418,425)
|
8,273,949
|
|
|
|
Income (loss)
before income taxes
|
(9,854,895)
|
6,232,686
|
|
|
|
Income tax
provision
|
-
|
-
|
|
|
|
Net income
(loss)
|
$(9,854,895)
|
$6,232,686
|
|
|
|
Earnings (loss) per
common share
|
$(0.46)
|
$0.34
|
|
|
|
Weighted average
number of common shares outstanding
|
21,497,069
|
18,505,467
|
The accompanying
notes are an integral part of these consolidated financial
statements.
F-4
Advanced Medical Isotope
Corporation
Consolidated
Statements of Changes in Stockholders’ Equity
(Deficit)
|
Common
Stock
|
Paid
in
|
Accumulated
|
|
|
|
Shares
|
Amount
|
Capital
|
Deficit
|
Total
|
Balances
at December 31, 2014
|
17,053,825
|
17,054
|
34,068,009
|
(54,247,231)
|
(20,162,168)
|
|
|
|
|
|
|
Common stock issued
for:
|
|
|
|
|
|
Exercise
of options and warrants
|
1,995,000
|
1,995
|
(1,995)
|
-
|
-
|
Loan fees on
convertible debt
|
43,326
|
43
|
6,344
|
-
|
6,387
|
Conversion of
debt
|
920,516
|
920
|
108,892
|
-
|
109,812
|
Classified to
liability due to lack of authorized shares
|
(43,326)
|
(43)
|
(598,943)
|
-
|
(598,986)
|
Options issued for
services
|
-
|
-
|
80,635
|
-
|
80,635
|
Net
income
|
-
|
-
|
-
|
6,232,686
|
6,232,686
|
|
|
|
|
|
|
Balances
at December 31, 2015
|
19,969,341
|
$19,969
|
$33,662,942
|
$(48,014,545)
|
$(14,331,634)
|
|
|
|
|
|
|
Common stock issued
for:
|
|
|
|
|
|
Exercise
of options and warrants
|
30,644
|
31
|
(31)
|
-
|
-
|
Settlement of
debt
|
563,523
|
564
|
70,299
|
-
|
70,863
|
Conversion of
preferred stock
|
11,180,289
|
11,180
|
4817024
|
-
|
4,828,204
|
Classified to
liability due to lack of authorized shares
|
-
|
-
|
852,092
|
-
|
852,092
|
Options and
warrants issued for services
|
-
|
-
|
1,270,499
|
-
|
1,270,499
|
Net
loss
|
-
|
-
|
-
|
(9,854,895)
|
(9,854,895)
|
|
|
|
|
|
|
Balances
at December 31, 2016
|
31,743,797
|
31,744
|
40,672,825
|
(57,869,440)
|
(17,164,871)
|
The accompanying
notes are an integral part of these consolidated financial
statements.
F-5
Advanced
Medical Isotope Corporation
Consolidated
Statements of Cash Flows
|
Year ended December
31,
|
|
|
2016
|
2015
|
CASH
FLOW FROM OPERATING ACTIVITIES:
|
|
|
Net income
(loss)
|
$(9,854,895)
|
$6,232,686
|
Adjustments to
reconcile net income (loss) to net cash used by operating
activities:
|
|
|
Depreciation of
fixed assets
|
2,947
|
4,333
|
Amortization of
licenses and intangible assets
|
-
|
1,339
|
Amortization of
convertible debt discount
|
604,042
|
1,080,771
|
Amortization of
prepaid expenses paid with stock
|
(2,500)
|
-
|
Amortization of
debt issuance costs
|
-
|
13,917
|
(Gain) loss on
derivative liability
|
2,244,353
|
(7,887,025)
|
(Gain) on
settlement of debt
|
(3,562,067)
|
(3,562,067)
|
Loss on impaired
assets
|
43,957
|
-
|
Preferred stock
issued for services
|
1,003,814
|
334,880
|
Preferred stock
issued for loan fees
|
162,456
|
527,325
|
Stock options and
warrants issued for services
|
1,270,499
|
80,635
|
New derivatives
recorded as loan fees
|
4,935,638
|
-
|
Penalties on notes
payable
|
-
|
1,148,997
|
Changes in
operating assets and liabilities:
|
|
|
Prepaid
expenses
|
16,721
|
(4,501)
|
Accounts
payable
|
102,954
|
151,607
|
Payroll
liabilities
|
200,602
|
252,240
|
Accrued
interest
|
451,041
|
431,758
|
|
|
|
Net cash used by
operating activities
|
(1,926,713)
|
(1,193,105)
|
|
|
|
CASH
FLOWS FROM INVESTING ACTIVITIES
|
-
|
-
|
|
|
|
CASH
FLOWS FROM FINANCING ACTIVITIES:
|
|
|
Principal payments
on capital lease
|
-
|
(39,481)
|
Proceeds from
convertible note
|
1,273,534
|
1,666,415
|
Proceeds from
related party notes
|
723,308
|
-
|
Proceeds from
shareholder advances
|
132,533
|
-
|
Proceeds from
warrant exercised for preferred stock
|
250
|
-
|
Proceeds from sale
of preferred stock
|
70,000
|
-
|
Payments on
convertible debt
|
(419,055)
|
-
|
Payments on
shareholder advances
|
(5,000)
|
-
|
Payments on short
term debt
|
-
|
(255,000)
|
|
|
|
Net cash provided
by financing activities
|
1,775,570
|
1,371,934
|
|
|
|
Net increase in
cash
|
(151,143)
|
178,829
|
Cash, beginning of
period
|
179,032
|
203
|
|
|
|
CASH,
END OF PERIOD
|
$27,889
|
$179,032
|
|
|
|
Supplemental
disclosures of cash flow information:
|
|
|
Cash paid for
interest
|
$105,758
|
$9,920
|
Cash paid for
income taxes
|
$-
|
$-
|
The accompanying
notes are an integral part of these consolidated financial
statements.
F-6
Advanced
Medical Isotope Corporation
Notes
to Consolidated Financial Statements
For
the years ended December 31, 2016 and 2015
NOTE
1: ORGANIZATION & BASIS OF PRESENTATION
Business
Overview
In September of 2006, the Company began operating
as Advanced Medical Isotope Corporation (the
“Company”). The Company’s
predecessor was incorporated under the
laws of the state of Delaware in 1994. The Company has authorized
capital of 2,000,000,000 shares of common stock, $0.001 par value
per share, and 20,000,000 shares of preferred stock, $0.001 par
value per share.
Our
principal place of business is 1021 N Kellogg Street, Kennewick,
Washington, 99336. Our telephone number is (509) 736-4000. Our
corporate website address is http://www.isotopeworld.com. Our
common stock is currently listed for quotation on the OTC Pink
Marketplace under the symbol “ADMD.”
The
Company is a late stage radiation oncology medical device company
engaged in the development of its yttrium-90 based brachytherapy
device RadioGel™ for the treatment of non-resectable tumors.
A prominent team of radiochemists, scientists and engineers,
collaborating with strategic partners, including national
laboratories, universities and private corporations, lead the
Company’s development efforts. The Company’s overall
vision is to globally empower physicians, medical researchers and
patients by providing them with new isotope technologies that offer
safe and effective treatments for cancer.
The Company’s current focus is on the
development of its RadioGel™ device. RadioGel™ is an
injectable particle-gel, for brachytherapy radiation treatment of
cancerous tumors in people and animals. RadioGel™ is
comprised of a hydrogel, or a substance that is liquid at room
temperature and then gels when reaching body temperature after
injection into a tumor. In the gel are small, one micron,
yttrium-90 phosphate particles (“Y-90”). Once injected, these inert particles are
locked in place inside the tumor by the gel, delivering a very high
local radiation dose. The radiation is beta, consisting of
high-speed electrons. These electrons only travel a short distance
so the device can deliver high radiation to the tumor with minimal
dose to the surrounding tissue. Optimally, patients can go home
immediately following treatment without the risk of radiation
exposure to family members. Since Y-90 has a half-life of 2.7 days,
the radioactively drops to 5% of its original value after ten
days.
The Company’s lead brachytherapy products,
including RadioGel™, incorporate patented technology
developed for Battelle Memorial Institute
(“Battelle”) at Pacific Northwest National Laboratory,
a leading research institute for government and commercial
customers. Battelle has granted the Company an exclusive license to
patents covering the manufacturing, processing and applications of
RadioGel™ (the “Battelle
License”). Other
intellectual property protection includes proprietary production
processes and trademark protection in 17 countries. The Company
plans to continue efforts to develop new refinements on the
production process, and the product and application hardware, as a
basis for future patents.
The Company is currently focusing on obtaining
approval from the Food and Drug Administration
(“FDA”) to market and sell RadioGel™ as a
Class II medical device. The Company first requested FDA approval
of RadioGel™ in June 2013, at which time the FDA classified
RadioGel™ as a medical device. The Company is currently
developing test plans to address issues raised by the FDA in
connection with the Company’s previous submissions regarding
RadioGel™.The Company intends to request FDA approval to
apply for de novo classification of RadioGel™, which would
reclassify the device from a Class III device to a Class II device,
further simplifying the regulatory path.
F-7
In previous FDA submittals, the Company proposed
applying RadioGel™ for a very broad range of cancer
therapies, referred to as Indication for Use. The FDA has requested
that the Company reduce its Indications for Use. To comply with
that request, the Company has expanded its Medical Advisory Board
(“MAB”) and engaged doctors from respected
hospitals who have evaluated the candidate cancer therapies based
on three criteria: (1) potential for FDA approval and successful
therapy; (2) notable advantage over current therapies; and (3)
probability of wide spread acceptance by the medical
community.
The
MAB selected eighteen applications for RadioGel™, each of
which meet the criteria described above. This large number confirms
the wide applicability of the device and defines the path for
future business growth. The Company intends to apply to the FDA for
a single Indication for Use, followed by subsequent applications
for additional Indications for Use. The initial application should
facilitate each subsequent application, and the testing for many of
the subsequent applications could be conducted in parallel,
depending on available resources.
The
MAB selected the treatment of basal cell and squamous cell skin
cancers for the first Indication for Use to be submitted to the
FDA. According to the American Cancer Society, one out of every
three new cancers diagnosed in the U.S. is a cancerous skin lesion
of this type, representing 5.5 million tumors diagnosed annually.
The MAB believes RadioGel™ has the potential to be the
preferred treatment in a reasonable number of cases in a very large
market.
The
Company’s, IsoPet Solutions division was established in May
2016 to focus on the veterinary oncology market. The Company has
engaged four different university veterinarian hospitals to begin
using RadioGel™ for treatment of four different cancer types
in dogs and cats. Washington State University Veterinary Hospital
has tested one cat to demonstrate the procedures and the absence of
any significant toxicity effect. The other three centers are
expected to begin therapy during the second quarter of 2017 after
their internal administrative review process is
completed.
These
animal therapies will focus on creating labels that describe the
procedures in detail as a guide to future veterinarians. The labels
will be voluntarily submitted to the FDA for review. They will then
be used as data for future FDA applications in the medical sector
and as key intellectual property for licensing to private
veterinary clinics. In 2018, Dr. Alice Villalobos, the Chair of our
Veterinarian Advisory Board, will be the first licensee of these
therapies in her private clinic to demonstrate the business
model.
The
Company anticipates that future profit will be derived from direct
sales of RadioGel™ and related services, and from licensing
to private medical and veterinary clinics in the U.S. and
internationally.
Going
Concern
The accompanying
financial statements have been prepared on a going concern basis,
which contemplates the realization of assets and satisfaction of
liabilities in the normal course of business. As shown
in the accompanying financial statements, the Company has suffered
recurring losses and used significant cash in support of its
operating activities and the Company’s cash position is not
sufficient to support the Company’s operations. Research and development of the Company’s
brachytherapy product line has been funded with proceeds from the
sale of equity and debt securities as well as a series of grants.
The Company requires funding of approximately $1.5 million annually
to maintain current operating activities. Over the next 12 to 24
months, the Company believes it will cost approximately $5.0
million to $10.0 million to fund: (1) the FDA approval process and
initial deployment of the brachytherapy products, and (2) initiate
regulatory approval processes outside of the United States. The
continued deployment of the brachytherapy products and a worldwide
regulatory approval effort will require additional resources and
personnel. The principal variables in the timing and amount of
spending for the brachytherapy products in the next 12 to 24 months
will be the FDA’s classification of the Company’s
brachytherapy products as Class II or Class III devices (or
otherwise) and any requirements for additional studies which may
possibly include clinical studies. Thereafter, the principal
variables in the amount of the Company’s spending and its
financing requirements would be the timing of any approvals and the
nature of the Company’s arrangements with third parties for
manufacturing, sales, distribution and licensing of those products
and the products’ success in the U.S. and elsewhere. The
Company intends to fund its activities through strategic
transactions such as licensing and partnership agreements or
additional capital raises.
F-8
Following
receipt of required regulatory approvals and financing, in the
U.S., the Company intends to outsource material aspects of
manufacturing, distribution, sales and marketing. Outside of the
U.S., the Company intends to pursue licensing arrangements and/or
partnerships to facilitate its global commercialization
strategy.
In
the longer-term, subject to the Company receiving adequate funding,
regulatory approval for RadioGel™ and other brachytherapy
products, and thereafter being able to successfully commercialize
its brachytherapy products, the Company intends to consider
resuming research efforts with respect to other products and
technologies intended to help improve the diagnosis and treatment
of cancer and other illnesses
Based
on the Company’s financial history since inception, its
auditor has expressed substantial doubt as to the Company’s
ability to continue as a going concern. The Company has limited
revenue, nominal cash, and has accumulated deficits since
inception. If the Company cannot obtain sufficient additional
capital, the Company will be required to delay the implementation
of its business strategy and may not be able to continue
operations.
As of December 31,
2016 the Company has $27,889 cash on hand. There are currently
commitments to vendors for products and services purchased, plus,
the employment agreements of the CFO and other employees of the
Company and the Company’s current lease commitments that will
necessitate liquidation of the Company if it is unable to raise
additional capital. The current level of cash is not enough to
cover the fixed and variable obligations of the
Company.
Assuming the
Company is successful in the Company’s sales/development
effort, it believes that it will be able to raise additional funds
through strategic agreements or the sale of the Company’s
stock to either current or new stockholders. There is no guarantee
that the Company will be able to raise additional funds or to do so
at an advantageous price.
The financial
statements do not include any adjustments relating to the
recoverability and classification of liabilities that might be
necessary should the Company be unable to continue as a going
concern. The Company’s continuation as a going
concern is dependent upon its ability to generate sufficient cash
flow to meet its obligations on a timely basis and ultimately to
attain profitability. The Company plans to seek
additional funding to maintain its operations through debt and
equity financing and to improve operating performance through a
focus on strategic products and increased efficiencies in business
processes and improvements to the cost structure. There
is no assurance that the Company will be successful in its efforts
to raise additional working capital or achieve profitable
operations. The financial statements do not include any
adjustments that might result from the outcome of this
uncertainty.
F-9
NOTE
2: SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Use
of Estimates
The preparation of
financial statements in accordance with generally accepted
accounting principles requires management to make estimates and
assumptions that affect the reported amounts of assets and
liabilities and the disclosure of contingent assets and liabilities
at the date of financial statements and the reported amounts of
revenues and expenses during the reporting
period. Actual results could differ from those
estimates.
Principles
of Consolidation
The accompanying consolidated financial statements
include the accounts of Advanced Medical Isotope Corporation
and its wholly-owned subsidiary
IsoPet Solutions Corporation (“Iso-Pet”). All significant inter-company balances and
transactions have been eliminated in
consolidation.
Financial
Statement Reclassification
Certain
account balances from prior periods have been reclassified in these
audited consolidated financial statements so as to conform to
current period classifications.
Cash
Equivalents
For the purposes of
the statement of cash flows, the Company considers all highly
liquid debt instruments purchased with an original maturity of
three months or less to be cash equivalents.
Inventory
Inventory is
reported at the lower of cost or market, determined using the
first-in, first-out basis, or net realizable value. All inventories
consist of finished goods. The Company had no raw materials or work
in process. The Company had been carrying inventory consisting of
two bottles of O-18 water for a value of $8,475. The Company
determined this water was no longer usable and wrote off the $8,475
value as of December 31, 2016.
Fair
Value of Financial Instruments
Fair Value of
Financial Instruments, requires disclosure of the fair value
information, whether or not recognized in the balance sheet, where
it is practicable to estimate that value. As of December 31, 2016
and December 31, 2015, the balances reported for cash, prepaid
expenses, accounts receivable, accounts payable, and accrued
expenses, approximate the fair value because of their short
maturities.
Fair value is
defined as the price that would be received to sell an asset or
paid to transfer a liability in an orderly transaction between
market participants at the measurement date. ASC Topic 820
established a three-tier fair value hierarchy which prioritizes the
inputs used in measuring fair value. The hierarchy gives the
highest priority to unadjusted quoted prices in active markets for
identical assets or liabilities (level 1 measurements) and the
lowest priority to unobservable inputs (level 3 measurements).
These tiers include:
Level 1, defined as
observable inputs such as quoted prices for identical instruments
in active markets;
Level 2, defined as
inputs other than quoted prices in active markets that are either
directly or indirectly observable such as quoted prices for similar
instruments in active markets or quoted prices for identical or
similar instruments in markets that are not active;
and
Level 3, defined as
unobservable inputs in which little or no market data exists,
therefore requiring an entity to develop its own assumptions, such
as valuations derived from valuation techniques in which one or
more significant inputs or significant value drivers are
unobservable.
F-10
The Company
measures certain financial instruments at fair value on a recurring
basis. Assets and liabilities measured at fair value on a recurring
basis were calculated using the Black-Scholes pricing model and are
as follows at December 31, 2016:
|
Total
|
Level
1
|
Level
2
|
Level
3
|
Assets:
|
|
|
|
|
Total Assets
Measured at Fair Value
|
$-
|
$-
|
$-
|
$-
|
|
|
|
|
|
Liabilities:
|
|
|
|
|
Derivative
Liability
|
324,532
|
-
|
-
|
324,532
|
Total Liabilities
Measured at Fair Value
|
$324,532
|
$-
|
$-
|
$324,532
|
Assets and
liabilities measured at fair value on a recurring basis are as
follows at December 31, 2015:
|
Total
|
Level 1
|
Level 2
|
Level 3
|
Assets
|
|
|
|
|
Total Assets
Measured at Fair Value
|
$-
|
$-
|
$-
|
$-
|
|
|
|
|
|
Liabilities
|
|
|
|
|
Liability for lack
of authorized shares
|
852,091
|
-
|
-
|
852,091
|
Derivative
Liability
|
4,235,016
|
-
|
-
|
4,235,016
|
Total Liabilities
Measured at Fair Value
|
$5,087,107
|
$-
|
$-
|
$5,087,107
|
Fixed
Assets
Fixed assets are
carried at the lower of cost or net realizable value. Production
equipment with a cost of $2,500 or greater and other fixed assets
with a cost of $1,500 or greater are capitalized. Major betterments
that extend the useful lives of assets are also capitalized. Normal
maintenance and repairs are charged to expense as incurred. When
assets are sold or otherwise disposed of, the cost and accumulated
depreciation are removed from the accounts and any resulting gain
or loss is recognized in operations.
Depreciation is
computed using the straight-line method over the following
estimated useful lives:
Production
equipment:
|
3 to 7
years
|
Office
equipment:
|
2 to 5
years
|
Furniture and
fixtures:
|
2 to 5
years
|
Leasehold
improvements and capital lease assets are amortized over the
shorter of the life of the lease or the estimated life of the
asset.
Management of the
Company reviews the net carrying value of all of its equipment on
an asset by asset basis whenever events or changes in circumstances
indicate that its carrying amount may not be recoverable. These
reviews consider the net realizable value of each asset, as
measured in accordance with the preceding paragraph, to determine
whether impairment in value has occurred, and the need for any
asset impairment write-down.
License
Fees
License fees are
stated at cost, less accumulated amortization. Amortization of
license fees is computed using the straight-line method over the
estimated economic useful life of the assets.
F-11
The Company made a
$10,000 investment in 2010 for an exclusive license with Battelle
Memorial Institute regarding its technology for the production of a
Brachytherapy seed. In August 2010 the Company entered into a
License Agreement for the Patent Rights in the area of a
Brachytherapy seed with a Fast-dissolving Matrix for Optimized
Delivery of Radionuclides. This Agreement calls for a $10,000
nonrefundable fee upon execution, a royalty agreement on sales and
on funds received from any sublicenses. The $10,000 nonrefundable
fee paid upon execution was capitalized as License Fees and is
amortized on the straight-line basis over a three-year life.
Additionally the Agreement calls for a minimum annual
fee.
The Company agreed
for a mutual termination of this license effective December 31,
2016 and that the $25,000 minimum annual fee for 2016 due January
2017 would not be owed. The Company was carrying $35,482 in patent
costs relating to this license, which was written off as impaired
assets during the twelve months ended December 31, 2016. The
Company still has a $7,026 balance owed for patent expense accrued
during 2016.
Calendar
Year
|
Minimum
Royalties per Calendar Year
|
|
2010
|
$-
|
|
2011
|
$-
|
|
2012
|
$2,500
|
|
2013
|
$5,000
|
(1)
|
2014
|
$7,500
|
(2)
|
2015
|
$10,000
|
(3)
|
2016 and each
calendar year thereafter
|
$25,000
|
(4)
|
|
|
|
(1) Paid February,
2014
|
|
|
(2) Paid February,
2015
|
|
|
(3) Paid February,
2016
|
|
|
(4) No longer owed
due to termination of license agreement effective December 31,
2016
|
|
|
The Company made a
$5,000 investment in February 2011 for a one-year option agreement
to negotiate an exclusive license agreement with Battelle Memorial
Institute regarding its patents for the production of
RadioGel™. This option agreement calls for a
$5,000 upfront fee for the option, which expired February 2012 and
was fully expensed in the twelve months ended December 31,
2011. Effective March 2012, the Company entered into an
exclusive license agreement with Battelle Memorial Institute
regarding the use of its patented RadioGel™ technology. This
license agreement calls for a $17,500 nonrefundable license fee and
a royalty based on a percent of gross sales for licensed products
sold; the license agreement also contains a minimum royalty amount
to be paid each year starting with 2013.
Calendar
Year
|
Minimum
Royalties per Calendar Year
|
|
2012
|
$-
|
|
2013
|
$5,000
|
(1)
|
2014
|
$7,500
|
(2)
|
2015
|
$10,000
|
(3)
|
2016
|
$10,000
|
(4)
|
2017 and each
calendar year thereafter
|
$25,000
|
|
(1) Paid February,
2014
|
|
|
(2) Paid February,
2015
|
|
|
(3) Paid February,
2016
|
|
|
(4) $5,399 was paid
January 2017 and the remaining $4,601 was paid February
2017.
|
|
|
F-12
The Company
periodically reviews the carrying values of capitalized license
fees and any impairments are recognized when the expected future
operating cash flows to be derived from such assets are less than
their carrying value.
Amortization is
computed using the straight-line method over the estimated useful
live of three years. Amortization of license fees was $0, and
$1,339 for the years ended December 31, 2016, and 2015,
respectively.
Patents
and Intellectual Property
The Company had a
total $35,482 of capitalized patents and intellectual property
costs at December 31, 2015 for the patent rights in the area of a
Brachytherapy seed with a Fast-dissolving Matrix for Optimized
Delivery of Radionuclides. Effective December 31, 2016 the Company
agreed to terminate this non-utilized patent license for which the
$35,482 of capitalized patent and intellectual costs applied and
therefore the Company wrote off $35,482 of capitalized costs in the
twelve months ending December 31, 2016.
Revenue
Recognition
The Company
recognized revenue related to product sales when (i) persuasive
evidence of the arrangement exists, (ii) shipment has occurred,
(iii) the fee is fixed or determinable, and (iv) collectability is
reasonably assured.
Revenue for the
fiscal year ended December 31, 2016 and December 31, 2015 consisted
of consulting revenue. The Company recognizes revenue once an order
has been received and shipped to the customer or services have been
performed. Prepayments, if any, received from customers prior to
the time products are shipped are recorded as deferred revenue. In
these cases, when the related products are shipped, the amount
recorded as deferred revenue is recognized as revenue. The Company
does not accrue for sales returns and other allowances as it has
not experienced any returns or other allowances.
Income
from Grants and Deferred Income
Government grants
are recognized when all conditions of such grants are fulfilled or
there is reasonable assurance that they will be fulfilled. The
Company has chosen to recognize income from grants as it incurs
costs associated with those grants, and until such time as it
recognizes the grant as income those funds received will be
classified as deferred income on the balance sheet.
On September 1,
2015, the Company received notification it had been awarded from
Washington State University, $42,019 grant funds from the sub-award
project entitled “Optimized Injectable Radiogels for
High-dose Therapy of Non-Resectable Solid Tumors”. The
Company received $21,010 and $21,009 of the grand award in the
twelve months ended December 31, 2016 and 2015,
respectively.
Earnings
(Loss) Per Share
The Company
accounts for its earnings (loss) per common share by replacing
primary and fully diluted earnings per share with basic and diluted
earnings per share. Basic earnings (loss) per share is computed by
dividing income (loss) available to common stockholders (the
numerator) by the weighted-average number of common shares
outstanding (the denominator) for the period, and does not include
the impact of any potentially dilutive common stock equivalents
since the impact would be anti-dilutive. The computation of diluted
earnings per share is similar to basic earnings per share, except
that the denominator is increased to include the number of
additional common shares that would have been outstanding if
potentially dilutive common shares had been issued. However, since
the Company does not have sufficient authorized shares of common
stock, we did not include these in our calculation.
F-13
Securities, all of
which represent common stock equivalents, that could be dilutive in
the future as of December 31, 2016 and 2015, are as
follows:
|
December
31, 2016
|
December
31, 2015
|
Convertible
debt
|
6,441,644
|
7,848,421
|
Preferred
stock
|
37,735,920
|
16,270,000
|
Common stock
options
|
2,402,500
|
51,350
|
Common stock
warrants
|
3,579,505
|
6,791,003
|
Total potential
dilutive securities
|
50,159,569
|
30,960,774
|
Research
and Development Costs
Research and
developments costs, including salaries, research materials,
administrative expenses and contractor fees, are charged to
operations as incurred. The cost of equipment used in research and
development activities which has alternative uses is capitalized as
part of fixed assets and not treated as an expense in the period
acquired. Depreciation of capitalized equipment used to perform
research and development is classified as research and development
expense in the year computed.
The Company
incurred $328,026 and $149,650 research and development costs for
the years ended December 31, 2016, and 2015, respectively, all of
which were recorded in the Company’s operating expenses noted
on the income statements for the years then ended.
Advertising
and Marketing Costs
Advertising and
marketing costs are expensed as incurred except for the cost of
tradeshows which are deferred until the tradeshow occurs. Tradeshow
expenses incurred and not expensed as of the years ended December
31, 2016, and 2015 were $0 and $14,800, respectively. During the
twelve months ended December 31, 2016 and 2015, the Company
incurred $284,138 and $0, respectively, in advertising and
marketing costs.
Shipping
and Handling Costs
Shipping and
handling costs are expensed as incurred and included in cost of
materials.
Legal
Contingencies
In the ordinary
course of business, the Company is involved in legal proceedings
involving contractual and employment relationships, product
liability claims, patent rights, and a variety of other matters.
The Company records contingent liabilities resulting from asserted
and unasserted claims against it, when it is probable that a
liability has been incurred and the amount of the loss is
reasonably estimable. The Company discloses contingent liabilities
when there is a reasonable possibility that the ultimate loss will
exceed the recorded liability. Estimated probable losses require
analysis of multiple factors, in some cases including judgments
about the potential actions of third-party claimants and courts.
Therefore, actual losses in any future period are inherently
uncertain. Currently, the Company does not believe any probable
legal proceedings or claims will have a material impact on its
financial position or results of operations. However, if actual or
estimated probable future losses exceed the Company’s
recorded liability for such claims, it would record additional
charges as other expense during the period in which the actual loss
or change in estimate occurred.
There had been an
ongoing dispute with the landlord, Rob and Maribeth Myers,
regarding the production center rent. During 2016, the
Company reached a Settlement Agreement with regards to this dispute
resulting in a payment of $438,830 for rent, interest, and
costs.
F-14
There is an ongoing
dispute with BancLeasing and Washington Trust Bank regarding
application of lease payments to the principal loan amount for the
linear accelerator, and the Company believed it overpaid by
approximately $300,000. In 2016 the Company was awarded in the
Superior Court of the State of Washington a total sum of $527,876
against BancLeasing. The Company is pursuing its options for
collection of the awarded amount, however there can be no assurance
as to any eventual collection.
Income Taxes
To address
accounting for uncertainty in tax positions, the Company clarifies
the accounting for income taxes by prescribing a minimum
recognition threshold that a tax position is required to meet
before being recognized in the financial statements. The Company
also provides guidance on de-recognition, measurement,
classification, interest, and penalties, accounting in interim
periods, disclosure and transition.
The Company files
income tax returns in the U.S. federal jurisdiction, and
Delaware. The Company did not have any tax expense for
the years ended December 31, 2016 and 2015. The Company
did not have any deferred tax liability or asset on its balance
sheet on December 31, 2016 and 2015.
Interest costs and
penalties related to income taxes, if any, will be classified as
interest expense and general and administrative costs,
respectively, in the Company’s financial statements. For the
years ended December 31, 2016 and 2015, the Company did not
recognize any interest or penalty expense related to income taxes.
The Company believes that it is not reasonably possible for the
amounts of unrecognized tax benefits to significantly increase or
decrease within the next 12 months.
Stock-Based
Compensation
The Company
recognizes in the financial statements compensation related to all
stock-based awards, including stock options, based on their
estimated grant-date fair value. The Company has estimated expected
forfeitures and is recognizing compensation expense only for those
awards expected to vest. All compensation is recognized by the time
the award vests.
The Company
accounts for equity instruments issued in exchange for the receipt
of goods or services from non-employees. Costs are measured at the
fair market value of the consideration received or the fair value
of the equity instruments issued, whichever is more reliably
measurable. The value of equity instruments issued for
consideration other than employee services is determined on the
earlier of the date on which there first exists a firm commitment
for performance by the provider of goods or services or on the date
performance is complete. The Company recognizes the fair
value of the equity instruments issued that result in an asset or
expense being recorded by the Company, in the same period(s) and in
the same manner, as if the Company has paid cash for the goods or
services.
Recent
Accounting Pronouncements
There are no
recently issued accounting pronouncements that the Company believes
are applicable or would have a material impact on the financial
statements of the Company.
Reclassifications
Certain prior-year
amounts have been reclassified to conform with current year’s
presentation.
F-15
NOTE
3: FIXED ASSETS
Fixed assets
consist of the following at December 31, 2016 and
2015:
|
December
31, 2016
|
December
31, 2015
|
Production
equipment
|
$15,182
|
$1,938,532
|
Building
|
-
|
446,772
|
Leasehold
improvements
|
-
|
3,235
|
Office
equipment
|
14,594
|
32,769
|
|
29,776
|
2,421,308
|
Less accumulated
depreciation
|
(28,303)
|
(2,416,888)
|
|
$1,473
|
$4,420
|
Depreciation
expense for the above fixed assets for the years ended December 31,
2016 and 2015, respectively, was $2,947 and $4,332.
During the year
ended December 31, 2016, the Company abandoned production
equipment, building, leasehold improvements, and office equipment
with an original cost totaling $1,016,532 that had been located in
the production center. Additionally the Company removed the linear
accelerator form the production center and has placed the equipment
into storage. The $1,375,000 original cost of the linear
accelerator was also written off during the year ended December 31,
2016. All of the equipment written off during the year ended
December 31, 2016 had been fully depreciated.
NOTE 4: INTANGIBLE ASSETS
Intangible assets
consist of the following at December 31, 2016 and December 31,
2015:
|
December
31, 2016
|
December
31, 2015
|
License
Fee
|
$112,500
|
$112,500
|
Less accumulated
amortization
|
(112,500)
|
(112,500)
|
|
-
|
-
|
Patents and
intellectual property
|
-
|
35,482
|
|
$-
|
$35,482
|
Amortization
expense for the above intangible assets for the years ended
December 31, 2016 and 2015, respectively, was $0 and
$1,339.
NOTE 5: DEBT ISSUANCE COSTS
During the years
ending December 31, 2016 and 2015, the Company paid $0 and $5,000,
respectively, in cash for debt arrangements.
The Company
amortizes debt issuance costs on a straight-line basis over the
life of the debt arrangements and recognized $0, and $18,917,
during the years ending December 31, 2016, and 2015,
respectively.
F-16
During the twelve
months ending December 31, 2016 and 2015 the Company had the
following activity in their debt issuance cost
account:
Debt issuance costs
at December 31, 2014
|
$13,917
|
Cash paid as fees
for debt arrangements
|
5,000
|
Amortization of
debt issuance costs
|
(18,917)
|
Debt issuance costs
at December 31, 2015
|
-
|
Cash paid as fees
for debt arrangements
|
-
|
Amortization of
debt issuance costs
|
-
|
Debt issuance costs
at December 31, 2016
|
$-
|
NOTE
6: RELATED PARTY TRANSACTIONS
Related
Party Promissory Notes
As of December 31,
2016 and 2015, the Company had the following related party
promissory notes outstanding:
|
December 31,
2016
|
December 31,
2015
|
||
|
Principal
(net)
|
Accrued
Interest
|
Principal
(net)
|
Accrued
Interest
|
September 2015
$1,055,535 Note, 8% interest, due on demand after March
2017
|
$-
|
$-
|
$1,055,535
|
27,299
|
September 2015
$142,415 Note, 10% interest, due May 2016
|
-
|
-
|
142,415
|
4,669
|
October 2015
$82,500 Note, 10% interest due October 2016
|
82,500
|
10,239
|
82,500
|
1,966
|
February 2016
$50,000 Note, 10% interest, due February
2017
|
50,000
|
4,192
|
-
|
-
|
May 2016
$109,695 Note, 10% interest, due July 2017
|
109,695
|
7,093
|
-
|
-
|
May 2016
$90,000 Note, 10% interest, due May 2017
|
90,000
|
5,425
|
-
|
-
|
Total Convertible
Notes Payable, Net
|
$332,195
|
$26,949
|
$1,280,450
|
$33,934
|
During the year
ending December 31, 2016, the Company received proceeds from new
related party promissory notes of $249,695 and recorded conversions
of $1,197,950 for related party note principal.
During the year
ending December 31, 2015 the Company received proceeds from new
related party promissory notes of $224,915. Additionally, in
September of 2015 multiple convertible notes were rolled in
together for a total new non-convertible promissory note of
$1,055,532.
Related
Party Convertible Notes Payable
During the year
ending December 31, 2016, the Company received proceeds from new
related party convertible notes of $473,613 and, at inception,
issued 37,906 shares of Series A Convertible Preferred Stock
(“Series A
Preferred”) as loan fees valued at $29,156. Each of
the Company’s related party convertible notes have a
conversion rate that is variable, therefore the Company has
accounted for such conversion features as derivative instruments
(see Note 9). As a result of recording the preferred stock and the
derivative liabilities at note inception, the Company increased the
debt discount recorded on their convertible notes by $473,613 and
recorded $1,912,587 in additional interest expense. During the year
ending December 31, 2016, the Company recorded amortization of
$25,000 on their related party convertible note debt discounts,
recorded conversions of $473,613 for related party note principal,
and recorded $448,613 of debt discount write-offs for early debt
conversion. As a result of all related party convertible notes
being converted during the year ending December 31, 2016, the
related party convertible notes payable balance was $0 as of
December 31, 2016.
F-17
During the year
ending December 31, 2015, the Company received proceeds from new
related party convertible notes of $156,500. Of that $156,500,
$113,500 was convertible at a fixed rate and $43,000 was
convertible at a variable rate.
The new related
party convertible notes of $113,500 were convertible into the
Company’s common stock at $0.001 per share. The convertible
notes were issued with 43,326 shares of common stock (see Note 11),
therefore the Company recorded debt discounts at inception of
$4,896 to allocate the convertible note proceeds to the common
stock. In September of 2015, the $113,500 of new convertible notes
were rolled in together with multiple other notes for a total new
promissory note of $1,055,532 which was not convertible. The $4,896
of debt discounts were fully amortized prior to the convertible
notes being rolled into the promissory note.
The new related
party convertible notes of $43,000 were issued with 3,440 shares of
Series A preferred stock as loan fees valued at $17,401 (see Note
11). Each of these related party convertible notes have a
conversion rate that is variable, therefore the Company has
accounted for such conversion features as derivative instruments
(see Note 9). As a result of recording the preferred stock and the
derivative liabilities at note inception, the Company increased the
debt discount recorded on these convertible notes by $43,000 and
recorded $17,401 in additional interest expense. During the year
ending December 31, 2016 the Company recorded amortization of
$43,000 on these related party convertible note debt discounts and
recorded conversions of $43,000 for related party note
principal.
During the year
ending December 31, 2015, the Company recorded additional
conversions of $3,638,566 of note principal and amortization of
$6,328 of debt discounts for related party convertible notes that
had been outstanding as of December 31, 2014.
As a result of all
related party convertible notes being rolled into a non-convertible
promissory note or converted during the year ending December 31,
2015 the related party convertible notes payable balance was $0 as
of December 31, 2015.
Preferred
Shares Issued to Officers
During 2016, the
Company issued 10,000 shares of its Series A Preferred to its CFO,
representing $54,152, for services (see Note 11).
During 2015, the
Company issued the CEO and CFO a combined total of 175,000 shares
of Series A Preferred in exchange for a combined total of $262,500
of accrued and unpaid wages (see Note 11).
Rent
Expenses
On July 17, 2007,
the Company entered into a five-year lease for its production
center from a less than 5% shareholder. Subsequent to July 31,
2012, the Company was renting this space on a month-to-month basis
at $11,904 per month. Effective January 1, 2015, the
Company’s lease was terminated. There has been an ongoing
dispute with the landlord, Rob and Maribeth Myers, regarding the
production center rent. During 2016, the Company reached
a Settlement Agreement with regards to this dispute resulting in a
payment of $438,830 for rent, interest, and costs.
The Company rents
office space from a significant shareholder and director of the
Company on a month-to-month basis with a monthly payment of
$1,500.
Rental expense for
the years ended December 31, 2016 and 2015 consisted of the
following:
|
Year ended
December 31, 2016
|
Year ended December
31, 2015
|
Office and
warehouse space
|
$40,000
|
$155,306
|
Corporate
office
|
18,000
|
18,000
|
Total Rental
Expense
|
$58,000
|
$173,306
|
F-18
NOTE
7: CAPITAL LEASE OBLIGATIONS
During September
2007, the Company obtained two master lease agreements for
$1,875,000 and $631,000, with interest on both leases accruing at
8.6% annually, secured by equipment and personal guarantee of two
of the major stockholders. These long-term agreements shall be
deemed capital lease obligations for purposes of financial
statement reporting. The purpose of the lease is to acquire a
Pulsar 10.5 PET Isotope Production System plus ancillary
equipment.
This capital lease
and its resulting obligation is recorded at an amount equal to the
present value at the beginning of the lease term of minimum lease
payments during the lease term, excluding any portion of the
payments representing taxes to be paid by the Company. This amount
does not exceed the fair value of the leased property at the lease
inception, so the recorded amount is the fair value.
The lease requires
the Company to maintain a minimum debt service coverage ratio of
1:1 measured at fiscal year-end. Non-compliance with this provision
shall constitute a default and guarantors must contribute capital
sufficient to fund any deficit in the debt service coverage
ratio.
The Company fully
paid this capital lease obligations during the twelve months ending
December 31, 2015; however there is an ongoing dispute with the
lessor as the Company believes it has overpaid its lease
obligations.
NOTE
8: CONVERTIBLE NOTES PAYABLE
As of December 31,
2016 and 2015, the Company had the following convertible notes
outstanding:
|
December 31,
2016
|
December 31,
2015
|
||
|
Principal
(net)
|
Accrued
Interest
|
Principal
(net)
|
Accrued
Interest
|
July and August
2012 $1,060,000 Notes convertible into common stock at $4.60 per
share, 12% interest, due December 2013 and January
2014
|
$95,000
|
$50,365
|
$165,000
|
69,712
|
January 2014
$50,000 Note convertible into common stock at a variable conversion
price, 8% interest, due January 2015
|
-
|
-
|
50,000
|
7,682
|
January 2014
$55,500 Note convertible into common stock at a variable
conversion price, 10% interest, due October 2014
|
-
|
-
|
10,990
|
5,457
|
February 2014
$46,080 Note convertible into common stock at a variable conversion
price, 10% interest, due February 2015
|
-
|
-
|
-
|
2,358
|
February 2014
$27,800 Note convertible into common stock at a variable conversion
price, 10% one-time interest, due February 2015
|
-
|
-
|
20,000
|
-
|
March 2014 $50,000
Note convertible into common stock at a variable conversion price,
10% interest, due March 2015
|
-
|
-
|
36,961
|
6,572
|
March 2014
$165,000 Note convertible into common stock at a variable
conversion price, 10% interest, due April 2015
|
-
|
-
|
61,301
|
24,109
|
April 2014
$32,000 Note convertible into common stock at a variable
conversion price, 10% interest, due April 2015
|
-
|
-
|
22,042
|
3,034
|
April 2014 $46,080
Note convertible into common stock at a variable conversion price,
10% interest due April 2015
|
-
|
-
|
5,419
|
4,608
|
May 2014
$55,000 Note convertible into common stock at a variable
conversion price, 12% interest, due May 2015
|
-
|
-
|
25,000
|
1,836
|
June 2014 $28,800
Note convertible into common stock at a variable conversion price,
10% interest due June 2015
|
-
|
-
|
28,800
|
2,880
|
June 2014 $40,000
Note convertible into common stock at a variable conversion price,
10% interest, due June 2015
|
-
|
-
|
40,000
|
6,049
|
June 2014 $40,000
Note convertible into common stock at a variable conversion price,
10% interest, due June 2015
|
-
|
-
|
38,689
|
5,851
|
June 2014 $56,092
Note convertible into common stock at a variable conversion price,
16% interest, due July 2015
|
-
|
-
|
56,092
|
13,462
|
July 2014 $37,500
Note convertible into common stock at a variable conversion price,
12% interest, due July 2015
|
-
|
-
|
37,015
|
6,377
|
August 2014 $36,750
Note convertible into common stock at a variable conversion price,
10% interest, due April 2015
|
-
|
-
|
36,750
|
5,538
|
August 2014
$33,500 Note convertible into common stock at a variable
conversion price, 4% interest, due February 2015
|
-
|
-
|
33,500
|
-
|
September 2014
$37,500 Note convertible into common stock at a variable conversion
price, 12% interest, due September 2015
|
-
|
-
|
36,263
|
5,576
|
May through October
2015 $605,000 Notes convertible into preferred stock at $1 per
share, 8-10% interest, due September 30, 2015
|
-
|
17,341
|
-
|
18,264
|
October through
December 2015 $613,000 Notes convertible into preferred stock at $1
per share, 8% interest, due June 30, 2016, net of debt discount of
$0 and $560,913, respectively
|
-
|
5,953
|
52,087
|
2,519
|
January through
March 2016 $345,000 Notes convertible into preferred stock at $1
per share, 8% interest, due June 30, 2016
|
-
|
696
|
-
|
-
|
November 2016
$979,162 Notes convertible into common stock at a variable
conversion price, 10% interest, due May 2017, net of debt discounts
of $540,720 and $0, respectively
|
438,442
|
12,397
|
-
|
-
|
Penalties on
notes in default
|
11,066
|
-
|
1,032,475
|
-
|
Total Convertible
Notes Payable, Net
|
$544,508
|
$86,752
|
$1,788,384
|
$191,884
|
F-19
During the year
ending December 31, 2016, the Company received proceeds from new
convertible notes of $1,273,534, obtained advances from
shareholders of $127,533 that were reclassified into convertible
notes payable, and reclassified $455,150 of accrued interest into
convertible notes payable. The Company recorded original issue
discounts and loan fees on new convertible notes of $193,831 and
$6,000, respectively, which also increased the debt discounts
recorded on the convertible notes. The Company recorded $419,055 of
payments on their convertible notes, conversions of $1,444,950 of
convertible note principal, a total gain on settlement of
$1,456,113 representing the write-off of convertible note
principal, and $814,625 of debt discount write-offs for early debt
conversion or extinguishment. Each of the Company’s
convertible notes have a conversion rate that is variable. The
Company therefore has accounted for such conversion features as
derivative instruments (see Note 9). As a result of recording
derivative liabilities at note inception, the Company increased the
debt discount recorded on their convertible notes by $809,835
during the year ending December 31, 2016. The Company also recorded
amortization of $579,042 on their convertible note debt discounts.
Lastly, the Company issued 347,400 shares of Series A Preferred as
loan fees with their new convertible notes. The Company therefore
increased their convertible note debt discount by $363,807, which
represented the portion of the convertible note proceeds that were
allocated to preferred stock.
During the year
ending December 31, 2015, the Company received proceeds from new
convertible notes of $1,285,000, recorded default penalties on new
convertible notes of $116,521, and recorded original issue
discounts of $5,000, which also increased the debt discounts
recorded on the convertible notes. The Company recorded $255,000 of
payments on their convertible notes conversions of $584,700 of
convertible note principal, a total loss on settlement of $967,038
representing the write-off of convertible note principal, and
$3,035 of debt discount write-offs for early debt conversion or
extinguishment. Each of the Company’s convertible notes have
a conversion rate that is variable. The Company therefore has
accounted for such conversion features as derivative instruments
(see Note 9). As a result of recording derivative liabilities at
note inception, the Company has increased the debt discount
recorded on their convertible notes by $1,285,000 during the year
ending December 31, 2015. The Company also recorded amortization of
$1,031,443 on their convertible note debt discounts.
NOTE
9: DERIVATIVE LIABILITY
During the years
ending December 31, 2016 and 2015, the Company had the following
activity in their derivative liability account:
|
Warrants
|
Conversion
Feature
|
Total
|
Derivative
Liability at December 31, 2014
|
1,263,929
|
10,238,451
|
11,502.380
|
Derivative
Liability Recorded on New Instruments
|
-
|
698,705
|
698,705
|
Elimination of
Liability on Conversion
|
-
|
(79,044)
|
(79,044)
|
Change in Fair
Value
|
(549,528)
|
(7,337,497)
|
(7,887,025)
|
Derivative
Liability at December 31, 2015
|
714,401
|
3,520,615
|
4,235,016
|
Derivative
Liability Recorded on New Instruments
|
-
|
6,150,026
|
6,150,026
|
Elimination of
Liability on Conversion
|
(1,266,795)
|
(10,381,138)
|
(11,647,933)
|
(Gain) on
Settlement of Debt
|
-
|
(656,930)
|
(656,930)
|
Change in Fair
Value
|
552,452
|
1,691,901
|
(2,244,353)
|
Derivative
Liability at December 31, 2016
|
58
|
324,474
|
324,532
|
The Company uses
the Black-Scholes pricing model to estimate fair value for those
instruments convertible into common stock at inception, at
conversion date, and at each reporting date. During the
year ending December 31, 2016, and 2015, the Company used the
following assumptions in their Black-Scholes model:
|
|
December 31,
2016
|
|
|
December 31,
2015
|
|
||||||||||
|
|
Warrants
|
|
|
Conversion
Feature
|
|
|
Warrants
|
|
|
Conversion
Feature
|
|
||||
Risk-free interest
rate
|
|
|
0.46% - 1.38%
|
|
|
|
0.12% -
0.85%
|
|
|
|
0.65% - 1.31%
|
|
|
|
0.02% -
0.25%
|
|
Expected life in
years
|
|
|
0.53 -
4.08
|
|
|
|
0.01 -
1.00
|
|
|
|
0.70 -
4.00
|
|
|
|
0.07 -
0.94
|
|
Dividend
yield
|
|
|
0%
|
|
|
|
0%
|
|
|
|
0%
|
|
|
|
0%
|
|
Expected
volatility
|
|
|
156.29% - 273.70%
|
|
|
|
115.46% - 239.93%
|
|
|
|
197.83% - 263.33%
|
|
|
|
279.01% - 555.60%
|
|
F-20
NOTE
10: INCOME TAXES
Deferred taxes are
provided on a liability method whereby deferred tax assets are
recognized for deductible temporary differences and operating loss
and tax credit carry-forwards and deferred tax liabilities are
recognized for taxable temporary differences. Temporary differences
are the differences between the reported amounts of assets and
liabilities and their tax bases. Deferred tax assets are reduced by
a valuation allowance when, in the opinion of management, it is
more likely than not that some portion or all of the deferred tax
assets will not be realized. Deferred tax assets and liabilities
are adjusted for the effects of changes in tax laws and rates on
the date of enactment.
Net deferred tax
assets consist of the following components as of December 31, 2016
and 2015:
|
December
31, 2016
|
December
31, 2015
|
Deferred tax
assets:
|
|
|
Net operating loss
carryover
|
$8,854,900
|
$8,007,900
|
Depreciation
|
-
|
247,900
|
Related party
accrual
|
179,400
|
113,400
|
Capital Loss
Carryover
|
5,500
|
5,500
|
Deferred tax
liabilities
|
|
|
Depreciation
|
(197,200)
|
-
|
Valuation
allowance
|
(8,842,600)
|
(8,374,700)
|
Net deferred tax
asset
|
$-
|
$-
|
Net deferred tax
asset$
|
-
|
$-
|
The income tax
provision differs from the amount of income tax determined by
applying the U.S. Federal income tax rate to pretax income from
continuing operations for the years ended December 31, 2016 and
2015 due to the following:
|
December
31, 2016
|
December
31, 2015
|
Book income
(loss)
|
$(3,350,700)
|
$2,119,100
|
Grant
income
|
(7,100)
|
(7,100)
|
Depreciation
|
(25,300)
|
(41,500)
|
Intangible asset
impairment
|
12,100
|
-
|
Related party
accrual
|
65,900
|
(516,100)
|
Meals and
entertainment
|
1,600
|
1,600
|
Stock for
services
|
341,300
|
113,900
|
Options
expense
|
229,600
|
9,700
|
Non-cash interest
expense
|
1,976,300
|
581,500
|
Other
non-deductable expenses
|
(90,600)
|
(3,112,100)
|
Valuation
allowance
|
846,900
|
851,000
|
Income tax
expense
|
$-
|
$-
|
At December 31,
2016, the Company had net operating loss carryforwards of
approximately $26,043,700 that may be offset against future taxable
income from the year 2017 through 2036.
Due to the change
in ownership provisions of the Tax Reform Act of 1986, net
operating loss carryforwards for Federal income tax reporting
purposes are subject to annual limitations. Should a
change in ownership occur, net operating loss carryforwards may be
limited as to use in future years.
F-21
Topic 740 provides
guidance on the accounting for uncertainty in income taxes
recognized in a company’s financial statements. Topic 740
requires a company to determine whether it is more likely than not
that a tax position will be sustained upon examination based upon
the technical merits of the position. If the more-likely-than-not
threshold is met, a company must measure the tax position to
determine the amount to recognize in the financial statements. At
the adoption date of January 1, 2007, the Company had no
unrecognized tax benefit, which would affect the effective tax rate
if recognized.
The Company
includes interest and penalties arising from the underpayment of
income taxes in the statements of operations in the provision for
income taxes. As of December 31, 2016, the Company had no accrued
interest or penalties related to uncertain tax
positions.
The Company files
income tax returns in the U.S. federal jurisdiction. The Company is
located in the state of Washington and Washington state does not
require the filing of income taxes. With few exceptions, the
Company is no longer subject to U.S. federal, state and local, or
non-U.S. income tax examinations by tax authorities for years
before 2013.
NOTE
11: STOCKHOLDERS’ EQUITY
As of December 31,
2016 and 2015, the Company has 20,000,000 shares of Series A
Preferred authorized with a par value of $0.001. The
Company’s Board of Directors is authorized to provide for the
issuance of shares of preferred stock in one or more series, to
establish the number of shares in each series, and to determine the
designations, preferences and rights through a resolution of the
Board of Directors.
Effective June of
2015, the Board of Directors designated the Series A Preferred as a
new series of preferred stock. As of December 31, 2016 and 2015,
the Company has 5,000,000 shares of Series A Preferred authorized,
with a par value of $0.001, and as of December 31, 2016 and 2015,
the Company has 3,773,592 and 1,627,000 shares issued and
outstanding, respectively. Each Series A Preferred share is
convertible into shares of the Company’s common stock at a
conversion price of $0.50 per share, subject to adjustment. Each
holder of Series A Preferred is entitled to the equivalent of five
votes for every conversion share, where the conversion shares are
the number of common stock the Series A Preferred would be
convertible into. The holders of the Series A Preferred have a
liquidation preference equal to $5.00 per share.
The Company has
2,000,000,000 shares of common stock authorized, with a par value
of $0.001, and as of December 31, 2016 and 2015, the Company has
31,743,797 and 19,969,341 shares issued and outstanding,
respectively.
As of December 31,
2015, there was an insufficient amount of the Company’s
authorized common stock to satisfy the potential number of shares
that would be required to satisfy the outstanding options, warrants
and convertible debt into common stock. As a result, the Company
recorded a liability in the amount of $852,091, offset by $852,091
of equity for the year ending December 31, 2015. Effective October
2016, the Company filed a Certificate of Amendment to perform a
1:100 reverse stock split which eliminated the shortage of
sufficient authorized common shares. Additionally, the Company
removed the $852,091 liability for lack of authorized shares and
increased paid in capital. The Company’s financial statements
have been retroactively adjusted for all periods presented to
reflect the reverse stock split.
Common
Stock Issued for the Exercise of Options and Warrants
During 2015, the
Company issued 1,995,000 shares of common stock for cashless
warrants exercise.
During 2016, the
Company issued 30,644 shares of common stock for cashless warrants
exercise.
F-22
Common
Stock Issued for Loan Fees on Convertible Debt
During the year
ending December 31, 2016, the Company did not issue any common
stock for loan fees.
During the year
ending December 31, 2015, the Company issued 43,326 shares of
common stock for loan fees when entering into related party
convertible notes. The shares were valued at $6,387, of which
$4,896 was allocated to a debt discount (see Note 6) and $1,491 was
recorded as interest expense.
Common
Stock Issued for Settlement and Conversion of Debt
During 2016, the
Company issued 563,523 shares of common stock in conjunction with
the settlement of convertible debt that was paid in cash. The
shares were valued at $70,863 and were recognized as a loss on the
settlement of debt.
During 2015, the
Company issued 920,516 shares of common stock valued at $109,812 in
exchange for convertible debt raised in 2014 resulting in a
reduction in debt of $31,721, a reduction in derivative liability
of $79,044, with an offset of $3,035 to debt discount and a $2,083
gain on extinguishment of debt.
Common
Stock Issued for Conversion of Preferred Stock
During 2016, the
Company issued 11,180,289 shares of common stock valued at
$1,590,801 in exchange for 1,118,024 shares of Series A Preferred
valued at $4,828,204, resulting in an increase in retained earnings
of $3,237,403.
Common Stock Options
The following
schedule summarizes the changes in the Company’s stock
options:
|
|
|
Weighted
|
|
Weighted
|
|
Options Outstanding
|
Average
|
|
Average
|
|
|
Number
|
Exercise
|
Remaining
|
Aggregate
|
Exercise
|
|
Of
|
Price
|
Contractual
|
Intrinsic
|
Price
|
|
Shares
|
Per
Share
|
Life
|
Value
|
Per
Share
|
|
|
|
|
|
|
Balance at December
31, 2014
|
87,850
|
$9.00-15.00
|
3.42
years
|
$-
|
$14.00
|
|
|
|
|
|
|
Options
granted
|
-
|
$-
|
-
|
|
$-
|
Options
exercised
|
-
|
$-
|
-
|
|
$-
|
Options
expired
|
(36,500)
|
$9.00-21.00
|
-
|
|
$12.00
|
|
|
|
|
|
|
Balance at December
31, 2015
|
51,350
|
$12.00-15.00
|
7.12
years
|
$-
|
$15.00
|
|
|
|
|
|
|
Options
granted
|
2,370,000
|
$0.50-1.00
|
-
|
|
$0.62
|
Options
exercised
|
-
|
$-
|
-
|
|
$-
|
Options
expired
|
(18,850)
|
$0.12-0.15
|
-
|
|
$14.84
|
|
|
|
|
|
|
Balance at December
31, 2016
|
2,402,500
|
$0.50-15
|
4.05
years
|
$-
|
$0.81
|
|
|
|
|
|
|
Exercisable at
December 31, 2016
|
1,939,062
|
$0.50-15
|
3.95
years
|
$-
|
$0.88
|
During the year
ending December 31, 2016 and 2015, the Company recognized $675,324
and $80,635, respectively, worth of stock based compensation
related to the vesting of it stock options.
F-23
Common
Stock Warrants
The following
schedule summarizes the changes in the Company’s common stock
warrants:
|
|
|
Weighted
|
|
Weighted
|
|
Warrants Outstanding
|
Average
|
|
Average
|
|
|
Number
|
Exercise
|
Remaining
|
Aggregate
|
Exercise
|
|
Of
|
Price
|
Contractual
|
Intrinsic
|
Price
Per
|
|
Shares
|
Per
Share
|
Life
|
Value
|
Share
|
|
|
|
|
|
|
Balance at December
31, 2014
|
23,107,701
|
$0.01-25
|
2.86
years
|
$-
|
$1
|
|
|
|
|
|
|
Warrants
granted
|
312,500
|
$0.10-0.15
|
2.94
years
|
|
$0.13
|
Warrants
exercised
|
(2,856,041)
|
$0.30
|
-
|
|
$0.30
|
Warrants adjusted
(1)
|
(13,601,951)
|
$0.10-0.15
|
-
|
|
0.01
|
Warrants
expired/cancelled
|
(158,706)
|
$6.00-25.00
|
-
|
|
$8.76
|
|
|
|
|
|
|
Balance at December
31, 2015
|
6,803,503
|
$0.1-10
|
1.90
years
|
$2,052,699
|
$0.81
|
|
|
|
|
|
|
Warrants
granted
|
233,334
|
$0.40
|
1.71
years
|
|
$0.34
|
Warrants
exercised
|
(202,500)
|
$0.10
|
-
|
|
$0.10
|
Warrants
expired/cancelled
|
(3,254,832)
|
$0.01-6.00
|
-
|
|
$0.13
|
|
|
|
|
|
|
Balance at December
31, 2016
|
3,579,505
|
$0.01-10
|
0.52
years
|
$749
|
$4.45
|
|
|
|
|
|
|
Exercisable at
December 31, 2016
|
3,579,505
|
$0.01-10
|
0.52
years
|
$749
|
$4.45
|
(1)
Based upon Delaware
law and on the terms and conditions set forth in the applicable
warrant agreement, any adjustments to the warrants were limited to
a floor price of $0.001. Pursuant to the defective warrant exercise
notice using an exercise price below $0.001, the Company issued at
total of 1,473,777 shares of common stock to the warrant holders,
which the Company believes are voidable, and also recorded
16,009,450 warrants outstanding to the holder on the
Company’s financial statements for the year ended December
31, 2014, and for the periods ending March 31 and June 30,
2015. Management believes that the warrants were recorded in
error during the periods presented, and has recorded the revised
number of warrants outstanding at September 30, 2015 at 2,407,500,
which reflects the number of shares of common stock purchase
warrants outstanding and exercisable under the terms of the
warrants at an exercise price of $0.001 per share. This net
adjustment of 13,601,951 warrants has been reflected in the
schedule for the twelve months ending December 31, 2015. The
Company reached a Settlement Agreement in 2016 with this warrant
holder to cancel all the remaining 2,407,500 warrants in exchange
for 50,000 shares of Series A Preferred.
During the year
ending December 31, 2016 and 2015, the Company recognized $595,175
and $0, respectively, worth of expense related to warrants granted
for services.
Preferred
Stock Issued for Cash
During 2016, the
Company issued 46,666 shares of Series A Preferred for $70,000
cash.
Preferred
Stock Issued for Exercise of Warrants
During 2016, the
Company issued 250,000 shares of Series A Preferred for $250 for
the exercise of warrants.
F-24
Preferred
Stock Issued for Warrants Surrendered
During 2016, the
Company issued 62,854 shares of Series A Preferred, representing
$407,973, in exchange for the surrender of 2,407,500 warrants. This
resulted in the Company writing off $1,179,710 worth of derivative
liabilities and recognizing a gain on debt extinguishment of
$771,737.
Preferred
Stock Issued for Services
During 2016, the
Company issued 218,000 shares of its Series A Preferred,
representing $942,644, for services valued at $949,661, therefore
recognizing $7,018 of a gain on settlement of debt. During 2016,
the Company issued 10,000 shares of its Series A Preferred to its
CFO, representing $54,152, for services (see Note 6).
During 2015, the
Company issued 100,000 shares of its Series A Preferred,
representing $334,880, for services.
Preferred
Stock Issued for Loan Fees
During 2016, the
Company issued 30,000 shares of its Series A Preferred, valued at
$162,456, as a finders fee and issued 37,906 shares of its Series A
Preferred, valued at $29,156 (see Note 6), as loan fees on related
party convertible notes. The Company also issued 347,400 shares of
its Series A Preferred, valued at $363,807, as loan fees on
convertible notes recorded as debt discount (see Note 8), and
issued 47,840 shares of its Series A Preferred, valued at $39,904,
as loan fees on convertible notes recorded as derivative
liabilities.
During 2015, the
Company issued 133,833 shares of its Series A Preferred, valued at
$527,325, as loan fees on convertible notes and issued 3,440 shares
of its Series A Preferred, valued at $17,401 (see Note 6), as loan
fees on related party convertible notes.
Preferred
Stock Issued for Debt Extinguishment
During 2016, the
Company issued 215,961 shares of Series A Preferred, valued at
$1,401,760, in exchange for $1,197,950 of related party debt, and
$59,671 of accrued interest (see Note 6). This resulted in the
Company recognizing $144,139 as a loss on debt
extinguishment.
During 2016, the
Company issued 473,830 shares of Series A Preferred, valued at
$2,330,876, in exchange for $473,613 of related party convertible
debt, and $0 of accrued interest (see Note 6). This resulted in the
Company writing off $2,330,154 in derivative liabilities, $448,613
in debt discounts, and recognizing $24,278 as a gain on debt
extinguishment.
During 2016, the
Company issued 1,460,600 shares of Series A Preferred, valued at
$8,552,746 in exchange for $1,444,950 of convertible debt, and
$50,711 of accrued interest (see Note 8). This resulted in the
Company writing off $8,138,070 in derivative liabilities, $814,625
in debt discounts, and recognizing $266,358 as a gain on debt
extinguishment.
In September 2015,
the Company issued 148,310 shares of Series A Preferred in exchange
for $1,414,100 of related party debt plus $810,538 of accrued
interest and 207,620 shares of Series A preferred stock in exchange
for $2,224,466 of related party debt plus $889,838 of accrued
interest, to the major shareholder and director of the Company (see
Note 6).
In September 2015,
the Company issued 43,000 shares of Series A Preferred in exchange
for $43,000 of related party convertible debt raised during 2015
(see Note 6).
In November and
December 2015, the Company issued 99,000 shares of Series A
Preferred in exchange for $22,700 of convertible debt, $9,812 of
accrued interest, and extension of a due date for a payment on a
debt settled. In September 2015 the Company issued 552,000 shares
of Series A Preferred in exchange for $552,000 of convertible debt
raised during 2015. In October 2015 the Company issued 10,000
shares of Series A Preferred in exchange for $10,000 of convertible
debt raised during 2015 (see Note 8).
F-25
Preferred
Stock Issued for Accounts Payable and Accrued
Liabilities
In December 2015,
the Company issued 100,000 and 75,000 shares of Series A Preferred
to the CEO and CFO, in exchange for $150,000 and $112,500,
respectively, of accrued payroll (see Note 6). In December 2015,
the Company issued 246,797 shares of Series A Preferred in exchange
for $370,197 of accounts payable.
NOTE
12: CONCENTRATIONS OF CREDIT AND OTHER RISKS
Accounts
Receivable
The Company had one
customer that represented 100% of the Company’s total
revenues for each of the years ended December 31, 2016 and 2015.
The customer that represented 100% of the Company’s total
revenue for the years ended December 31, 2016 and 2015, and
accounted for 100% of the consulting revenue for that year. The
Company had no net accounts receivable balance at December 31, 2016
and 2015.
The loss of a
significant customer representing the percentage of total revenue
as represented for the years ended December 31, 2016 and 2015 would
have a temporary adverse effect on the Company’s revenue,
which would continue until the Company located new customers to
replace them.
The Company
routinely assesses the financial strength of its customers and
provides an allowance for doubtful accounts as necessary. As of
December 31, 2016 and 2015, the Company had no allowance or bad
debt expense recorded.
NOTE
13: SUPPLEMENTAL CASH FLOW INFORMATION
During the year
ended December 31, 2016, the Company had the following non-cash
investing and financing activities:
-
Issued 30,644
shares of common stock valued at $0 for the issuance of cashless
warrants.
-
Decreased related
party notes by $1,197,950, decrease related party convertible notes
by $473,613, offset by a decrease $448,613 in debt discount
decreased convertible notes payable by $1,444,950, offset by a
decrease $814,624 in debt discount, decreased accrued interest by
$110,382, decreased derivative liabilities by $10,468,224, and
increased Series A Preferred by $12,431,882 due to 2,150,391 shares
issued in conjunction with the settlement of convertible
notes.
-
Increased
convertible notes payable and decreased accrued interest by
$455,150 for the reclassification of accrued interest to
principal.
-
Issued 62,854
shares of Series A Preferred, valued at $407,973, which decreased
derivative liabilities by $1,179,710 and for which a gain on debt
extinguishment was recorded for $771,737.
-
Increased
derivative liabilities for $1,283,448 to record a debt discount on
related party convertible notes of $473,613 and a debt discount on
convertible notes of $809,835.
-
Increased paid in
capital and decreased liability for lack of authorized shares for
$852,092.
-
Increased
convertible notes payable and decreased loan from shareholder by
$127,533 to roll proceeds from shareholder advances to a formal
convertible note payable.
-
Issued 433,146
shares of Series A Preferred, valued at $432,866, for loan fees
that increased the convertible note debt discount by $363,807 and
increased derivative liabilities by $69,059.
-
Issued 11,180,289
shares of common stock valued at $1,590,801 in exchange for
1,118,024 shares of Series A Preferred valued at $4,828,204,
resulting in an increase in retained earnings of
$3,237,403.
F-26
During the year
ended December 31, 2015, the Company had the following non-cash
investing and financing activities:
-
Issued 1,995,000
shares of common stock valued at $0 for the issuance of cashless
warrants.
-
Issued 43,326
shares of common stock as loan fees on convertible
debt.
-
Issued 108,833
shares of preferred stock as loan fees on convertible
debt.
-
Issued 920,516
shares of common stock for an extinguishment of $31,721 worth of
principal on convertible notes payable $0 worth of accrued
interest, $79,044 worth of derivative liabilities and $3,035 worth
of debt discount.
-
Issued 74,000
shares of preferred stock for an extinguishment of $22,700 worth of
principal on convertible notes payable $0 worth of accrued
interest, $0 worth of derivative liabilities and $0 worth of debt
discount.
-
Issued 960,929
shares of preferred stock valued at $2,201,963 in exchange for
$4,243,566 of notes.
-
Issued 421,797
shares of preferred stock valued at $1,358,726 in exchange for
$370,197 of accounts payable and $262,500 of accrued
payroll.
-
Issued 25,000
shares of preferred stock as loan extension fees.
NOTE 14: SUBSEQUENT EVENTS
In January,
February and through March 6, 2017, the Company issued 5,517,900
shares of common stock for 531,790 shares of Series A
Preferred.
In February 2017,
the Company issued 280,000 shares of common stock shares in
exchange for $140,000 of accounts payable.
In March 2017, the
Company received $25,000 as a shareholder loan.
The
Company has evaluated subsequent events pursuant to ASC Topic 855
and has determined that there are no additional subsequent events
to disclose.
F-27
PROSPECTUS
$
10,000,000
Common Stock
Warrants
[________________], 2017
All dealers that buy, sell or trade the common stock
identified herein may be required to deliver a prospectus,
regardless of whether they are participating in this offering. This
is in addition to the dealers’ obligation to deliver a
prospectus when acting as underwriters and with respect to their
unsold allotments or subscriptions.
PART II
INFORMATION NOT REQUIRED IN PROSPECTUS
Item 13. Other Expenses of Issuance and
Distribution
The following table presents the costs and
expenses in connection with the issuance and distribution of the
securities to be registered, other than commissions payable by us
in connection with the sale of common stock being registered.
Except as otherwise noted, we will pay all of these amounts. All
amounts are estimates except the Securities and Exchange Commission
(“SEC”) registration fee and the Financial
Industry Regulatory Authority (“FINRA”) registration fee.
SEC registration
fee
|
$1,159.00
|
Accounting fees and
expenses
|
$10,000.00
|
Legal fees and
expenses
|
$25,000.00
|
Blue Sky filing
fees
|
$10,000.00
|
Miscellaneous fees
and expenses
|
$10,000.00
|
Total
|
$56,159.00
|
Item 14. Indemnification of Directors and
Officers
Insofar as indemnification for liabilities arising
under the Securities Act of 1933 (the “Securities
Act”) may be permitted to
our directors, officers and controlling persons pursuant to the
foregoing provisions, or otherwise, we have been advised that in
the opinion of the SEC such indemnification is against public
policy as expressed in the Securities Act and is, therefore,
unenforceable.
No
director of Innovus will have personal liability to us or any of
our stockholders for monetary damages for breach of fiduciary duty
as a director involving any act or omission of any such director
since provisions have been made in our Articles of Incorporation
limiting such liability. The foregoing provisions shall not
eliminate or limit the liability of a director for:
●
any
breach of the director’s duty of loyalty to us or our
stockholders
●
acts
or omissions not in good faith or, which involve intentional
misconduct or a knowing violation of law
●
or
under applicable Sections of the Delaware Revised
Statutes
●
the
payment of dividends in violation of Section 78.300 of the Delaware
Revised Statutes, or
●
for
any transaction from which the director derived an improper
personal benefit.
The
Bylaws provide for indemnification of our directors, officers and
employees in most cases for any liability suffered by them or
arising out of their activities as directors, officers and
employees if they were not engaged in willful misfeasance or
malfeasance in the performance of his or her duties; provided that
in the event of a settlement the indemnification will apply only
when the board of directors approves such settlement and
reimbursement as being for our best interests. The Bylaws,
therefore, limit the liability of directors to the maximum extent
permitted by Delaware law (Section 78.751).
Our
officers and directors are accountable to us as fiduciaries, which
means, they are required to exercise good faith and fairness in all
dealings affecting Innovus. In the event that a stockholder
believes the officers and/or directors have violated their
fiduciary duties, the stockholder may, subject to applicable rules
of civil procedure, be able to bring a class action or derivative
suit to enforce the stockholder’s rights, including rights
under certain federal and state securities laws and regulations to
recover damages from and require an accounting by management.
Stockholders, who have suffered losses in connection with the
purchase or sale of their interest in Innovus in connection with
such sale or purchase, including the misapplication by any such
officer or director of the proceeds from the sale of these
securities, may be able to recover such losses from
us.
II-1
Item 15. Recent Sales of Unregistered
Securities
We have issued the following securities
since January 1, 2014 that were
not registered under the Securities Act:
Common Stock Issued for the Exercise of Options and
Warrants
In
April 2014, the Company issued 130,435 shares of its common stock
in exchange for the cancellation of certain warrants attached to
the convertible notes received in July 2012.
During
2014, the Company issued 362,040,378 shares of common stock in
connection with the cashless exercise of certain
warrants.
During
2015, the Company issued 1,995,000 shares of common stock in
connection with the cashless exercise of certain
warrants.
During
2016, the Company issued 30,644 shares of common stock in
connection with the cashless exercise of certain
warrants.
Common Stock Issued for Loan Fees on Convertible Debt
During
the year ending December 31, 2015, the Company issued 43,326 shares
of common stock for loan fees when entering into related party
convertible notes. The shares were valued at $6,387, of which
$4,896 was allocated to a debt discount (see Note 6) and $1,491 was
recorded as interest expense.
During
the year ending December 31, 2014, the Company issued 2,904,160
shares of common stock for loan fees when entering into related
party convertible notes. The shares were valued at
$3,891.
During
the year ending December 31, 2014, the Company issued 1,232,609
shares of common stock for loan fees when entering into related
party convertible notes. The shares were valued at
$240,243.
Common Stock Issued for Services and Prepaid Services
During
2014, the Company issued 471,250 shares of its common stock,
representing $23,800, to a consultant in consideration for services
rendered.
Common Stock Issued for Settlement and Conversion of
Debt
During
2016, the Company issued 563,523 shares of common stock in
connection with the settlement of convertible debt that was paid in
cash. The shares were valued at $70,863 and were recognized as a
loss on the settlement of debt.
During
2015, the Company issued 920,516 shares of common stock valued at
$109,812 in exchange for convertible debt issued in 2014, resulting
in a reduction in debt of $31,721, a reduction in derivative
liability of $79,044, with an offset of $3,035 to debt discount and
a $2,083 gain on extinguishment of debt.
On May 15, 2014, the Company entered into an agreement with
Battelle Memorial Institute, an Ohio nonprofit corporation
(“Battelle”), pursuant to which the Company issued to
Battelle (i) a 10% convertible debenture in the principal amount of
$350,000 (the “Debenture”), (ii) a warrant (the
“Warrant”) exercisable for shares of common stock of
the Company, and (iii) 532,609 shares of common stock in
satisfaction of a promissory note issued by the Company to Battelle
on May 1, 2013 in the principal amount of $349,913.41 as payment
for research services performed by Battelle for the Company. The
Debenture was scheduled to mature on May 15, 2015 and on June 6,
2014, Battelle converted the Debenture into Common Stock for a
total issuance of 16,530,974 shares of Common
Stock.
During 2014, the holders of the certain convertible debt
instruments exercised their conversion rights and converted the
outstanding principal and accrued interest balances, respectively,
into 1,204,092,687 shares of the Company’s common stock. The
fair market value of the shares issued was determined based on the
market value of the shares on the date of conversion. The total
fair market value of the shares issued was $3,043,368 and a debt
discount of $418,896 was
written off to equity for the unamortized balance of the debt
converted. Additionally, the derivative liability for the debt
converted of $1,702,018 was written off, resulting in a loss on
extinguishment of debt of $126,123.
II-2
Common Stock Issued for Conversion of Preferred Stock
During
2016, the Company issued 11,180,289 shares of common stock valued
at $1,590,801 in exchange for 1,118,024 shares of Series A
Preferred valued at $4,828,204, resulting in an increase in
retained earnings of $3,237,403.
During
the year ending December 31, 2016 and 2015, the Company recognized
$595,175 and $0, respectively, worth of expense related to warrants
granted in consideration for services rendered.
Preferred Stock Issued for Cash
During
2016, the Company issued 46,666 shares of Series A Preferred for
$70,000 cash.
Preferred Stock Issued for Exercise of Warrants
During
2016, the Company issued 250,000 shares of Series A Preferred for
$250 for the exercise of warrants.
Preferred Stock Issued for Warrants Surrendered
During
2016, the Company issued 62,854 shares of Series A Preferred,
representing $407,973, in exchange for the surrender of 2,407,500
warrants. This resulted in the Company writing off $1,179,710 worth
of derivative liabilities and recognizing a gain on debt
extinguishment of $771,737.
Preferred Stock Issued for Services
During
2016, the Company issued 218,000 shares of its Series A Preferred,
representing $942,644, for services rendered valued at $949,661,
therefore recognizing $7,018 of a gain on settlement of debt.
During 2016, the Company issued 10,000 shares of its Series A
Preferred to its CFO, representing $54,152, for services (see Note
6).
During
2015, the Company issued 100,000 shares of its Series A Preferred,
representing $334,880, in consideration for services
rendered.
Preferred Stock Issued for Loan Fees
During
2016, the Company issued 30,000 shares of its Series A Preferred,
valued at $162,456, as a finders fee and issued 37,906 shares of
its Series A Preferred, valued at $29,156 (see Note 6), as loan
fees on related party convertible notes. The Company also issued
347,400 shares of its Series A Preferred, valued at $363,807, as
loan fees on convertible notes recorded as debt discount (see Note
8), and issued 47,840 shares of its Series A Preferred, valued at
$39,904, as loan fees on convertible notes recorded as derivative
liabilities.
During
2015, the Company issued 133,833 shares of its Series A Preferred,
valued at $527,325, as loan fees on convertible notes and issued
3,440 shares of its Series A Preferred, valued at $17,401 (see Note
6), as loan fees on related party convertible notes.
Preferred Stock Issued for Debt Extinguishment
During
2016, the Company issued 215,961 shares of Series A Preferred,
valued at $1,401,760, in exchange for $1,197,950 of related party
debt, and $59,671 of accrued interest (see Note 6). This resulted
in the Company recognizing $144,139 as a loss on debt
extinguishment.
During
2016, the Company issued 473,830 shares of Series A Preferred,
valued at $2,330,876, in exchange for $473,613 of related party
convertible debt, and $0 of accrued interest (see Note 6). This
resulted in the Company writing off $2,330,154 in derivative
liabilities, $448,613 in debt discounts, and recognizing $24,278 as
a gain on debt extinguishment.
During
2016, the Company issued 1,460,600 shares of Series A Preferred,
valued at $8,552,746 in exchange for $1,444,950 of convertible
debt, and $50,711 of accrued interest (see Note 8). This resulted
in the Company writing off $8,138,070 in
derivative liabilities, $814,625 in debt discounts, and recognizing
$266,358 as a gain on debt extinguishment.
II-3
In
September 2015, the Company issued 148,310 shares of Series A
Preferred in exchange for $1,414,100 of related party debt plus
$810,538 of accrued interest and 207,620 shares of Series A
preferred stock in exchange for $2,224,466 of related party debt
plus $889,838 of accrued interest, to the major shareholder and
director of the Company (see Note 6).
In
September 2015, the Company issued 43,000 shares of Series A
Preferred in exchange for $43,000 of related party convertible debt
raised during 2015 (see Note 6).
In
November and December 2015, the Company issued 99,000 shares of
Series A Preferred in exchange for $22,700 of convertible debt,
$9,812 of accrued interest, and extension of a due date for a
payment on a debt settled. In September 2015 the Company issued
552,000 shares of Series A Preferred in exchange for $552,000 of
convertible debt issued during 2015. In October 2015 the Company
issued 10,000 shares of Series A Preferred in exchange for $10,000
of convertible debt issued during 2015 (see Note
8).
Preferred Stock Issued for Accounts Payable and Accrued
Liabilities
In
December 2015, the Company issued 100,000 and 75,000 shares of
Series A Preferred to the Company’s CEO and CFO, in exchange
for $150,000 and $112,500, respectively, of accrued payroll (see
Note 6). In December 2015, the Company issued 246,797 shares of
Series A Preferred in exchange for $370,197 of accounts
payable.
Preferred Stock Warrants
During
October 2015, 250,000 warrants to purchase the Company’s
Series A Preferred with an exercise price of $0.001 were issued as
part of a consulting services agreement.
Common Stock Warrants
During the year ended December 31, 2014, the Company granted
50,000,000 warrants to a convertible note holder due to the note
holders’ inability to exercise its conversion option on an
outstanding note due to the lack of authorized shares. The warrants
have an exercise price of $0.001. Warrants exercisable for
10,000,000 shares of common stock expired on September 11, 2016 and
warrants exercisable for 40,000,000 shares of common stock expire
December 29, 2019.
During the year end December 31, 2014, the Company issued 375,000
warrants to purchase the Company’s common stock in
conjunction with convertible debt (see Note 10: convertible Notes
Payable), which resulted in a debt discount derivative liability
(see Note 11: Derivative Liability) and loss on derivative being
recorded upon issuance. The warrants have an exercise price of
$0.046 and expire July 24, 2019.
During the year ended December 31, 2014, the Company granted
warrants to purchase the Company’s common stock in
conjunction with a $350,000 convertible note. In addition to the
warrants 532,009 shares of common stock were also issued with this
convertible note. The number of exercise shares that the holder may
purchase by exercising this warrant is equal to the quotient
obtained by dividing the related convertible debenture original
principal of $350,000 by the warrant exercise price. The exercise
price is the lesser of the market value of these shares, which is
defined as the mean market closing price over 10 trading days
immediately prior to the notice date of exercise and $0.046. The
value of the $350,000 debt plus the fair value of the warrants and
the fair value of the common stock at the date of agreement was
prorated to arrive at the allocation of the original $350,000 debt
and the value of the warrants plus common stock. The computation
resulted in allocation of $127,925 to the warrants and $10,619 to
the common stock shares of the total value of the warrants and
common stock of $128,543 was recorded as a debt discount and
amortized to interest over the life of the note at December 31,
2014, the note was converted in full into shares of common stock
and there was no exercise of the warrants. Following the terms of
the agreement for exercise number of shares, the Company calculated
318,181,518 warrants outstanding. This number will fluctuate at
each reporting period due to the fluctuating exercise of shares.
These warrants expire May 15, 2017.
II-4
During the year ended December 31, 2014, the Company granted
warrants to purchase the Company’s common stock in
conjunction with two convertible notes with the same note holder.
With the first convertible note, the number of warrant shares is
equal to $85,000 divided by the market price, which is defined as
the higher of the closing price of the common stock on the issuance
date and the VWAP (volume weighted average price) of common stock
for the two trading days prior to the exercizes. Following these
terms a total of 68,000,000 warrants were outstand at December 31,
2014. These warrants expire March 31, 2019 and have and exercise
price of $0.11. For the second note, the number of shares is
calculated the same as the first except for the number of warrant
shares is found by dividing $27,500 by the previously defined
market price. Following the terms a total of 22,000,000 warrants
were outstand at December 31, 2014. These warrants expire June 30,
2019 and have and exercise price of $0.11.
During April 2014, in accordance with the December 31,
2012 convertible debt instrument, which included Additional
Investment Rights that were exercised May 15, 2013, the court
ordered that 4,000,000 warrants and 1,183,333 warrants to purchase
the Company’s common stock that were originally issued with
an exercise price of $0.06 be modified to be
18,260,469 warrants with an exercise price of
$0.046 The Company reported this change as a
cancellation of the original warrants and an issuance of the new
warrants. Additionally, the April 2014 court order
required the exercise of a total of 426,019 warrants to purchase
common related to prior year warrant exercises.
During August, 2014, 1,401,570 warrants to purchase the
Company’s common stock with an exercise price of $0.06 which
were issued as part the December 31, 2012 convertible debt
instrument, which included Additional Investment Rights that were
exercised May 15, 2013 were exercised in a cashless
exercise. In accordance with the agreement, those
warrants were modified to be 11,111,111 warrants with an exercise
price of $0.0058. The Company is reporting this change
as a cancellation of the original warrants and an issuance of the
new warrants.
During August, 2014, 1,011,522 warrants to purchase the
Company’s common stock with an exercise price of $0.06 which
were issued as part the December 31, 2012 convertible debt
instrument, which included Additional Investment Rights that were
exercised May 15, 2013 were exercised in a cashless
exercise. In accordance with the agreement, those
warrants were modified to be 18,000,000 warrants with an exercise
price of $0.00475. The Company is reporting this change
as a cancellation of the original warrants and an issuance of the
new warrants.
During September, 2014, 1,576,087 warrants to purchase the
Company’s common stock with an exercise price of $0.06 which
were issued as part the December 31, 2012 convertible debt
instrument, which included Additional Investment Rights that were
exercised May 15, 2013 were exercised in a cashless
exercise. In accordance with the agreement, those
warrants were modified to be 25,000,000 warrants with an exercise
price of $0.0035. The Company is reporting this change
as a cancellation of the original warrants and an issuance of the
new warrants.
During October, 2014, 920,652 warrants to purchase the
Company’s common stock with an exercise price of $0.06 which
were issued as part the December 31, 2012 convertible debt
instrument, which included Additional Investment Rights that were
exercised May 15, 2013 were exercised in a cashless
exercise. In accordance with the agreement, those
warrants were modified to be 35,000,000 warrants with an exercise
price of $0.00121. The Company is reporting this change
as a cancellation of the original warrants and an issuance of the
new warrants.
During November, 2014, in accordance with the December 31, 2012
convertible debt instrument, which included Additional Investment
Rights that were exercised May 15, 2013, the court ordered that all
prior warrants issued to the warrant holder be modified to be a
total of 501,059,809 warrants with an exercise price of
$0.03317 During December 2014, the warrant holder
exercised a total of 215,455,718 for cashless
exercise.
During April 2014, in accordance with the December 31, 2012
convertible debt instrument, which included Additional Investment
Rights that were exercised May 15, 2013, the court ordered that a
separate warrant holder’s 550,000 warrants to purchase the
Company’s common stock that were originally issued with an
exercise price of $0.06 be modified to be
1,793,478 warrants with an exercise price of
$0.046 The Company reported this change as a
cancellation of the original warrants and an issuance of the new
warrants.
During August, 2014, 1,793,478 warrants to purchase the
Company’s common stock with an exercise price of $0.06 which
were issued as part the December 31, 2012 convertible debt
instrument, which included Additional Investment Rights that were
exercised May 15, 2013 were exercised in a cashless
exercise. In accordance with the agreement, those
warrants were modified to be 14,218,007 warrants with an exercise
price of $0.0058. The Company reported
this
change as a cancellation of the original warrants and an issuance
of the new warrants.
II-5
During April 2014, in accordance with the December 31, 2012
convertible debt instrument, which included Additional Investment
Rights that were exercised May 15, 2013, a third warrant
holder’s 1,500,000 warrants and 600,000 warrants to purchase
the Company’s common stock that were originally issued with
an exercise price of $0.15 be modified to be 3,750,000 warrants and
1,500,000 respectively, both with an exercise price of
$0.06. The Company reported this change as a
cancellation of the original warrants and an issuance of the new
warrants.
During August, 2014, 742,500 warrants to purchase the
Company’s common stock with an exercise price of $0.06 which
were issued as part the December 31, 2012 convertible debt
instrument, which included Additional Investment Rights that were
exercised May 15, 2013 were exercised in a cashless
exercise. In accordance with the agreement, those
warrants were modified to be 18,000,000 warrants with an exercise
price of $0.002475. The Company reported this change as
a cancellation of the original warrants and an issuance of the new
warrants.
During September, 2014, 12,000,000 warrants to purchase the
Company’s common stock with an exercise price of $0.002475
which were issued as part the December 31, 2012 convertible debt
instrument, which included Additional Investment Rights that were
exercised May 15, 2013 were exercised in a cashless
exercise. In accordance with the agreement, those
warrants were modified to be 18,000,000 warrants with an exercise
price of $0.00165. The Company reported this change as a
cancellation of the original warrants and an issuance of the new
warrants.
During November, 2014, 10,000,000 warrants to purchase the
Company’s common stock with an exercise price of $0.00165
which were issued as part the December 31, 2012 convertible debt
instrument, which included Additional Investment Rights that were
exercised May 15, 2013 were exercised in a cashless
exercise. In accordance with the agreement, those
warrants were modified to be 30,000,000 warrants with an exercise
price of $0.00055. The Company reported this change as a
cancellation of the original warrants and an issuance of the new
warrants.
During November, 2014, 64,000,000 warrants to purchase the
Company’s common stock with an exercise price of $0.00055
which were issued as part the December 31, 2012 convertible debt
instrument, which included Additional Investment Rights that were
exercised May 15, 2013 were exercised in a cashless
exercise. In accordance with the agreement, those
warrants were modified to be 64,000,000 warrants with an exercise
price of $0.00055. The Company reported this change as a
cancellation of the original warrants and an issuance of the new
warrants.
During December, 2014, 86,491,275 warrants to purchase the
Company’s common stock with an exercise price of $0.00055
which were issued as part the December 31, 2012 convertible debt
instrument, which included Additional Investment Rights that were
exercised May 15, 2013 were exercised in a cashless
exercise. In accordance with the agreement, those
warrants were modified to be 117,691,275 warrants with an exercise
price of $0.00011. The Company reported this change as a
cancellation of the original warrants and an issuance of the new
warrants.
Each of the securities were offered and sold in transactions exempt
from registration under the Securities Act, in reliance on Section
4(a)(2) thereof and Rule 506 of Regulation D thereunder and/or
Section 3(a)(9) of the Securities Act. Each of the investors
represented that it was an "accredited investor" as defined in
Regulation D under the Securities Act.
II-6
Item 16. Exhibits and Financial Statement
Schedules
(a) Exhibits. The exhibits are incorporated by
reference to the Exhibit Index attached hereto and a part hereof by
reference.
(b) Financial
Statements. See page
52 for an index of the financial statements included in the
Registration Statement.
Item 17. Undertakings
The
undersigned registrant hereby undertakes:
1.
To file, during
any period in which offers or sales are being made, a
post-effective amendment to this registration
statement:
(i)
To include any
prospectus required by section 10(a)(3) of the Securities Act of
1933;
(ii)
To reflect in the
prospectus any facts or events arising after the effective date of
the registration statement (or the most recent post-effective
amendment thereof) which, individually or in the aggregate,
represent a fundamental change in the information set forth in the
registration statement. Notwithstanding the foregoing, any increase
or decrease in volume of securities offered (if the total dollar
value of securities offered would not exceed that which was
registered) and any deviation from the low or high end of the
estimated maximum offering range may be reflected in the form of
prospectus filed with the Commission pursuant to Rule 424(b)
(Sec.230.424(b) of this chapter) if, in the aggregate, the changes
in volume and price represent no more than a 20% change in the
maximum aggregate offering price set forth in the "Calculation of
Registration Fee" table in the effective registration statement;
and
(iii)
To include any
material information with respect to the plan of distribution not
previously disclosed in the registration statement or any material
change to such information in the registration
statement.
2.
That, for the
purpose of determining any liability under the Securities Act of
1933, each such post-effective amendment shall be deemed to be a
new registration statement relating to the securities offered
therein, and the offering of such securities at that time shall be
deemed to be the initial bona fide offering thereof.
3.
To remove from
registration by means of a post-effective amendment any of the
securities being registered which remain unsold at the termination
of the offering.
4.
That, for the
purpose of determining liability under the Securities Act of 1933
to any purchaser, each prospectus filed pursuant to Rule 424(b) as
part of a registration statement relating to an offering, other
than registration statements relying on Rule 430B or other than
prospectuses filed in reliance on Rule 430A, shall be deemed to be
part of and included in the registration statement as of the date
it is first used after effectiveness. Provided, however , that no statement
made in a registration statement or prospectus that is part of the
registration statement or made in a document incorporated or deemed
incorporated by reference into the registration statement or
prospectus that is part of the registration statement will, as to a
purchaser with a time of contract of sale prior to such first use,
supersede or modify any statement that was made in the registration
statement or prospectus that was part of the registration statement
or made in any such document immediately prior to such date of
first use.
5.
That, for the
purpose of determining liability of the registrant under the
Securities Act of 1933 to any purchaser in the initial distribution
of the securities:
II-7
The undersigned registrant undertakes that in a primary offering of
securities of the undersigned registrant pursuant to this
registration statement, regardless of the underwriting method used
to sell the securities to the purchaser, if the securities are
offered or sold to such purchaser by means of any of the following
communications, the undersigned registrant will be a seller to the
purchaser and will be considered to offer or sell such securities
to such purchaser:
(i)
Any preliminary prospectus or prospectus of the undersigned
registrant relating to the offering required to be filed pursuant
to Rule 424;
(ii)
Any free writing prospectus relating to the offering prepared by or
on behalf of the undersigned registrant or used or referred to by
the undersigned registrant;
(iii)
The portion of any other free writing prospectus relating to the
offering containing material information about the undersigned
registrant or its securities provided by or on behalf of the
undersigned registrant; and
(iv)
Any other communication that is an offer in the offering made by
the undersigned registrant to the purchaser.
Insofar as indemnification for liabilities arising under the
Securities Act of 1933 may be permitted to directors, officers, and
controlling persons of the registrant pursuant to the foregoing
provisions, or otherwise, the registrant has been advised that in
the opinion of the Securities and Exchange Commission such
indemnification is against public policy as expressed in the Act
and is, therefore, unenforceable. In the event that a claim for
indemnification against such liabilities (other than the payment by
the registrant of expenses incurred or paid by a director, officer
or controlling person of the registrant in the successful defense
of any action, suit or proceeding) is asserted by such director,
officer or controlling person in connection with the securities
being registered, the registrant will, unless in the opinion of its
counsel the matter has been settled by controlling precedent,
submit to a court of appropriate jurisdiction the question whether
such indemnification by it is against public policy as expressed in
the Act and will be governed by the final adjudication of such
issue.
II-8
SIGNATURES
Pursuant to the
requirements of the Securities Act of 1933, the registrant has duly
caused this registration statement to be signed on its behalf by
the undersigned, thereunto duly authorized, in San Diego,
California, on March 9, 2017.
|
ADVANCED
MEDICAL ISOTOPE CORPORATION
|
|
|
|
|
Date:
March 9, 2017
|
By:
|
/s/ Dr.
Michael K. Korenko
|
|
Name:
|
Dr.
Michael K. Korenko
|
|
Title:
|
Interim
Chief Executive Officer and President
|
POWER
OF ATTORNEY
KNOW ALL MEN BY THESE
PRESENTS, that each person
whose signature appears below hereby constitutes and appoints Bruce
Jolliff and Michael K. Korenko, or each of them individually, his
true and lawful attorney-in-fact and agent, with full power of
substitution and re-substitution, for him and in his name, place
and stead, in any and all capacities, to sign any and all
amendments to this Registration Statement, and any additional
related registration statement filed pursuant to Rule 462(b) under
the Securities Act of 1933, as amended (including post-effective
amendments to the registration statement and any such related
registration statements), and to file the same, with all exhibits
thereto, and any other documents in connection therewith, granting
unto said attorneys-in-fact and agents full power and authority to
do and perform each and every act and thing requisite and necessary
to be done in and about the premises, as fully to all intents and
purposes as he might or could do in person, hereby ratifying and
confirming all that said attorneys-in-fact and agents, or their
substitute or substitutes, may lawfully do or cause to be done by
virtue hereof.
Pursuant to the
requirement of the Securities Act of 1933, this registration
statement has been signed by the following persons in the
capacities and on the dates indicated.
Date:
March 9, 2017
|
By:
|
/s/ Dr.
Michael K. Korenko
|
|
Name:
|
Dr.
Michael K. Korenko
|
|
Title:
|
Interim
Chief Executive Officer, President
(Principal
Executive Officer)
|
|
|
|
Date:
March 9, 2017
|
By:
|
/s/ L. Bruce
Jolliff
|
|
Name:
|
L.
Bruce Jolliff
|
|
Title:
|
Chief
Financial Officer
(Principal
Financial and Accounting Officer)
|
|
|
|
Date:
March 9, 2017
|
By:
|
/s/ Carlton M.
Cadwell
|
|
Name:
|
Carlton
M. Cadwell
|
|
Title:
|
Chairman
of the Board of Directors
|
|
|
|
Date:
March 9, 2017
|
By:
|
/s/ James C.
Katzaroff
|
|
Name:
|
James
C. Katzaroff
|
|
Title:
|
Director
|
|
|
|
Date:
March 9, 2017
|
By:
|
/s/ Thomas J.
Clement
|
|
Name:
|
Thomas
J. Clement
|
|
Title:
|
Director
|
|
|
|
II-9
EXHIBIT INDEX
Exhibit
|
|
|
Number
|
|
Description
|
3.1
|
|
Certificate
of Incorporation of Savage Mountain Sports Corporation, dated
January 11, 2000 (incorporated by reference to Exhibit 3.1 to the
Company’s Registration Statement on Form 10-12G (File No.
000-53497) filed on November 12, 2008).
|
3.2
|
|
By-Laws
(incorporated by reference to Exhibit 3.2 to the Company’s
Registration Statement on Form 10-12G (File No. 000-53497) filed on
November 12, 2008).
|
3.3
|
|
Articles
and Certificate of Merger of HHH Entertainment Inc. and Savage
Mountain Sports Corporation, dated April 3, 2000 (incorporated by
reference to Exhibit 3.3 to the Company’s Registration
Statement on Form 10-12G (File No. 000-53497) filed on November 12,
2008).
|
3.4
|
|
Articles
and Certificate of Merger of Earth Sports Products Inc. and Savage
Mountain Sports Corporation, dated May 11, 2000 (incorporated by
reference to Exhibit 3.4 to the Company’s Registration
Statement on Form 10-12G (File No. 000-53497) filed on November 12,
2008).
|
3.5
|
|
Certificate
of Amendment of Certificate of Incorporation changing the name of
the Company to Advanced Medical Isotope Corporation, dated May 23,
2006 (incorporated by reference to Exhibit 3.5 to the
Company’s Registration Statement on Form 10-12G (File No.
000-53497) filed on November 12, 2008).
|
3.6
|
|
Certificate
of Amendment of Certificate of Incorporation increasing authorized
capital dated September 26, 2006 (incorporated by reference to
Exhibit 3.6 to the Company’s Registration Statement on Form
10-12G (File No. 000-53497) filed on November 12,
2008).
|
3.7
|
|
Certificate
of Amendment to the Certificate of Incorporation increasing
authorized common stock and authorizing preferred stock, dated May
18, 2011 (incorporated by reference to Exhibit 3.1 to the
Company’s Current Report on Form 8-K filed on May 18,
2011).
|
3.8
|
|
Certificate
of Amendment to the Certificate of Incorporation authorizing a
series of Preferred Stock to be named “Series A Convertible
Preferred Stock”, consisting of 2,500,000 shares, which
series shall have specific designations, powers, preferences and
relative and other special rights, qualifications, limitations and
restrictions as outlined in the Certificate of Designations, filed
June 30, 2015 (incorporated by reference to Exhibit 4.1 to the
Company’s Current Report on Form 8-K filed July 8,
2015).
|
3.9
|
|
Certificate
of Amendment to the Certificate of Incorporation increasing the
authorized series of “Series A Convertible Preferred
Stock” to 5,000,000 shares, filed June 31, 2016 (incorporated
by reference to Exhibit 10.1 to the Company’s Current Report
on Form 8-K filed April 7, 2016).
|
3.10
|
|
Certificate
of Amendment to the Certificate of Incorporation of Advanced
Medical Isotope Corporation, effective October 7, 2016
(incorporated by reference to Exhibit 3.1 to the Company’s
Current Report on Form 8-K filed on October 17, 2016).
|
5.1+
|
|
Opinion
of _________________________________.
|
10.1
|
|
Agreement
and Plan of Reorganization, dated as of December 15, 1998, by and
among HHH Entertainment, Inc. and Earth Sports Products, Inc.
(incorporated by reference to Exhibit 10.1 to the Company’s
Registration Statement on Form 10-12G (File No. 000-53497) filed on
November 12, 2008).
|
10.2
|
|
Agreement
and Plan of Merger of HHH Entertainment, Inc. and Savage Mountain
Sports Corporation, dated as of January 6, 2000 (incorporated by
reference to Exhibit 10.2 to the Company’s Registration
Statement on Form 10-12G (File No. 000-53497), filed on November
12, 2008).
|
10.3
|
|
Agreement
and Plan of Acquisition by and between Neu-Hope Technologies, Inc.,
UTEK Corporation and Advanced Medical Isotope Corporation, dated
September 22, 2006 (incorporated by reference to Exhibit 10.4 to
the Company’s Registration Statement on Form 10-12G (File No.
000-53497), filed on November 12, 2008).
|
10.4
|
|
Employment
Agreement dated May 16, 2007 with Leonard Bruce Jolliff
(incorporated by reference to Exhibit 10.5 to the Company’s
Registration Statement on Form 10-12G (File No. 000-53497), filed
on November 12, 2008).
|
10.5
|
|
Agreement
and Plan of Acquisition by and between Isonics Corporation and
Advanced Medical Isotope Corporation dated June 13, 2007
(incorporated by reference to Exhibit 10.6 to the Company’s
Registration Statement on Form 10-12G (File No. 000-53497), filed
on November 12, 2008).
|
10.6
|
|
Employment
Agreement dated January 15, 2008 with Dr. Fu-Min Su (incorporated
by reference to Exhibit 10.7 to the Company’s Registration
Statement on Form 10-12G (File No. 000-53497), filed on November
12, 2008).
|
10.7
|
|
Master
Lease Agreement dated September 20, 2007 between BancLeasing, Inc.
and Advanced Medical Isotope Corporation, and related documents
(incorporated by reference to Exhibit 10.8 to the Company’s
Annual Report on Form 10-K/A filed on December 2,
2011).
|
10.8
|
|
Lease
Agreement dated July 17, 2007 between Robert L. and Maribeth F.
Myers and Advanced Medical Isotope Corporation (incorporated by
reference to Exhibit 10.9 to the Company’s Annual Report on
Form 10-K/A filed on December 2, 2011).
|
10.9
|
|
Form of
Non-Statutory Stock Option Agreement (incorporated by reference to
Exhibit 10.1 to the Company’s Current Report on Form 8-K
filed on March 15, 2012).
|
10.10
|
|
Promissory
Note dated December 16, 2008 between Advanced Medical Isotope
Corporation and Carlton M. Cadwell (incorporated by reference to
Exhibit 10.11 to the Company’s Annual Report on Form 10-K
filed on March 3, 2012).
|
10.11
|
|
Memorandum
of Agreement for Strategic Relationship dated August 19, 2011
between Advanced Medical Isotope Corporation and Spivak Management
Inc. (incorporated by reference to Exhibit 10.12 to the
Company’s Annual Report on Form 10-K filed on March 3,
2012).
|
10.12
|
|
2015
Omnibus Securities and Incentive Plan
|
23.1*
|
|
Consent
of Fruci & Associates II, PLLC, Independent Registered
Public Accounting Firm i, r, p, a, f
|
23.2*
|
|
Consent
of Haynie & Company, Independent Registered Public Accounting
Firm i, r, p, a, f
|
24.1
|
|
Power
of Attorney, included in signature page to this registration
statement.
|
101.INS*
|
|
XBRL Instance Document
|
101.SCH*
|
|
XBRL
Taxonomy Extension Schema
|
101.CAL*
|
|
XBRL
Taxonomy Extension Calculation Linkbase
|
101.DEF*
|
|
XBRL
Taxonomy Extension Definition Linkbase
|
101.LAB*
|
|
XBRL
Taxonomy Extension Label Linkbase
|
101.PRE*
|
|
XBRL
Taxonomy Extension Presentation Linkbase
|
+ To be filed by amendment
* Filed herewith.
II-10