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EX-32.1 - EXHIBIT 32.1 - Artemis Therapeutics, Inc.exhibit_32-1.htm
EX-31.2 - EXHIBIT 31.2 - Artemis Therapeutics, Inc.exhibit_31-2.htm
EX-31.1 - EXHIBIT 31.1 - Artemis Therapeutics, Inc.exhibit_31-1.htm


UNITED STATES SECURITIES AND EXCHANGE COMMISSION
Washington, DC 20549

Form 10-Q

QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
 
For the quarterly period ended September 30, 2017
 
TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

(Commission file number 0-24431)
 
________________
 
ARTEMIS THERAPEUTICS, INC.
(Exact name of registrant as specified in its charter)

DELAWARE
84-1417774
(State or other jurisdiction of
(I.R.S. Employer Identification No.)
incorporation or organization)
 

18 East 16th Street, Suite 307, New York, NY
10003
(Address of principal executive offices)
(Zip Code)

(646) 233-1454
(Registrant’s telephone number, including area code)

(Former Name, Former Address and Former Fiscal Year, if Changed Since Last Report)

Indicate by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.
 
 Yes      No

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).
 
☒ Yes     ☐ No

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated non-accelerated filer, smaller reporting company, or an emerging growth company. See definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act. (Check one): 
 
 
Large accelerated filer
Accelerated filer
Non-accelerated filer (do not check if a smaller reporting company)
Smaller reporting company
Emerging growth company
 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.
 
Indicate by checkmark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).
 
Yes No

The number of shares of Common Stock of the registrant outstanding was 5,153,461 as of November 7, 2017.


ARTEMIS THERAPEUTICS, INC.
 
INDEX TO FORM 10-Q
 
 
 
PAGE
 
 
 
 
 
3
 
 
 
 
 
3
 
 
 
 
 
 
4
 
 
 
 
 
 
5
 
 
 
 
 
 
7
 
 
 
 
 
 
8
 
 
 
 
 
17
 
 
 
 
 
19
 
 
 
 
 
20
 
 
20
 
 
 
 
 
21
 
2

 
PART I.                      FINANCIAL INFORMATION

ITEM 1.                      FINANCIAL STATEMENTS
 
Artemis Therapeutics, Inc.
 
INTERIM CONDENSED CONSOLIDATED FINANCIAL STATEMENTS
 
AS OF SEPTEMBER 30, 2017
 
U.S. DOLLARS IN THOUSANDS
 
(UNAUDITED)
 
INDEX
 

3

 
Artemis Therapeutics, Inc.
Interim Condensed Consolidated Balance Sheets
(USD in thousands, except share data)
 
         
As of
September 30,
   
As of
December 31,
 
   
Note
   
2017 (Unaudited)
   
2016 (Audited)
 
                   
ASSETS
                 
                   
Current assets
                 
Cash and cash equivalents
         
345
     
907
 
Other accounts receivable and prepaid expenses
         
30
     
65
 
Total current assets
         
375
     
972
 
                       
TOTAL ASSETS
         
375
     
972
 
                       
LIABILITIES AND STOCKHOLDERS’ EQUITY
                     
                       
Current liabilities
                     
Accrued expenses and other payables
         
51
     
58
 
Total current liabilities
         
51
     
58
 
                       
Commitments and Contingencies
   
3   
     
-
     
-
 
                         
Total Liabilities
           
51
     
58
 
                         
Stockholders’ equity
                       
Preferred stock, $0.01 par value - Authorized: 10,000,000 shares; issued and outstanding: 453 shares as of September 30, 2017 and as of December 31, 2016
           
(*
)
   
(*
)
Common stock, $0.01 par value - Authorized: 51,000,000; issued and outstanding: 5,151,243 as of September 30, 2017 and 5,116,041 as of December 31, 2016
           
51
     
51
 
Additional paid in capital
   
7   
     
1,185
     
1,127
 
Accumulated deficit
           
(912
)
   
(264
)
Total stockholders’ equity
           
324
     
914
 
                         
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY
           
375
     
972
 
 
(*) Represents an amount lower than 1,000 USD
 
The accompanying notes are an integral part of the financial statements.
 
4


Artemis Therapeutics, Inc.
Interim Condensed Consolidated Statements of Operations
(USD in thousands, except share data)
 
   
Nine Months Ended September 30, 2017
   
For the period from April 19, 2016 (Inception), to September 30, 2016
   
Three Months Ended September 30, 2017
   
Three Months Ended September 30, 2016
 
                         
Research and development expenses
   
224
     
-
     
78
     
-
 
                                 
General and administrative
   
429
     
36
     
149
     
18
 
                                 
Operating loss
   
653
     
36
     
227
     
18
 
                                 
Finance Income
   
5
     
-
     
-
     
-
 
                                 
Net loss
   
648
     
36
     
227
     
18
 
                                 
Net loss used in the calculation of basic and diluted net loss per share (Note 6)
   
575
     
36
     
201
     
18
 
                                 
Net loss per share, basic and diluted (Note 6)
   
0.11
     
0.00
     
0.04
     
0.00
 
                                 
Weighted average number of common stock used in calculation of net loss per share:
Basic and diluted
   
5,126,614
     
4,552,745
     
5,147,417
     
4,841,119
 
 
The accompanying notes are an integral part of the financial statements.
 
5


Artemis Therapeutics, Inc.
Interim Condensed Statements of Changes in Stockholders’ Equity
(USD in thousands, except share data)
 
 
Common Stock
   
Preferred Stock
   
Additional paid-in
   
Accumulated
   
Total shareholders’
 
   
Number of Shares
   
USD
   
Number
   
Amount
   
Capital
   
(deficiency)
   
equity
 
                                           
Balance as of December 31, 2016 (**)
   
5,116,041
     
51
     
453
     
(*
)
   
1,127
     
(264
)
   
914
 
                                                         
Share based compensation
                                   
58
             
58
 
                                                         
Exercised options
   
35,202
     
(*
)
                                   
(*
)
                                                         
Net loss for nine months ended September 30, 2017
                                           
(648
)
   
(648
)
                                                         
Balance as of September 30, 2017
   
5,151,243
     
51
     
453
     
(*
)
   
1,185
     
(914
)
   
324
 

(*) Represents an amount lower than 1,000 USD

(**) Share data as of December 31, 2016 is restated (Note 8)
 
The accompanying notes are an integral part of the financial statements.
 
 
6


Artemis Therapeutics, Inc.
Interim Condensed Consolidated Statements of Cash Flows (Unaudited)
(USD in thousands)
 
   
Nine Months Ended September 30, 2017
   
For the period from April 19, 2016 (Inception), to September 30, 2016
   
Three Months Ended September 30, 2017
   
Three Months Ended September 30, 2016
 
                         
Net cash used in operating activities
                       
Net Loss
   
(648
)
   
(36
)
   
(227
)
   
(18
)
                                 
Share based compensation expenses
   
58
     
-
     
11
     
-
 
Decrease in other accounts receivable and prepaid expenses
   
35
     
-
     
10
     
-
 
Decrease in accrued expenses and other payables
   
(7
)
   
(19
)
   
(4
)
   
(36
)
                                 
Net cash used in operating activities
   
(562
)
   
(55
)
   
(210
)
   
(55
)
                                 
Cash flows from financing activities
                               
Exercise of options
   
(*
)
   
-
     
(*
)
   
-
 
Issuance of common stock
   
-
     
481
     
-
     
481
 
Acquisition of subsidiary in connection with a reverse acquisition
   
-
     
575
     
-
     
575
 
Cash flows from financing activities
   
(*
)
   
1,056
     
(*
)
   
1,056
 
                                 
Increase (decrease) in cash and cash equivalents
   
(562
)
   
1,001
     
(210
)
   
1,001
 
Cash and cash equivalents at the beginning of the period
   
907
     
-
     
555
     
-
 
                                 
Cash and cash equivalents at the end of the period
   
345
     
1,001
     
345
     
1,001
 
                                 
(*) Represents an amount lower than 1,000 USD
                               
 
The accompanying notes are an integral part of the financial statements.
7

 
Artemis Therapeutics, Inc.
Notes to the Interim Condensed Consolidated Financial Statements
(USD in thousands)
 
NOTE 1 -   GENERAL

 
A.
New York Global Innovations Inc. (the “Predecessor Company”) was originally incorporated under the laws of the State of Nevada, on April 22, 1997. On July 8, 2003, the Predecessor Company effected a reincorporation from Nevada to Delaware through a merger with and into its wholly-owned subsidiary, Inksure Technologies (Delaware) Inc., which was incorporated on September 30, 2003. The surviving corporation in the merger was Inksure Technologies (Delaware) Inc., which thereupon renamed itself Inksure Technologies Inc. In 2014, following the sale of its assets to Spectra Systems Corporation, the Predecessor Company changed its name to New York Global Innovations Inc.
 
On August 23, 2016, the Predecessor Company consummated an agreement and plan of merger (the “Merger Agreement”) with Artemis Pharma Inc. (formerly, Artemis Therapeutics Inc.), a Delaware corporation (“Artemis”) and its wholly-owned subsidiary, Artemis Acquisition Corp., a Delaware corporation (“Merger Subsidiary”). Pursuant to the terms of the Merger Agreement, Artemis merged with and into the Merger Subsidiary, with Artemis being the surviving entity (the “Merger”).  Following the Merger, the Company adopted the business plan of Artemis and Artemis became a wholly-owned subsidiary of the Company.  On December 16, 2016, the Company changed its name to Artemis Therapeutics, Inc.  In exchange for the outstanding shares of Artemis, the Company issued to Artemis shareholders a total of 460,000 shares (as adjusted to reflect the reverse stock split) of the Predecessor Company’s common stock and series B convertible preferred stock convertible into 3,724,225 shares (as adjusted to reflect the reverse stock split). All series B preferred shares were converted to common shares prior to December 31, 2016. Immediately following the consummation of the Merger, Artemis stockholders owned approximately 82% of the Company’s common stock on a fully diluted basis. Following the issuance and sale of the Company’s Series A Preferred Stock and common stock to an investor, Artemis stockholders owned approximately 73% of the Company’s common stock on a fully diluted basis. (Refer to Note 7).

The Company’s fiscal year end is December 31.
 
8

 
Artemis Therapeutics, Inc.
Notes to the Interim Condensed Consolidated Financial Statements
(USD in thousands)
 
 NOTE 1 -  GENERAL (cont.)
 
The Merger between the Predecessor Company and Artemis was accounted for as a reverse recapitalization and, as a result of the Merger, the Predecessor Company ceased to be a shell company. As the shareholders of Artemis received the largest ownership interest in the Predecessor Company, Artemis was determined to be the “accounting acquirer” in the reverse acquisition. As a result, the historical financial statements of the Predecessor Company were replaced with the historical financial statements of Artemis. Following the Merger, the Predecessor Company and its subsidiary, Artemis, are collectively referred to as the “Company”.
 
 
B.
Establishment of Artemis (the “accounting acquirer”):
 
Artemis was incorporated in the State of Delaware on April 19, 2016. Artemis is engaged in the development of agents for the prevention and treatment of severe and potentially life-threatening infectious diseases. Artemis’s lead product candidate, Artemisone, is a clinical-stage synthetic artemisinin derivative with antiviral and antiparasitic properties. Artemis expects to advance Artemisone initially as an antiviral agent to address unmet clinical needs in the growing population of immunocompromised patients infected with human cytomegalovirus (HCMV), and other related clinical indications.

On May 31, 2016, Artemis entered into a license agreement with Hadasit Medical Research Services & Development Ltd. (“Hadasit”), and Hong Kong University of Science and Technology R and D Corporation Limited (“RDC”), pursuant to which Artemis acquired a worldwide, royalty-bearing license to make any and all use of certain patents and know-how owned by the Hadasit and RDC relating to Artemisone. Artemis will rely primarily on the license agreement with respect to the development of Artemisone, its lead product candidate.

Artemis has not generated any revenues from its activities and has incurred substantial operating losses. Management expects Artemis to continue to generate substantial operating losses and to continue to fund its operations primarily through additional raises of capital. Such conditions raise substantial doubts about the Company’s ability to continue as a going concern. These financial statements do not include any adjustments relating to the recoverability and classification of assets, carrying amounts or the amount and classification of liabilities that may be required should the Company be unable to continue as a going concern.
 
NOTE 2 -   BASIS OF PRESENTATION AND SIGNIFICANT ACCOUNTING POLICIES
 
 
A.
Unaudited Interim Financial Statements
 
The accompanying unaudited interim condensed financial statements have been prepared in accordance with U.S. generally accepted accounting principles (“GAAP”) for interim financial information and with the instructions to Form 10-Q and Article 10 of U.S. Securities and Exchange Commission Regulation S-X. Accordingly, they do not include all the information and footnotes required by GAAP for complete financial statements. In the opinion of management, all adjustments considered necessary for a fair presentation have been included (consisting only of normal recurring adjustments except as otherwise discussed). For further information, reference is made to the consolidated financial statements and footnotes thereto included in the Company’s Annual Report on Form 10-K for the year ended December 31, 2016. Operating results for the nine months ended September 30, 2017, are not necessarily indicative of the results that may be expected for the year ended December 31, 2017.
 
9

Artemis Therapeutics, Inc.
Notes to the Interim Condensed Consolidated Financial Statements
(USD in thousands)
 
NOTE 2 -   BASIS OF PRESENTATION AND SIGNIFICANT ACCOUNTING POLICIES (Cont.)
 
  B.
Significant Accounting Policies
 
The significant accounting policies followed in the preparation of these unaudited interim condensed consolidated financial statements are identical to those applied in the preparation of the latest annual financial statements.
 
 
C.
Recent Accounting Standards:

In May 2014, the Financial Accounting Standards Board (the “FASB”) issued a new standard to achieve a consistent application of revenue recognition within the U.S., resulting in a single revenue model to be applied by reporting companies under U.S. generally accepted accounting principles. Under the new model, recognition of revenue occurs when a customer obtains control of the promised goods or services in an amount that reflects the consideration to which the entity expects to be entitled in exchange for those goods or services. In addition, the new standard requires that reporting companies disclose the nature, amount, timing, and uncertainty of revenue and cash flows arising from contracts with customers. The new standard is effective with respect to the Company beginning in the first quarter of 2018; early adoption is prohibited. The new standard is required to be applied retrospectively to each prior reporting period presented or retrospectively with the cumulative effect of initially applying it recognized at the date of initial application. As the Company has not incurred revenues to date, it is unable to determine the expected impact the new standard will have on its consolidated financial statements.

In February 2016, the FASB issued a new lease accounting standard requiring the recognition of lease assets and liabilities on the balance sheet. This standard is effective beginning in the first quarter of 2019; early adoption is permitted. The Company does not expect the adoption of this standard to have a material impact on its consolidated financial statements.

In June 2016, the FASB issued ASU 2016-13, “Financial Instruments - Credit Losses: Measurement of Credit Losses on Financial Instruments.” With respect to assets measured at amortized cost, such as held-to-maturity assets, the update requires presentation of the amortized cost net of a credit loss allowance. The update eliminates the probable initial recognition threshold that was previously required prior to recognizing a credit loss on financial instruments. The credit loss estimate can now reflect an entity’s current estimate of all future expected credit losses as opposed to the previous standard, when an entity only considered past events and current conditions. With respect to available for sale debt securities, the update requires that credit losses be presented as an allowance rather than as a write-down. The update is effective beginning in the first quarter of 2020; early adoption is permitted. The Company does not expect the adoption of this standard to have a material impact on its consolidated financial statements.

10

Artemis Therapeutics, Inc.
Notes to the Interim Condensed Consolidated Financial Statements
(USD in thousands)
 
NOTE 2 -   BASIS OF PRESENTATION AND SIGNIFICANT ACCOUNTING POLICIES (Cont.)

In May 2017, the FASB issued “ASU No. 2017-09, “Compensation-Stock Compensation (Topic 718): Scope of Modification Accounting,” which clarifies when a change to terms or conditions of a share-based payment award must be accounted for as a modification. The new guidance requires modification accounting if the vesting condition, fair value or the award classification is not the same both before and after a change to the terms and conditions of the award. The new guidance is effective on a prospective basis beginning on January 1, 2018 and early adoption is permitted. The Company does not expect the adoption of this standard to have a material impact on its consolidated financial statements.

In July 2017, the FASB issued ASU 2017-11, which includes Part I “Accounting for Certain Financial Instruments with Down Round Features” and Part II “Replacement of the Indefinite Deferral for Mandatorily Redeemable Financial Instruments of Certain Nonpublic Entities and Certain Mandatorily Redeemable Non-controlling Interests With a Scope Exception”. The ASU makes limited changes to the Board’s guidance on classifying certain financial instruments as either liabilities or equity. The ASU’s objective is to improve (1) the accounting for instruments with “down-round” provisions and (2) the readability of the guidance in ASC 480 on distinguishing liabilities from equity by replacing the indefinite deferral of certain pending content with scope exceptions. This standard is effective beginning in the first quarter of 2019; early adoption is permitted. The Company does not expect the adoption of this standard to have a material impact on its consolidated financial statements.
 
NOTE 3   - COMMITMENTS AND CONTINGENCIES
        
Agreement with Hadasit and RDC
 
On May 31, 2016, Artemis entered into the License Agreement with Hadasit and RDC, pursuant to which Artemis acquired a worldwide, royalty-bearing license to make any and all use of certain patents and know-how owned by the Hadasit and RDC relating to Artemisone. Artemis will rely primarily on the License Agreement with respect to the development of Artemisone, its lead product candidate.
 
NOTE 4 -   INCOME TAX
 
 
A.
Tax rates applicable to the income

The Company is subject to a blended US tax rate (Federal as well as State Corporate Tax) of 35% in 2016. The Company’s subsidiary in Israel is subject to income tax at a regular corporate tax 25% in 2016.

In December 2016, legislation to amend the corporate income tax law in Israel was published. The legislation determined a decrease of the corporate income tax law as of January 1, 2017 to 24% (1% decrease) and as of January 1, 2018 to 23% (additional 1% decrease).

11

Artemis Therapeutics, Inc.
Notes to the Interim Condensed Consolidated Financial Statements
(USD in thousands)
 
NOTE 4 -   INCOME TAX (Cont.)
 
 
B.
Deferred income taxes
 
As the Company is still in its development stage and has not yet generated revenues, it is more likely than not that sufficient taxable income will not be available for the tax losses to be utilized in the future. Therefore, a valuation allowance was recorded to reduce the deferred tax assets to its recoverable amounts.
 
   
As of September 30, 2017
   
As of December 31, 2016
 
Deferred tax assets:
           
Deferred taxes due to carryforward losses
   
3,693
     
3,583
 
                 
Valuation allowance
   
(3,693
)
   
(3,583
)
                 
Net deferred tax asset
   
-
     
-
 
 
 
C.
Tax loss carry-forwards

Net operating loss carry-forwards as of September 30, 2017 are as follows:

   
As of September 30, 2017
   
As of December 31, 2016
 
Israel                                                   
   
4,742
     
4,518
 
United States (*)
   
7,435
     
7,011
 
                 
     
12,177
     
11,529
 
  
Net operating losses in Israel may be carried forward indefinitely. Net operating losses in the U.S. are available through 2027.

(*) Utilization of U.S. net operating losses may be subject to substantial annual limitation due to the “change in ownership” provisions of the Internal Revenue Code of 1986, as amended, and similar state provisions. The annual limitation may result in the expiration of net operating losses before utilization.

12

Artemis Therapeutics, Inc.
Notes to the Interim Condensed Consolidated Financial Statements
(USD in thousands)
 
NOTE 5 -   WARRANTS ISSUED TO INVESTORS
 
In connection with historical financings, the Company issued warrants to investors as follows:
 
ISSUANCE DATE
 
OUTSTANDING
AS OF December 31, 2016 and
September 30, 2017 *
   
EXERCISE PRICE
 
EXERCISABLE THROUGH
 
           
        
January 2010 **
   
43,069
   
$
0.055
 
April 2018
 
* Amount of warrants is retroactively adjusted to reflect the 1 to 50 reverse stock split
 
NOTE 6 -   Computation of Net Loss per Share
 
Basic loss per share is computed by dividing the net loss, as adjusted to include preferred shares dividend participation rights, by the weighted average number of common stock outstanding during the year.
 
Diluted loss per share is computed by dividing the net loss, as adjusted to include preferred shares dividend participation rights, of preferred shares outstanding during the year as well as of preferred shares that would have been outstanding if all potentially dilutive preferred shares had been issued, by the weighted average number of common stock outstanding during the year, plus the number of common stock that would have been outstanding if all potentially dilutive common stock had been issued, using the treasury stock method, in accordance with ASC 260-10 “Earnings per Share”.
 
The loss and weighted average number of common stock used in the calculation of basic loss per share are as follows (in thousands, except share and per share data):
 
 
 
Nine Months
Ended
September 30,
2017
   
The period from April 19 (Inception), 2016 to September 30, 2016
   
Three Months
Ended
September 30, 2017
   
Three Months
Ended
September 30, 2016
 
Net loss available to shareholders of the company
   
(648
)
   
(36
)
   
(227
)
   
(18
)
Net loss attributable to shareholders of preferred shares and to shareholders of preferred shares contingently issuable for little or no cash
   
73
     
4
     
26
     
2
 
 
                               
Net loss used in the calculation of basic loss per share
   
(575
)
   
(32
)
   
(201
)
   
(16
)
 
                               
Net loss per share
   
0.11
     
0.00
     
0.04
     
0.00
 
 
                               
Weighted average number of common stock
   
5,126,614
     
4,552,745
     
5,147,416
     
4,841,119
 
 
 
13

Artemis Therapeutics, Inc.
Notes to the Interim Condensed Consolidated Financial Statements
(USD in thousands)
 
NOTE 7 -   STOCK CAPITAL
 
  A.
Stockholders Rights:
 
Shares of common stock confer upon their holders the right to receive notice to participate and vote in general meetings of shareholders of the Company, the right to receive dividends, if declared, and the right to receive a distribution of any surplus of assets upon liquidation of the Company.
 
  B.
Issuance of Shares:
 
On August 19, 2016 and prior to consummation of the merger, Artemis issued 524 shares of common stock (238,629 shares as adjusted to reflect the reverse recapitalization and reverse stock split) for an aggregate purchase price of $127 which was received in October 2016.
 
In August 2016, immediately upon consummation of the Merger, the Company issued 68,321 shares of the Company’s common stock, as well as 453 shares of the Company’s newly designated Series A Convertible Preferred Stock convertible into 658,498 shares of common stock, to an investor for an aggregate purchase price of $481,000 (net of issuance expenses).
 
Preferred shares confer upon their holders the right to receive dividends when paid to holders of common stock of the Company on an as-converted basis, and the right to receive a distribution of any surplus of assets upon liquidation of the Company before any distribution or payment shall be made to the holders of any junior securities.
 
  C.
Reverse Stock Split:
 
On December 16, 2016, the Company effected a one-for-fifty (1:50) reverse stock split of its issued and outstanding shares of common stock. Share data included in these financial statements is retroactively adjusted as if the reverse stock split had occurred at the beginning of the earliest period presented.
 
  D.
Options issued to consultants:
 
On August 22, 2016, the Company granted 126,730 stock options to consultants. Each stock option is exercisable into a share of the Company’s common stock of and expires no later than 10 years from the date of grant.
 
One third of the options vested on the grant date, and one third of the options vest upon the first and second anniversaries of the grant date, with the option becoming fully vested on August 22, 2018. As a result, the Company recognized compensation expenses in the amount of $58, included in Research and Development Expenses. 35,202 of these options were exercised in July 2017.
 
14

Artemis Therapeutics, Inc.
Notes to the Interim Condensed Consolidated Financial Statements
(USD in thousands)
 
NOTE 7 -   STOCK CAPITAL (Cont.)
 
A summary of the Company’s option activity and related information is as follows:
 
   
For the nine months ended
September 30, 2017
 
   
Number of stock options
   
Weighted average exercise price
   
Aggregate intrinsic value
 
Outstanding at beginning of period
   
126,730
             
Granted
   
-
             
Exercised
   
35,202
             
Cancelled
   
-
             
                     
Outstanding at end of period
   
91,528
   
$
0.01
     
113,494
 
Options exercisable at period end
   
49,285
   
$
0.01
     
61,113
 
 
The aggregate intrinsic value in the table above represents the total intrinsic value (the difference between the fair market value of the Company’s common stock on September 30, 2017, and the exercise price, multiplied by the number of in-the-money stock options on those dates) that would have been received by the stock option holders had all stock option holders exercised their stock options on those dates.
 
The stock options outstanding as of September 30, 2017, have been separated into exercise price, as follows:
 
Exercise price
   
Stock options outstanding as of September 30,
   
Weighted average remaining contractual life – years as of September 30,
   
Stock options exercisable as of September 30,
 
$    
2 0 1 7
   
2017
   
2017
 
                     
 
0.01
     
126,730
     
8.9
     
49,285
 
 
As the exercise price of the options is nominal, the Company estimated their fair values based on the value of the Company’s shares at the measurement date.
 
15


Artemis Therapeutics, Inc.
Notes to the Interim Condensed Consolidated Financial Statements
(USD in thousands)
 
NOTE 8 -   Convertible preferred stock Series A and common stock - Restatement
 
As explained in note 6, the Company issued preferred shares to one of its shareholders. The shares are convertible to common shares at any point in time and participate in earning on an as converted basis. The Company in its previous fillings erroneously presented these shares as if the shares had been converted to common shares.

In Addition, as explained in note 7, the Company effected a one-for-fifty (1:50) reverse stock split of its issued and outstanding shares of common stock. The par value of $0.01 per share did not change as a result of the reverse stock split. The Company in its previous filings erroneously presented its par value and share premium line items based on a $0.5 par value per share.
 
The following tables present the restated financial statements line items:
 
Artemis Therapeutics, Inc.
Condensed Consolidated Statements Balance Sheet
(Audited)
 
   
December 31, 2016
 
   
As Reported
   
Adjustments
   
As Restated
 
                   
Shareholders’ equity
                 
Preferred stock, $0.01 par value - Authorized: 10,000,000 shares; issued and outstanding: 0 and 453 shares (as reported and as restated) as of December 31, 2016
   
-
     
(*
)
   
(*
)
Common stock, $0.01 par value - Authorized: 51,000,000; issued and outstanding: 5,774,549 and 5,116,041 (as reported and as restated) as of December 31, 2016
   
2,887
     
(2836
)
   
51
 
Additional paid in capital
   
(1,709
)
   
2,836
     
1,127
 
Accumulated deficit
   
(264
)
   
-
     
(264
)
Total shareholders’ equity
   
914
     
-
     
914
 
 
(*) Represents an amount lower than 1,000 USD
 
NOTE 9 -   Subsequent Events
 
On October 23, 2017, the Company executed Securities Purchase Agreements (each, a “Securities Purchase Agreement”) with a total of 6 accredited investors relating to a private placement offering (the “Offering”) of an aggregate of 300,000 shares of the Company’s common stock, $0.01 par value per share, at a purchase price of $1.00 per share, and of 250 shares of the Company’s newly designated Series C Convertible Preferred Stock (the “Series C Preferred Stock”), at a purchase price of $1,000.00 per share, with such shares of Series C Preferred Stock initially convertible into an aggregate of 250,000 shares of Common Stock (subject to adjustment for future price-based and customary stock-based anti-dilution protections). In addition, each investor received a warrant (each, a “Warrant”) to purchase fifty percent of the number of shares of Common Stock effectively purchased in the Offering, for an aggregate of 275,000 shares of Common Stock, at an exercise price of $2.00 per share. The closing of the Offering took place on October 23, 2017.
 
16

 
ITEM 2.              MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
 
In this section, “Management’s Discussion and Analysis of Financial Condition and Results of Operation,” references to “the Company” “we,” “us,” or “our,”  refer to Artemis Therapeutics, Inc. and its consolidated subsidiaries and dollar amounts are in thousands, except as otherwise stated.
 
This Quarterly Report on Form 10-Q contains statements that may constitute “forward-looking statements.” Generally, forward-looking statements include words or phrases such as “anticipates,” “believes,” “estimates,” “expects,” “intends,” “plans,” “projects,” “could,” “may,” “might,” “should,” “will,” the negative of such terms, and words and phrases of similar import. For example, when we discuss possible strategic alternatives, we are using forward-looking statements.  Such statements are based on management’s current expectations and are subject to a number of risks and uncertainties, including, but not limited to, the risks detailed from time to time in our filings with the Securities and Exchange Commission, or the SEC. These risks and uncertainties could cause our actual results to differ materially from those described in our forward-looking statements. Any forward-looking statement represents our expectations or forecasts only as of the date it was made and should not be relied upon as representing its expectations or forecasts as of any subsequent date. Except as required by law, we undertake no obligation to correct or update any forward-looking statement, whether as a result of new information, future events or otherwise, even if our expectations or forecasts change.
 
The following discussion and analysis should be read in conjunction with the financial statements, related notes and other information included in this Quarterly Report on Form 10-Q and with the Risk Factors included in Part I, Item 1A of our Annual Report on Form 10-K.
 
OVERVIEW
 
We are a biopharmaceutical company dedicated to the development of novel, safe, and effective agents for the prevention and treatment of severe and potentially life-threatening infectious diseases. Our lead product candidate, artemisone, is a clinical-stage synthetic artemisinin derivative with antiviral and antiparasitic properties. We expect to advance artemisone initially as an antiviral agent to address unmet clinical needs in the growing population of immunocompromised patients infected with human cytomegalovirus and as an antiparasitic agent to address unmet needs such as resistance in malaria-infected individuals, and other related clinical indications.

On August 23, 2016, we consummated a merger with Artemis Therapeutics Inc., a Delaware corporation (“Artemis Subsidiary”) and Artemis Acquisition Corp., a Delaware corporation and our wholly-owned subsidiary (the “Merger Subsidiary”), pursuant to which Artemis Subsidiary merged with and into the Merger Subsidiary, with Artemis Subsidiary being the surviving entity (the “Merger”).  Following the Merger, we adopted the business plan of Artemis Subsidiary.

On May 31, 2016, we entered into a license agreement (the “License Agreement”) by and among us, Hadasit Medical Research Services and Development Ltd. (“Hadasit”) and Hong Kong University of Science and Technology R and D Corporation Limited (“RDC”), pursuant to which we acquired a worldwide, royalty-bearing license to make any and all use of certain patents and know-how owned by the Hadasit and RDC relating to artemisone. We will rely primarily on the License Agreement with respect to the development of artemisone, our lead product candidate.

To date, we have not generated revenue from the sale of our lead product candidate and do not anticipate generating any revenue for an extended period of time. Our financing activities are described below under “Liquidity and Capital Resources.”

THREE MONTHS ENDED SEPTEMBER 30, 2017 COMPARED TO THE THREE MONTHS ENDED SEPTEMBER 30, 2016 (dollars in thousands)
 
REVENUES.  We did not have any revenue producing operations for the three months ended September 30, 2017 and for the three month period ended September 30, 2016.

17

COST OF REVENUES. We had no cost of revenues for the three months ended September 30, 2017 and for the three month period ended September 30, 2016 due to the fact that we had no revenue-producing operations.
 
RESEARCH AND DEVELOPMENT EXPENSES. We incurred research and development expenses in the amount of $78 for the three months ended September 30, 2017 compared to zero for the three month period ended September 30, 2016. The research and development expenses consisted primarily of consulting services, patent expenses and option expenses. We did not capitalize research and development expenses as all such expenses were charged to operating expenses as incurred. The increase in research and development expenses is due to our having no research and development expenses prior to the Merger.

SELLING AND MARKETING EXPENSES. We did not incur any selling and marketing expenses for the three months ended September 30, 2017 or for the three month period ended September 30, 2016, due to our being in our developmental stage.

GENERAL AND ADMINISTRATIVE EXPENSES. We incurred $149 in general and administrative expenses for the three months ended September 30, 2017 compared to $18 for the three month period ended September 30, 2016,  which consisted primarily of compensation costs for administrative, finance and general management personnel, insurance, legal, accounting and administrative costs. The increase in general and administrative expenses is due to our having minimal expenses prior to the Merger.
 
FINANCIAL INCOME, NET. We incurred no financial income for the three months ended September 30, 2017 and for the three month period ended September 30, 2016.
 
NET PROFIT (LOSS). We incurred a net loss of $227 in the three months ended September 30, 2017 compared to $18 for the three month period ended September 30, 2016. The expenses are primarily related to our operational expenses. The increase in net loss is due to our having minimal expenses prior to the Merger and current operating expenses comprised of $78 in research and development expenses and $149 in general and administrative expenses.

NINE MONTHS ENDED SEPTEMBER 30, 2017 COMPARED TO THE PERIOD FROM APRIL 19 (INCEPTION), 2016 TO SEPTEMBER 30, 2016 (dollars in thousands)
 
REVENUES.  We did not have revenue-producing operations for the nine months ended September 30, 2017 and for the period from April 19 (Inception), 2016 to September 30, 2016.

COST OF REVENUES. We had no cost of revenues for the nine months ended September 30, 2017 and for the period from April 19 (Inception), 2016 to September 30, 2016 due to the fact that we had no revenue-producing operations.
 
RESEARCH AND DEVELOPMENT EXPENSES. We incurred $224 in research and development expenses for the nine months ended September 30, 2017 compared to zero for the period from April 19 (Inception), 2016 to September 30, 2016. The research and development expenses consisted primarily of consulting services, patent expenses and option expenses. We did not capitalize research and development expenses in the nine months ended September 30, 2017, as all such expenses were charged to operating expenses as incurred. The increase in research and development expenses is due to our having no research and development expenses prior to the Merger.

SELLING AND MARKETING EXPENSES. We did not incur any selling and marketing expenses for the nine months ended September 30, 2017 and for the period from April 19 (Inception), 2016 to September 30, 2016, due to our being in its developmental stage.

GENERAL AND ADMINISTRATIVE EXPENSES. We incurred $429 in general and administrative expenses for the nine months ended September 30, 2017 compared to $36 for the period from April 19 (Inception), 2016 to September 30, 2016. The general and administrative expenses consisted primarily of compensation costs for administrative, finance and general management personnel, insurance, legal, accounting and administrative costs. The increase in general and administrative expenses is due to our having minimal expenses prior to the Merger.

18

FINANCIAL INCOME, NET. We incurred financial income of $5 for the nine months ended September 30, 2017 compared to zero for the period from April 19 (Inception), 2016 to September 30, 2016.
 
NET PROFIT (LOSS). We incurred a net loss of $648 in the nine months ended September 30, 2017, compared to $36 for the period from April 19 (Inception), 2016 to September 30, 2016 which was primarily related to our operational expenses. The increase in net loss is due to our having minimal expenses prior to the Merger.

LIQUIDITY AND CAPITAL RESOURCES (dollars in thousands)
 
As of September 30, 2017, we had an accumulated deficit of $912 and a positive working capital (current assets less current liabilities) of $324. Losses will probably continue for the foreseeable future.
 
We do not have any material capital commitments for capital expenditures as of September 30, 2017.

We have sustained significant operating losses in recent periods, which has resulted in a significant reduction in our cash reserves.  We have not been profitable and we cannot predict when we will achieve profitability. We experienced net losses and have had no revenues since Artemis’ inception in April 2016. We do not anticipate generating significant revenues until we successfully develop, commercialize and sell our proposed products, of which we can give no assurance. We are unable to determine when we will generate significant revenues, if any, from the sale of any of such products.  As of September 30, 2017, we had accumulated liabilities of $51.

As of September 30, 2017, we had cash and cash equivalents of $345, and negative cash flows from operating activities of $562 for the period then ended. The negative cash flow from operating activities in the period ended September 30, 2017 is attributable mainly to the net loss of $648, share-based compensation expenses of $58, a decrease in accrued expenses and other payables of $3, and a $35 decrease in other accounts receivable and prepaid expenses.
 
We did not have any cash flows from or used for financing or investing activities for the period ended September 30, 2017.
 
On October 23, 2017, we executed securities purchase agreements with a total of 6 accredited investors relating to a private placement offering (the “Offering”) of an aggregate of 300,000 shares of our common stock, $0.01 par value per share, at a purchase price of $1.00 per share (the “Common Stock”), and of 250 shares of our newly designated Series C Convertible Preferred Stock (the “Series C Preferred Stock”), at a purchase price of $1,000 per share, with such shares of Series C Preferred Stock initially convertible into an aggregate of 250,000 shares of Common Stock. In addition, each investor received a warrant to purchase fifty percent of the number of shares of Common Stock effectively purchased in the Offering, for an aggregate of 275,000 shares of Common Stock. The closing of the Offering took place on October 23, 2017 and we received aggregate net proceeds of $550,000.

CONTRACTUAL OBLIGATIONS AND COMMITMENTS
 
None.
 
 OFF BALANCE SHEET ARRANGEMENTS
 
None.
 
ITEM 4.              CONTROLS AND PROCEDURES
 
Under the direction of the Interim Chief Executive Officer and Chief Financial Officer, we evaluated our disclosure controls and procedures and concluded that our disclosure controls and procedures were effective as of September 30, 2017.
 
No change in our internal control over financial reporting occurred during the quarter ended September 30, 2017 that has materially affected, or is reasonably likely to materially affect, such internal control over financial reporting.
 
19

 
PART II.                    OTHER INFORMATION
 
ITEM 6.                      EXHIBITS
 
The following exhibits are being filed or furnished with this Report:
 
EXHIBIT
NUMBER
 
DESCRIPTION
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
101.1
 
The following materials from the Company’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2017, formatted in XBRL (eXtensible Business Reporting Language): (i) the Condensed Consolidated Balance Sheet, (ii) the Condensed Consolidated Statements of Operations, (iii) the Condensed Consolidated Statements of Cash Flows and (iv) related notes to these financial statements, tagged as blocks of text and in detail.*
 
* Filed herewith
 
**Furnished herewith
 
20

 
SIGNATURES
 
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
 
 
 
ARTEMIS THERAPEUTICS, INC.
 
 
Dated: November 13, 2017
By: /s/ Brian Culley
 
Brian Culley
 
Interim Chief Executive Officer
(Principal Executive Officer)
 
 
 
 
Dated: November 13, 2017
By: /s/ Chanan Morris
 
Chanan Morris
 
Chief Financial Officer
 
(Principal Financial and Accounting Officer)
 
 
 
21