Attached files
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8-K - FORM 8-K - INOVIO PHARMACEUTICALS, INC. | w81311e8vk.htm |
EX-4.1 - EX-4.1 - INOVIO PHARMACEUTICALS, INC. | w81311exv4w1.htm |
EX-1.1 - EX-1.1 - INOVIO PHARMACEUTICALS, INC. | w81311exv1w1.htm |
EX-5.1 - EX-5.1 - INOVIO PHARMACEUTICALS, INC. | w81311exv5w1.htm |
EX-10.1 - EX-10.1 - INOVIO PHARMACEUTICALS, INC. | w81311exv10w1.htm |
Exhibit 99.1

NEWS RELEASE
For Immediate Release
CONTACTS: |
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Investors:
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Bernie Hertel, Inovio Pharmaceuticals 858-410-3101 bhertel@inovio.com | |
Media:
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Jeff Richardson, Richardson & Associates 805-491-8313 jeff@richardsonglobalpr.com |
Inovio Pharmaceuticals Announces $24.3 Million Registered Offering
BLUE BELL, PA Jan. 24, 2011 Inovio Pharmaceuticals, Inc. (NYSE Amex: INO), a leader in
the development of therapeutic and preventive vaccines against cancers and infectious diseases,
announced today that it has agreed to sell to a single institutional investor 21,130,400 shares of
its common stock and warrants to purchase up to 10,565,200 additional shares of its common stock.
The shares of common stock and warrants are being offered in units consisting of one share of
common stock and 0.5 of a warrant to purchase one share of common stock at a price of $1.15 per
unit. The warrants have a term of five years and an exercise price of $1.40 per share. Inovio may
call these warrants if the closing bid price of the common stock has been at least $2.80 over 20
trading days and certain other conditions are met.
The gross proceeds of the offering are expected to be $24.3 million and net proceeds, after
deducting the placement agents fee and estimated offering expenses payable by Inovio, are expected
to be approximately $23.0 million. Roth Capital Partners, LLC acted as the sole placement agent in
the offering. Brean Murray, Carret & Co. and Rodman & Renshaw, LLC served as financial advisors to
the Company in the offering.
Inovio intends to use proceeds from the offering for further development of its DNA vaccine against
cervical dysplasias and cancers, other preclinical and clinical studies, and general corporate
purposes. The offering is expected to close on or about January 27, 2011, subject to the
satisfaction of customary closing conditions.
This financing will fully fund our planned Phase II clinical study for our DNA vaccine against
cervical dysplasias and cancers, as well as other clinical studies that Inovio intends to directly
fund and launch in 2011. The additional capital will also allow us to more rapidly advance other
promising preclinical DNA vaccine programs toward the clinic, and we believe we now have sufficient
cash to cover our operations into 2014, noted Dr. J. Joseph Kim, President and CEO.
The securities described above are being offered by Inovio pursuant to a registration statement
previously filed and declared effective by the Securities and Exchange Commission, or the SEC. A
prospectus supplement related to the offering will be filed with the SEC. Copies of the prospectus
supplement and accompanying base prospectus relating to this offering may be obtained at the SECs
website at www.sec.gov or from Roth Capital Partners, LLC by e-mail to rothecm@roth.com or by mail
to 1787 Sentry Parkway West, Building 18, Suite 400, Blue Bell, Pennsylvania 19422. This
announcement is
neither an offer to sell nor a solicitation of an offer to buy any of our common
stock. No offer, solicitation or sale will be made in any jurisdiction in which such offer,
solicitation or sale is unlawful.
About Inovio Pharmaceuticals, Inc.
Inovio is developing a new generation of vaccines, called DNA vaccines, to treat and prevent
cancers and infectious diseases. These SynCon vaccines are designed to provide broad cross-strain
protection against known as well as newly emergent strains of pathogens such as influenza. These
vaccines, in combination with Inovios proprietary electroporation delivery devices, have been
shown to be safe and generate significant immune responses. Inovios clinical programs include
HPV/cervical dysplasia and cancer (therapeutic), avian flu (preventive), and HIV vaccines (both
preventive and therapeutic). Inovio is developing universal influenza and other vaccines in
collaboration with scientists from the University of Pennsylvania. Other partners and collaborators
include Merck, National Cancer Institute, U.S. Military HIV Research Program, NIH, HIV Vaccines
Trial Network, National Microbiology Laboratory of the Public Health Agency of Canada, and PATH
Malaria Vaccine Initiative. More information is available at www.inovio.com.
* * *
This press release contains certain forward-looking statements relating to our business,
including our plans to develop electroporation-based drug and gene delivery technologies and DNA
vaccines and our capital resources. Actual events or results may differ from the expectations set
forth herein as a result of a number of factors, including uncertainties inherent in pre-clinical
studies, clinical trials and product development programs (including, but not limited to, the fact
that pre-clinical and clinical results referenced in this release may not be indicative of results
achievable in other trials or for other indications, that the studies or trials may not be
successful or achieve the results desired, that results from one study may not necessarily be
reflected or supported by the results of other similar studies and that results from an animal
study may not be indicative of results achievable in human studies), the availability of funding to
support continuing research and studies in an effort to prove safety and efficacy of
electroporation technology as a delivery mechanism or develop viable DNA vaccines, the adequacy of
our capital resources, the availability or potential availability of alternative therapies or
treatments for the conditions targeted by the company or its collaborators, including alternatives
that may be more efficacious or cost-effective than any therapy or treatment that the company and
its collaborators hope to develop, evaluation of potential opportunities, issues involving product
liability, issues involving patents and whether they or licenses to them will provide the company
with meaningful protection from others using the covered technologies, whether such proprietary
rights are enforceable or defensible or infringe or allegedly infringe on rights of others or can
withstand claims of invalidity and whether the company can finance or devote other significant
resources that may be necessary to prosecute, protect or defend them, the level of corporate
expenditures, assessments of the companys technology by potential corporate or other partners or
collaborators, capital market conditions, our ability to successfully integrate Inovio and VGX
Pharmaceuticals, the impact of government healthcare proposals and other factors set forth in our
Annual Report on Form 10-K for the year ended December 31, 2009, our Form 10-Q for the nine months
ended September 30, 2010, and other regulatory filings from time to time. There can be no assurance
that any product in Inovios pipeline will be successfully developed or manufactured, that final
results of clinical studies will be supportive of regulatory approvals required to market licensed
products, or that any of the forward-looking information provided herein will be proven accurate.