Full Press Release Details
| Contact: | ||
| At The Company: | ||
| Robert McNally | ||
| 678.384.7220 or rmcnally@geovax.com | ||
| At Financial Relations Board: | ||
| Leslie Loyet | ||
| Investor Relations | ||
| 312.640.6672 or lloyet@mww.com | ||
| Nikki Snodgrass | ||
| Media Relations | ||
| 312.640.6732 or nsnodgrass@mww.com |
MONDAY, MARCH 1, 2010
GEOVAX LABS, INC. REPORTS FOURTH QUARTER AND
YEAR END 2009 FINANCIAL RESULTS
Submits Therapeutic Vaccine IND and Awaits FDA Response
ATLANTA, GA, March 1, 2010 GeoVax Labs, Inc. (OTC BB: GOVX), an Atlanta-based biotechnology
company focused on development of HIV/AIDS vaccines, today announced its financial results for the
fourth quarter and year ended December 31, 2009.
GeoVax reported a net loss of $843,285 for the fourth quarter ended December 31, 2009, as compared
to a net loss of $1,039,217 for the comparable period in 2008. For the full year of 2009, the
Company reported a net loss of $3,284,252 as compared to a net loss of $3,728,187 in 2008. Grant
revenues were $3,668,195 and $2,910,170 for the years ended December 31, 2009 and 2008,
respectively. As of December 31, 2009, the Company reported cash balances totaling $3,515,784.
GeoVax s operating results fluctuate due to the timing of activities and related costs associated
with its vaccine research and development activities. Summarized financial information is
attached. Further information concerning the Company s financial position and results of operations
are included in its Annual Report on Form 10-K, expected to be filed with the Securities and
Exchange Commission on or before March 12, 2010.
This past year we continued our work toward the advancement of clinical trials, as well as
increasing the awareness of our potential vaccine solutions for treating and preventing HIV/AIDS.
We are encouraged with our progress on both of these fronts, stated Robert T. McNally, Ph.D.,
president and chief executive officer. He continued, Our technology was further supported by the
September 2009 success of a Thailand-based Phase 3 trial for an HIV/AIDS preventative vaccine
candidate owned by Sanofi-Aventis and Global Solutions for Infectious Disease, which for the first
time elicited both antibody and T cells. Our vaccine compares favorably in that it generates higher
frequencies of T cells and better quality antibody. We think that the GeoVax vaccine has the
potential to deliver a higher success rate than the 30 percent achieved in the trial in Thailand.
This disease has infected about one million people in this country alone and it s our aim to be
part of the solution. We have two vaccine clinical programs. One is for the prevention of the
disease for those who are not
infected, whereas the second is a therapeutic, designed to help those already infected with
HIV-1. Both of our vaccines are based on the same technology and both have demonstrated encouraging
results in non-human primates, he continued.
Preventative Vaccine Trial Phase 2a
The Company s preventative vaccine is in a Phase 2a trial, designated HVTN-205, that is being
conducted by the HIV Vaccine Trials Network (HVTN). The HVTN, funded by the NIH, is the largest
worldwide clinical trials network dedicated to the development and testing of HIV/AIDS vaccines.
Enrollment for this trial began in February 2009. The trial will include a total of 225 volunteers
(150 vaccine recipients and 75 placebo recipients) and take place at 13 HVTN sites: 11 in North
America and two in South America.
Dr. Harriet Robinson, chief scientific officer and developer of the vaccine, stated, We are
currently enrolling in the HVTN Peru sites, which took longer to get fully enrolled than the U.S.
sites, due to the need for Peruvian review of the protocol. The trial is primarily a safety trial
and appears to be performing as expected.
Therapeutic Vaccine Trial IND Submitted to FDA
The protocol for the Phase 1 clinical trial, conceived with collaboration from ARCA (AIDS Research
Consortium of Atlanta), will carefully monitor safety while evaluating the ability for the vaccine
to elicit protective immune responses in vaccinated participants. The proposed trial is based on
the achievement of excellent post vaccine viral control in animal studies conducted in recently
infected non-human primates at the Yerkes National Primate Research Center, affiliated with Emory
GeoVax completed a pre-Investigational New Drug (IND) meeting with the U.S. Food and Drug
Administration (FDA) for its therapeutic trial in December 2009. The clinical path for this
non-blinded trial is expected to have a much shorter duration than the program for the development
of a preventative vaccine. The Company recently submitted its Investigational New Drug application
to the FDA for the therapeutic trial. Following receipt of the IND, the FDA has 30 days to respond.
After that time, if there are no concerns from the FDA the Company may begin the trial.
Adding Resources to Support Growth
We are looking forward to continued progress in 2010. We moved to a larger facility in November
2009 to accommodate our expanding program and future anticipated higher levels of activity, stated
Dr. McNally. While we are adequately capitalized through 2010, thanks in part to $4.7 million in
grant funding from the NIH during 2009, we are evaluating new funding opportunities to support our
About GeoVax Labs, Inc.
GeoVax Labs, Inc. is a biotechnology company, established to develop, manufacture, license and
commercialize human vaccines for diseases caused by HIV-1 and other infectious agents. GeoVax s
AIDS vaccine technology is the subject of 55 issued or filed patent applications in the U.S. and
other countries. GeoVax AIDS vaccines are designed for use in uninfected people to prevent
acquisition of HIV-1 and limit the progression to AIDS should a person become infected. GeoVax AIDS
vaccines also may be effective as a therapeutic treatment (for people already infected with the
AIDS is an epidemic that can affect anyone, regardless of race, gender, age or sexual orientation.
33 million people are currently infected globally and it is estimated that there will be 2.5
million new infections this year. Since the beginning of the epidemic, over a million people in
the U.S. have contracted the virus. Every 9 1/2 minutes, someone in the U.S. is infected with AIDS.
Globally, HIV is the top killer among women of reproductive age.
HIV is a worldwide disease with different subtypes (or clades) of the virus predominating in
different regions of the world. Clade B is the predominant subtype in North America. Globally,
most infections involve subtypes AG, B, and C. In 2008, antiretroviral treatment in low and middle
income countries was restricted to about 3 million people. In the United States, about 50% of those
who are infected are estimated to be on drug treatment.
Safe Harbor Statement
All statements in this news release, not statements of historical fact, are forward-looking
statements. These statements are based on expectations and assumptions on the date of this press
release and are subject to numerous risks and uncertainties which could cause actual results to
differ materially from those described in the forward-looking statements. Risks and uncertainties
include, but are not limited to, whether: GeoVax can develop and manufacture these vaccines with
the desired characteristics in a timely manner, GeoVax s vaccines will be safe for human use,
GeoVax s vaccines will effectively prevent AIDS in humans, vaccines will receive regulatory
approvals necessary to be licensed and marketed, GeoVax raises required capital to complete vaccine
development, there is development of competitive products that may be more effective or easier to
use than GeoVax s products, and other factors over which GeoVax has no control. GeoVax assumes no
obligation to update these forward-looking statements, and does not intend to do so. Certain
matters discussed in this news release are forward-looking statements involving certain risks and
uncertainties including, without limitation, risks detailed in the Company s Securities and
Exchange Commission filings and reports.
FINANCIAL TABLES FOLLOW
Statements of Operations Data
(amounts in thousands, except per share data)
| Three Months Ended | Year Ended | |||||||||||||||
| December 31, | December 31, | |||||||||||||||
| 2009 | 2008 | 2009 | 2008 | |||||||||||||
| Grant Revenue | $ | 397 | $ | 612 | $ | 3,668 | $ | 2,910 | ||||||||
| Operating expenses: | ||||||||||||||||
| Research and development | 538 | 1,016 | 4,068 | 3,741 | ||||||||||||
| General and administrative | 711 | 648 | 2,915 | 2,970 | ||||||||||||
| 1,249 | 1,664 | 6,983 | 6,711 | |||||||||||||
| Loss from operations | (852 | ) | (1,052 | ) | (3,315 | ) | (3,801 | ) | ||||||||
| Interest income | 9 | 13 | 31 | 73 | ||||||||||||
| Net loss | $ | (843 | ) | $ | (1,039 | ) | $ | (3,284 | ) | $ | (3,728 | ) | ||||
| Net loss per common share | $ | (0.00 | ) | $ | (0.00 | ) | $ | (0.00 | ) | $ | (0.01 | ) | ||||
| Weighted averages shares outstanding | 780,410 | 746,067 | 759,564 | 740,143 |
(amounts in thousands)
| December 31, | ||||||||
| 2009 | 2008 | |||||||
| Cash and cash equivalents | $ | 3,516 | $ | 2,191 | ||||
| Working capital | 3,309 | 2,455 | ||||||
| Total assets | 4,316 | 3,056 | ||||||
| Deficit accumulated during the development stage | (17,538 | ) | (14,254 | ) | ||||
| Total stockholders equity | 3,744 | 2,710 |
* * * * * * * * * * * * * * *