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GeoVax Labs, Inc. Second Quarter Financial Results and Operational Update
Date:8/19/2007

dose (1/10th of the vaccine dose)

vaccination program. Preliminary results from this blinded trial

demonstrated excellent vaccine safety and positive anti-HIV-1 immune

responses to the vaccine in 9 of 11 participants where 9 people

received GeoVax HIV/AIDS vaccines and 2 received placebos. All trial

participants were normal, healthy individuals. Final results will be

compiled for later public release. The 2nd of four trials, initiated

September 2006, is designed to evaluate results from full dose a

administration of GeoVax HIV/AIDS vaccines. Recent data indicates

excellent safety in this full dose trial with immune response data soon

to be available.

* In June and July, GeoVax announced it engaged Althea Technologies,

Inc., and BioReliance Corporation, as contract manufacturers for its

HIV-1 DNA and HIV-1 MVA (AIDS) vaccines. These vaccines will be

utilized in GeoVax's advanced Phase 2 clinical trials planned for early

2008. GeoVax HIV/AIDS vaccines are designed to prevent development of

Acquired Immunodeficiency Disease (AIDS) caused by the virus known as

HIV-1 by vaccinating individuals prior to AIDS virus infection. The

vaccine regimen employs a two-vaccine "prime-boost strategy." Trial

participants will be administered GeoVax HIV-1 DNA vaccine which

"primes" the immune system followed by GeoVax's HIV-1 MVA (Modified

Vaccinia Virus) boost. Both vaccines deliver over 50% of the AIDS virus

components but can not cause AIDS. Safety and immunological results

from earlier as well as ongoing human trials are very encouraging thus

supporting planned acceleration of large scale Phase 2 clinical

studies.

* In April, GeoVax announced an extension of a research license signed

4/2005 with Vivalis (Nantes, France) to evaluate Vivalis' EBx
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SOURCE GeoVax Labs, Inc.

Copyright©2007 PR Newswire.

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