GAITHERSBURG, Md.--(BUSINESS WIRE)--GenVec, Inc. (Nasdaq:GNVC) announced that results from multiple ongoing clinical trials utilizing its adenovector vaccine technologies were presented yesterday at the AIDS Vaccine 2007 Conference taking place in Seattle, Washington this week. The trials, which are investigating a DNA prime- adenoviral vector boost strategy, incorporate a multiclade rAd5 HIV- 1 vaccine developed by GenVec in collaboration with the Vaccine Research Center (“VRC”), National Institute of Allergy and Infectious Diseases, National Institutes of Health (“NIH”).
Dr. Richard Koup of the VRC, delivered an oral presentation, “Update on Safety and Immunogenicity of VRC Products,” summarizing data from several ongoing studies sponsored by the NIH’s HIV Vaccine Trials Network (“HTVN”), the International AIDS Vaccine Initiative (“IAVI”) and the U.S. Military HIV Research Program (“USMHRP”) using the DNA prime-boost regimen. Dr. Koup characterized a strong vaccine induced cytotoxic (CD8+) T-cell response targeting HIV-infected cells, confirming the underlying concept of this vaccine. In the TRIAD Phase II trial, immunogenicity was achieved in approximately seventy percent of the vaccinated population. Importantly, the effect of pre-existing Ad5 immunity on immunogenicity of the vaccine appeared to be small. More than ten abstracts, posters, and presentations were presented by the VRC and its collaborators at this conference.
“The Phase 2 trials have generated a tremendous amount of information on clinical application of adenovirus vectors as vaccines. These data strongly support the use of GenVec adenovirus vectors as vaccines for HIV and other diseases,” commented Dr. Rick King, GenVec’s Senior VP of Research.
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