At a glance
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A Phase 1B Clinical Trial to Evaluate the Safety and Immunogenicity of Recombinant Adenoviral Serotype 35 (rAd35) and Serotype 5 (rAd5) HIV-1 Vaccines When Given in Heterologous Prime-Boost Regimens or as a Boost to a Recombinant DNA Vaccine in Healthy, HIV-1-Uninfected Adult Participants With Pre-Existing Immunity to Adenovirus Serotype 5 Infection
In Brief
A Phase 1 clinical trial evaluating VRC-HIVADV027-00-VP, VRC-HIVADV038-00-VP, and 1 other intervention for HIV Infections. Completed, enrolled 17 participants across 7 sites.
Detailed Summary
The purpose of this study is to determine the safety of and immune response to an experimental DNA HIV vaccine followed by boosting with either an experimental adenoviral vector HIV vaccine of serotype 5 or 35 in HIV uninfected adults. This study will also determine the safety of and immune response to an adenoviral vector HIV vaccine of serotype 5 followed by a booster of an adenoviral vector of serotype 35, or vice versa, in HIV uninfected adults.
Study Details
Timeline
Interventions
Adenoviral vector booster vaccine
Adenovirus vector booster vaccine
Experimental, multiclade, multigene HIV DNA vaccine