drugset / Trial / NCT00384787

Safety of and Immune Response to a DNA HIV Vaccine Followed by an Adenoviral Vaccine Boost Given Three Different Ways to HIV Uninfected Adults

NCT00384787

RandomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is to determine the safety of, immune response to, and tolerability of an adenoviral vector HIV vaccine given after a three-dose regimen of a DNA HIV vaccine. The adenoviral vaccine will be given into arm muscle (intramuscularly), between skin layers (intradermally), or under the skin (subcutaneously). NOTE: In October 2007, vaccinations with the adenoviral vaccine, VRC-HIVADV014-00-VP, were discontinued. In December 2007, vaccinations with the DNA vaccine were also discontinued. Participants will be followed for safety and immune responses at regular study visits.

Timeline

Start
2006-11
Primary completion
2008-11
Completion
2012-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject VRC-HIVADV014-00-VP Vaccine Intramuscular
Subject VRC-HIVDNA009-00-VP Vaccine Intramuscular