drugset / Trial / NCT00095576

Investigation of V520 in an HIV Vaccine Proof-of-Concept Study (V520-023)

NCT00095576 ↗

RandomizedParallel-groupDouble-blindPrevention

Summary

This study will test the safety and efficacy of an investigational Human Immunodeficiency Virus (HIV) vaccine. Efficacy will be measured by either prevention of HIV infection or control of HIV viral load in subjects who become HIV infected. On September 18, 2007 the Protocol V520-023 DSMB (Data \& Safety Monitoring Board) reviewed data from a planned interim analysis. These data demonstrated that the investigational vaccine candidate was not effective, and all vaccinations in the study were halted. Participants were encouraged to continue to come to the clinic for scheduled visits and ongoing risk reduction counseling since the vaccine was not effective.

Timeline

Start
2004-11
Primary completion
2007-09
Completion
2009-09

Outcome

Missed primary endpoint

paper There was no overall effect of vaccine on mean log(10) viral load (estimated difference between groups, -0.11; P = .47). PMID 21343146 ↗

paper The adjusted vaccinees vs placebo recipients hazard ratio (HR) for all follow-up time was 1.40 (95% confidence interval [CI], 1.03-1.92; P= .03). PMID 22561365 ↗

paper At the first interim analysis, nonefficacy criteria were met. PMID 22561365 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject MRKAd5 HIV-1 gag/pol/nef Vaccine 1.5e+10 vg Intramuscular

Indications