drugset / Trial / NCT01435135

Study of Late Boost Strategies for HIV-uninfected Participants From Protocol RV 144

NCT01435135

RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to assess safety and tolerability of late boost regimens of AIDSVAX B/E alone, ALVAC-HIV alone, or ALVAC-HIV/AIDSVAX B/E combination in HIV-uninfected participants from RV 144.

Timeline

Start
2012-04
Primary completion
2021-07
Completion
2021-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject AIDSVAX B/E Vaccine 600 ug
Subject ALVAC-HIV Vaccine 1e+06 unknown