drugset / Trial / NCT02852005

Evaluating the Immunogenicity of the AIDSVAX B/E Vaccine and the MVA/HIV62B Vaccine in Healthy, HIV-1-Uninfected Adults Who Previously Received MVA/HIV62B in DNA/MVA or MVA/MVA Regimens in HVTN 205

NCT02852005 ↗

RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to evaluate the safety, tolerability, and immunogenicity of the AIDSVAX B/E vaccine and the MVA/HIV62B vaccine in healthy, HIV-1-uninfected adults who previously received MVA/HIV62B in DNA/MVA or MVA/MVA vaccine regimens in the HVTN 205 study.

Timeline

Start
2017-01
Primary completion
2018-08-29
Completion
2019-10-29

Drugs

EvaluationDrugModalityDoseRoute
Subject AIDSVAX B/E Vaccine 600 ug/ml Intramuscular
Subject MVA/HIV62B Vaccine 1e+08 unknown Intramuscular