drugset / Trial / NCT00751595

Immunogenicity and Safety Trial of the HIV-1 Tat Vaccine

NCT00751595 ↗

Phase 2 Completed 168 enrolled Barbara Ensoli, MD
RandomizedParallel-groupOpen-labelTreatment

Summary

The study is a randomized, open label, phase II clinical trial directed at evaluating the immunogenicity (as a primary end-point) and the safety (as a secondary end-point), of the recombinant HIV-1 Tat vaccine in HIV-1 infected adult subjects, anti-Tat antibody negative, HAART-treated with chronic suppressed HIV-1 infection, CD4+ T cell counts \>= 200 cells/microliter, levels of plasma viremia \< 50 copies/ml in the last 6 months prior to the screening and without a history of virologic rebound. The immunogenicity of 3 or 5 immunizations of the two different vaccine doses (7.5 and 30 micrograms) of the Tat vaccine has been evaluated.

Timeline

Start
2008-09
Primary completion
2012-06
Completion
2012-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tat protein Vaccine 7.5 ug Other
Subject Tat protein Vaccine 30 ug Other