drugset / Trial / NCT00001072

A Phase I Safety and Immunogenicity Trial of Live Recombinant Canarypox ALVAC-HIV vCP300 and HIV-1 SF-2 rgp120 in HIV-1 Uninfected Adult Volunteers

NCT00001072

Double-blindPrevention

Summary

To evaluate, in HIV-negative volunteers, the safety and immunogenicity of ALVAC-HIV MN120TMGNP (vCP300) followed by or combined with boosting using rgp120/HIV-1SF2. To compare ALVAC-HIV vCP300 with ALVAC-RG rabies glycoprotein (vCP65) as a control. To evaluate an accelerated immunization schedule at 0, 1, 3, and 6 months versus 0, 1, 6, and 9 months. The combination of a live recombinant primer followed by a subunit boost has the potential to induce not only cytotoxic T lymphocytes but also neutralizing antibody.

Timeline

Start
Primary completion
Completion
1999-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject ALVAC-HIV MN120TMGNP Unknown
Subject ALVAC-RG Rabies Glycoprotein Vaccine
Subject rgp120/HIV-1 SF-2 Unknown