drugset / Trial / NCT00001076

A Phase I Safety and Immunogenicity Trial of Live Recombinant Canarypox ALVAC-HIV (vCP205) and HIV-1 SF-2 rgp120 in HIV-1 Uninfected Volunteers to Evaluate Accelerated Vaccine Schedules

NCT00001076

Double-blindPrevention

Summary

To evaluate the safety and immunogenicity of an accelerated schedule of recombinant canarypox vaccine ALVAC-HIV MN120TMG (vCP205) versus control followed by boost with rgp120/HIV-1 SF2 vaccine in HIV-negative volunteers. Frequent injections of ALVAC-HIV vCP205 may result in more rapid induction of cytotoxic T-lymphocytes. This trial will evaluate whether an accelerated vaccination schedule can produce immunological responses comparable to those obtained in other trials of ALVAC-HIV vCP205.

Timeline

Start
Primary completion
Completion
1997-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject ALVAC-HIV MN120TMG Vaccine
Subject ALVAC-RG Rabies Glycoprotein Vaccine
Subject rgp120/HIV-1 SF-2 Unknown