drugset / Trial / NCT00000813

A Phase I Safety and Immunogenicity Trial of Live Recombinant Canarypox-gp160 MN (ALVAC vCP125, HIV-1 gp160 MN) in HIV-1 Uninfected Adult Volunteers

NCT00000813

Double-blindPrevention

Summary

Part A: To evaluate the safety and immunogenicity of ALVAC vCP125 HIV-1 gp160 MN live canarypox recombinant vaccine (ALVAC gp160 MN) versus a recombinant canarypox expressing the rabies glycoprotein (ALVAC rabies glycoprotein) as a control in healthy, HIV-1 uninfected adult volunteers. Part B: To evaluate the schedule of two immunizations with ALVAC gp160 MN for optimal immunogenicity. Amendment: 12/22/93: To determine whether ALVAC gp160 MN in combination with SF-2 rgp120 subunit protein is capable of generating humoral and cellular immune responses of greater intensity and longer duration than either vaccine administered alone. A canarypox-vectored vaccine (ALVAC) that expresses the gp160 antigen of the HIV-1 MN strain might satisfy many criteria for an affordable HIV vaccine. Per 12/22/93 amendment: Cellular responses have been augmented by the combination of two recombinant vaccines, especially in vaccinia naive individuals.

Timeline

Start
Primary completion
Completion
1995-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject ALVAC-HIV gp160MN Vaccine 1e+06 unknown Intramuscular
Subject ALVAC-HIV gp160MN Vaccine 1e+07 unknown Intramuscular
Subject ALVAC-RG Rabies Glycoprotein Vaccine Intramuscular
Subject rgp120/HIV-1 SF-2 Protein / enzyme biologic