Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ALVAC-HIV + bivalent gp120 protein is an investigational HIV-1 preventive vaccine regimen consisting of two components used in a prime-boost strategy. The first component, ALVAC-HIV (vCP2438), is a recombinant canarypox viral vector vaccine that expresses HIV-1 env gp120 (subtype C, ZM96.C strain) linked to the gp41 transmembrane sequence, along with gag and protease from the subtype B LAI strain. The second component is a bivalent subtype C gp120 protein boost, combining 100 mcg each of the HIV-1 subtype C gp120 proteins from the TV1.C and 1086.C strains. The regimen is typically adjuvanted with MF59 (a squalene oil-in-water emulsion), alum, or AS01B to enhance immunogenicity. Developed by Sanofi Pasteur in collaboration with the HIV Vaccine Trials Network (HVTN) and NIAID, this regimen specifically targets HIV-1 subtype C, which is prevalent in sub-Saharan Africa. It aims to elicit HIV-specific humoral (binding and neutralizing antibodies) and cellular (CD4+ T-cell) immune responses. While it showed promise in Phase 1/2 trials (HVTN 100), the Phase 2b/3 Uhambo trial (HVTN 702) was stopped early in 2020 due to a lack of efficacy in preventing HIV infection.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on ALVAC-HIV + bivalent gp120 protein.