Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
MVA.HIVA is a viral vector-based vaccine candidate designed for the prevention of HIV-1 infection. Developed at the University of Oxford and sponsored by the Medical Research Council (MRC), the vaccine utilizes the Modified Vaccinia virus Ankara (MVA) platform, a highly attenuated strain of vaccinia virus. The vaccine construct expresses a consensus HIV-1 clade A immunogen (HIVA), which consists of a consensus clade A Gag p24/p17 sequence linked to a string of cytotoxic T-lymphocyte (CTL) epitopes. These epitopes are derived from the Gag, Pol, Env, and Nef proteins of HIV-1 clade A isolates common in East Africa. MVA.HIVA is engineered to induce robust T-cell mediated immune responses against HIV-1. It has been evaluated in several clinical trials, including the Phase I/II PedVacc 002 study, which assessed its safety and immunogenicity in healthy infants born to HIV-1-infected mothers in Kenya.
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 MVA.HIVA.