Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
MVA-HBV is a therapeutic vaccine candidate designed to treat chronic hepatitis B infection. It utilizes a modified vaccinia Ankara (MVA) viral vector engineered to express hepatitis B virus (HBV) antigens, specifically the core antigen (HBc) and surface antigen (HBs), separated by a self-cleaving 2A peptide sequence. The vaccine is part of heterologous prime/boost regimens, where it serves as the "boost" following priming with protein-based HBV vaccines. Its mechanism involves stimulating both humoral and cellular immune responses against HBV, aiming to reduce levels of hepatitis B surface antigen in the blood and enhance immune-mediated clearance of infected cells. The vaccine does not replicate in human cells due to its highly attenuated nature, improving its safety profile[1][2][5]. MVA-HBV is being developed for patients with chronic hepatitis B who are already on nucleos(t)ide analog therapy but have not achieved functional cure.
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-HBV.