Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
MRVAC is a live-attenuated combination vaccine developed for the prevention of measles and rubella. Produced by the Center for Research and Production of Vaccines and Biologicals (POLYVAC) in Vietnam, the vaccine was created using technology transferred from Japan (specifically from Kitasato Daiichi Sankyo Vaccine). It contains the AIK-C strain of the measles virus and the Takahashi strain of the rubella virus, both attenuated to induce a protective immune response without causing disease. Clinical trials, including a Phase III study in Vietnamese volunteers aged 1 to 45 years, have demonstrated that MRVAC is safe and provides immunogenicity non-inferior to established international vaccines like those from the Serum Institute of India. It is a key component of Vietnam's national expanded program on immunization, providing a locally manufactured option for disease control.
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 MRVAC.