Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The trivalent rotavirus reassortant vaccine is a live-attenuated oral vaccine developed by the Lanzhou Institute of Biological Products (LIBP) for the prevention of rotavirus-induced gastroenteritis in infants and children. It is an evolution of the monovalent Lanzhou Lamb Rotavirus (LLR) vaccine, utilizing the lamb rotavirus strain (G10P[15]) as a genetic backbone. Through reassortment, the vaccine incorporates human rotavirus VP7 surface proteins from serotypes G2, G3, and G4. This multivalent approach is designed to provide broader protective immunity against the most prevalent circulating rotavirus serotypes in China compared to the original monovalent formulation. The vaccine was approved by the National Medical Products Administration (NMPA) of China to reduce the incidence and severity of diarrhea caused by rotavirus infections.
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 trivalent rotavirus reassortant vaccine.