Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**TetrAnflu** is a quadrivalent inactivated split-virion influenza vaccine developed by Sinovac Biotech Ltd. for active immunization against influenza A (H1N1 and H3N2) and B (Victoria and Yamagata lineages) virus strains recommended annually by the WHO. Produced via chicken embryo culture, inactivation, purification, and disruption, it induces humoral antibody responses to prevent symptomatic influenza infection, with demonstrated immunogenicity superior to comparators in clinical studies and seroprotection rates up to 99.4%. It features a preservative-free formulation with stringent purity standards exceeding Chinese and European pharmacopeia limits, and has been administered in nearly 100 million doses worldwide, approved in China (including for ages 6 months+), Hong Kong, Bangladesh, and the Dominican Republic.[2][6][9]
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 TetrAnflu.