Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The MF59-adjuvanted quadrivalent influenza vaccine is an inactivated influenza vaccine containing four viral strains (two influenza A and two influenza B) and the MF59 adjuvant, an oil-in-water emulsion of squalene. MF59 enhances the immune response by creating a transient immunocompetent environment at the injection site, recruiting key immune cells, increasing antigen uptake, and promoting more efficient adaptive immune activation, including CD4+ T-cell and B-cell responses. The vaccine is designed for improved immunogenicity and effectiveness, particularly in children and older adults, compared to non-adjuvanted vaccines. Developed and manufactured primarily by Seqirus, it is approved for individuals ≥65 years (Fluad Quadrivalent) and has pending/approved pediatric formulations.
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 MF59-adjuvanted quadrivalent influenza vaccine.