Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is an experimental formulation of Seqirus's MF59-adjuvanted trivalent influenza vaccine (aTIV) designed for the elderly population (65 years and older). It features modified concentrations of both the influenza hemagglutinin antigens and the MF59 adjuvant, typically involving doubled or tripled dosages compared to the standard licensed version (FLUAD). The vaccine contains subunit antigens from two influenza A strains and one influenza B strain. The MF59 adjuvant, an oil-in-water emulsion composed of squalene, polysorbate 80, and sorbitan trioleate, is included to overcome immunosenescence by enhancing the recruitment of antigen-presenting cells and increasing the breadth and magnitude of the antibody response. A Phase 1 dosage-finding study evaluated these modified levels to optimize immunogenicity against seasonal influenza while monitoring for increased local reactogenicity.
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 antigen and adjuvant level modified adjuvanted, trivalent subunit influenza vaccine-Seqirus-influenza.