Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Antigen level modified adjuvanted trivalent subunit influenza vaccine** is an investigational MF59-adjuvanted, inactivated trivalent influenza subunit vaccine formulation developed in the Seqirus seasonal influenza vaccine program. In the completed Phase 1 study NCT02126761, this was the Group 3 antigen-only modified formulation, with the usual aggregate hemagglutinin antigen amount doubled from 45 micrograms to 90 micrograms across the A/H1N1, A/H3N2, and influenza B components while retaining MF59 adjuvantation. It was evaluated for safety and immunogenicity in adults aged 65 years and older and is distinct from the licensed standard-antigen-dose Fluad formulation. ([cdek.pharmacy.purdue.edu](https://cdek.pharmacy.purdue.edu/trial/NCT02126761/))
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 level modified adjuvanted trivalent subunit influenza vaccine.