Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**FluShield** was a Wyeth seasonal injectable **trivalent inactivated split-virion influenza vaccine** used for active immunization against influenza. The documented 1996-1997 formulation contained 15 micrograms of hemagglutinin from each of three strains: A/Texas/36/91 H1N1, A/Wuhan/359/95 H3N2, and B/Beijing/184/93. It induces strain-specific anti-influenza antibody responses against viral hemagglutinin antigens. Wyeth announced cessation of FluShield production in January 2003, before the 2003-2004 influenza season. ([infectioncontroltoday.com](https://www.infectioncontroltoday.com/view/wyeth-ceases-production-its-injectable-influenza-vaccine-and-pneumococcal))
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 FluShield.