Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The influenza A (H5N1) virus monovalent vaccine is an inactivated split-virus biologic developed for the prevention of avian influenza (bird flu). It contains hemagglutinin (HA) from the A/Indonesia/05/2005 strain and was evaluated in clinical trials sponsored by the National Institute of Allergy and Infectious Diseases (NIAID). The vaccine is often administered with the AS03 adjuvant, an oil-in-water emulsion containing squalene, DL-α-tocopherol, and polysorbate 80, which is manufactured by GSK. This adjuvanted formulation is designed to enhance immunogenicity and provide broader cross-protection against heterologous H5N1 strains. The vaccine itself has been manufactured by Sanofi Pasteur and GSK for use in NIAID-led systems biology studies.
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 influenza a (h5n1) virus monovalent vaccine-National Institute of Allergy and Infectious Diseases (NIAID)-Influenza A (H5N1).