Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The RIBSP allantoic split inactivated seasonal influenza vaccine is a trivalent, egg-derived, split-virion vaccine developed by the Research Institute for Biological Safety Problems in Kazakhstan. It contains inactivated influenza virus strains of subtypes A (H1N1pdm09 and H3N2) and type B, standardized to 15 µg of hemagglutinin per strain per 0.5 ml dose. The vaccine is produced using allantoic fluid from embryonated chicken eggs and is notably formulated without adjuvants or preservatives. It is designed to induce protective antibody responses against seasonal influenza by targeting the viral hemagglutinin surface protein. Clinical evaluation has reached Phase II, where it demonstrated safety and immunogenicity comparable to the commercial vaccine Vaxigrip in healthy adults aged 18-60 and over 60 years.
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 RIBSP allantoic split inactivated seasonal influenza vaccine.