Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
VII3a-IB is an investigational inactivated, trivalent influenza vaccine adjuvanted with IB160, developed by Instituto Butantan in Brazil. The adjuvant, IB160, is a squalene-based oil-in-water emulsion (composed of squalene, Span 85, and Tween 80 in citrate buffer) similar to MF59®, developed with technical support from the Infectious Disease Research Institute (IDRI) and supported by the World Health Organization (WHO) and BARDA. The vaccine targets influenza virus hemagglutinin antigens to elicit a humoral immune response, specifically measured by hemagglutination inhibition titers. It is currently in Phase III clinical development in Brazil, where it is being compared to a high-dose inactivated trivalent influenza vaccine (VII-HD) for non-inferiority in adults aged 60 years and older.
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 VII3a-IB.