Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This entry refers to the co-administration of Pfizer's **Trumenba** (a bivalent recombinant lipoprotein 2086 vaccine) and a pediatric **hepatitis A vaccine**. Trumenba is designed to prevent invasive disease caused by *Neisseria meningitidis* serogroup B by inducing bactericidal antibodies against factor H binding protein (fHBP), a surface protein that allows the bacteria to evade the host's immune system. The hepatitis A vaccine is an inactivated virus vaccine that provides active immunity against the hepatitis A virus (HAV). This specific co-administration regimen has been evaluated in Phase 2 clinical trials (such as NCT01461980) to assess the safety, tolerability, and immunogenicity of Trumenba when given alongside routine pediatric vaccinations in healthy toddlers aged 12 to 24 months.
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 Trumenba + hepatitis A vaccine.