Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The P2-VP8 subunit vaccine is a non-replicating, recombinant protein subunit vaccine developed by PATH for the prevention of rotavirus gastroenteritis. Unlike traditional oral live-attenuated rotavirus vaccines, this candidate is administered parenterally via intramuscular injection, which may improve efficacy in low-income settings where oral vaccines often underperform. The vaccine is composed of a truncated VP8 subunit protein derived from the rotavirus outer capsid spike protein VP4, fused to a universal T-cell epitope (P2) from tetanus toxin to enhance the immune response. It is expressed in Escherichia coli and formulated with an aluminum hydroxide adjuvant (Alhydrogel). The vaccine has been developed in both monovalent (targeting the P[8] genotype) and trivalent (targeting P[4], P[6], and P[8] genotypes) formulations, and clinical trials have demonstrated its safety and immunogenicity in infants and toddlers.
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 P2-VP8 subunit vaccine.