Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
PR51 is a hexavalent combination vaccine formulation developed by Merck Sharp & Dohme LLC. It is designed to provide immunity against Haemophilus influenzae type b, Hepatitis B, Diphtheria, Tetanus, Pertussis, and Poliovirus types 1, 2, and 3. The vaccine contains specific antigens, such as PRP-OMPC (for Haemophilus influenzae type b) and HBsAg (for Hepatitis B), along with diphtheria toxoid, tetanus toxoid, a 5-component acellular pertussis vaccine, and inactivated poliovirus types 1, 2, and 3. Different formulations of PR51, varying in the dosage of PRP-OMPC and HBsAg, are being evaluated for their safety, tolerability, and immunogenicity.
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 PR51.