Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Diphtheria, tetanus, and acellular pertussis vaccine + hepatitis B vaccine** is a combination vaccine, often formulated as a pentavalent or hexavalent product (e.g., including inactivated poliovirus and sometimes Haemophilus influenzae type b conjugate), designed for primary immunization of infants against diphtheria (caused by Corynebacterium diphtheriae toxoid), tetanus (Clostridium tetani toxoid), pertussis (acellular components targeting pertussis toxin, filamentous hemagglutinin, and pertactin), and hepatitis B (recombinant HBsAg). It induces protective antibody responses, with seroprotection rates typically exceeding 95-100% post-primary series and booster doses for all components, as demonstrated in clinical trials administered at 2, 4, and 6 months. Developed by GlaxoSmithKline (Pediarix) and Merck/Sanofi Pasteur (Vaxelis), it is administered intramuscularly starting at 6 weeks of age in HBsAg-negative mothers' infants, contributing to high vaccination coverage and disease control, with a well-established safety profile from over a decade of post-marketing data.[1][2][3][6][7]
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 diphtheria, tetanus, and acellular pertussis vaccine + hepatitis B vaccine.