Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The absorbed acellular diphtheria-tetanus-pertussis (component) combined vaccine is a trivalent vaccine developed by Beijing Zhifei Luzhu Biopharmaceutical. Unlike traditional co-purified DTaP vaccines, this 'component' vaccine (DTaP-cp) is formulated with purified individual antigens, typically including diphtheria toxoid, tetanus toxoid, and specific acellular pertussis antigens such as pertussis toxoid (PT) and filamentous hemagglutinin (FHA), adsorbed onto an aluminum-based adjuvant. It is intended for the active immunization of infants and children against diphtheria, tetanus, and pertussis (whooping cough). As of 2023, the vaccine is undergoing Phase III clinical evaluation in China to assess its safety and immunogenicity in a primary and booster vaccination schedule.
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 absorbed acellular diphtheria-tetanus-pertussis (component) combined vaccine.