Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
The two-component acellular pertussis vaccine is an investigational biologic vaccine developed by SmithKline Beecham (now GSK) for the prevention of pertussis (whooping cough). It contains two purified antigens from *Bordetella pertussis*: 25 μg of pertussis toxin (PT) inactivated by glutaraldehyde and formalin, and 25 μg of formalin-treated filamentous hemagglutinin (FHA). Typically formulated as a diphtheria-tetanus-acellular pertussis (DTaP) combination, it was evaluated in large-scale clinical trials in Sweden during the 1990s. Although it demonstrated a protective efficacy of 58.9% against laboratory-confirmed pertussis, it was found to be less effective than five-component acellular vaccines and was never commercialized for clinical use.
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 two-component acellular pertussis vaccine.