Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Pertagen is a recombinant monovalent acellular pertussis (aP) vaccine developed by BioNet-Asia in collaboration with Mahidol University. It is specifically designed for active immunization against *Bordetella pertussis* in individuals aged 11 years and older. Unlike traditional acellular vaccines that rely on chemical detoxification (e.g., using formaldehyde), Pertagen contains a genetically inactivated pertussis toxin (PTgen) and filamentous hemagglutinin (FHA). This genetic inactivation preserves the natural conformational epitopes of the toxin, which is intended to enhance the induction of protective neutralizing antibodies. Licensed in Thailand in 2016, Pertagen was the first recombinant acellular pertussis vaccine to reach the market. It is currently being evaluated in Phase IV studies to assess long-term antibody persistence and the efficacy of decennial booster doses in adults.
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 Pertagen.