Pertussis Vaccine
Approved · EMAAlso known as Bordetella pertussis, Pertussis Vaccine, Whole Cell (Adsorbed), pertussis, Pertussis vaccines.
Recent clinical, regulatory, research and industry developments relating to this drug.
Impact of Pertussis Vaccination in Pregnancy on Maternal Protection Offered to Young Infants
Profile
Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.
Regulatory timeline
The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.
Indication: VacPertagen is indicated for: - booster immunisation against pertussis of individuals 12 years of age and older,- passive protection against pertussis in early infancy… Show full indicationShow less
VacPertagen is indicated for: - booster immunisation against pertussis of individuals 12 years of age and older,- passive protection against pertussis in early infancy following maternal immunisation during pregnancy.
Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.
Clinical trials
The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.
Late-stage studies
Phase III+ trials still open or recently active — where late-stage evidence is being generated.
Recent completions
Trials that read out recently, adding to the completed evidence base.
Research activity
Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.
Major research themes4
Journals, researchers & institutions
- International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases1
- Amirthalingam G1
- Campbell H1
- Khalil A1
- Ladhani SN1
- Samara A1
- Karolinska Institute1
- St George's Hospital1
- UK; Paediatric Infectious Diseases Research Group and Vaccine Institute1
- RxNorm (U.S. National Library of Medicine) — drug identity
- ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
- Europe PMC — research literature
- ClinicalTrials.gov — clinical trials
- Regulatory event sources are credited in the Regulatory Timeline above.