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Drug

Pertussis Vaccine

Approved · EMA
Emerging researchLate-stage development

Also known as Bordetella pertussis, Pertussis Vaccine, Whole Cell (Adsorbed), pertussis, Pertussis vaccines.

1
Research papers
1
Regulatory events
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this drug.

Approval: VacPertagen (EMA)

Regulatory2026-01-09EMA

Recent increase in infant pertussis cases in Europe and the critical importance of antenatal immunizations: We must do better…now.

Research2024-07-02International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases

Profile

Identifiers & mechanism

Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.

Canonical name
Pertussis Vaccine
Aliases & brands
Bordetella pertussisPertussis Vaccine, Whole Cell (Adsorbed)pertussisPertussis vaccines
RxNorm CUI
8080
ChEMBL ID
CHEMBL2109219
ATC codes
J07AJ52J07AJ02
UNII
2QNL82089R
Regulatory jurisdictions
ema

Regulatory timeline

1 event

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.

Earliest approval
2026-01-09
Latest approval
2026-01-09
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
2026-01-09Approval
Approval: VacPertagen (EMA)
Indication: VacPertagen is indicated for: - booster immunisation against pertussis of individuals 12 years of age and older,- passive protection against pertussis in early infancyShow full indication

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.

Evidence ↗

Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.

Clinical trials

1 trials

The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.

Development programme
CLINICALTRIALS.GOV · LIVE REGISTRY
1
registered trials across all phases
LATEST COMPLETION 2016
1
Late-stage (III+)
1
Completed
PHASE DISTRIBUTIONn = 1
Phase 41

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

1 papers

Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.

Most influential

Recent increase in infant pertussis cases in Europe and the critical importance of antenatal immunizations: We must do better…now.

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2024 · 35 cites
Recent papers

Recent increase in infant pertussis cases in Europe and the critical importance of antenatal immunizations: We must do better…now.

International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2024 · 35 cites
Major research themes4
Bordetella pertussis1COVID-191Pertussis Vaccine1Whooping Cough1
Journals, researchers & institutions
Top journals
  • International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases1
Leading researchers
  • Amirthalingam G1
  • Campbell H1
  • Khalil A1
  • Ladhani SN1
  • Samara A1
Leading institutions
free-text, unnormalised
  • Karolinska Institute1
  • St George's Hospital1
  • UK; Paediatric Infectious Diseases Research Group and Vaccine Institute1
References & data sources
  • 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.