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Drug

Ticagrelor

Approved · EMA
ClassPurinergic receptor P2Y12 negative allosteric modulatorEmerging researchLate-stage developmentRising momentum

Also known as Brilinta, Brilinta (ticagrelor), (1S,2S,3R,5S)-3-(7-((1R,2S)-2-(3,4-Difluorophenyl)cyclopropylamino)-5-(propylthio)-3H-(1,2,3)triazolo(4,5-d)pyrimidin-3-yl)-5-(2-hydroxyethoxy)cyclopentane-1,2-diol.

4
Research papers
13
Active clinical trials
P2Y purinoceptor 12
Primary target
1
Regulatory events
Latest activity
beta

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

Personalizing Post Surgical Thromboprophylaxis for Patients With Peripheral Artery Disease

Clinical trial2026-05-29Results expected Q2 2027 · ClinicalTrials.gov

A Genotype-Guided Strategy for Oral P2Y<sub>12</sub> Inhibitors in Primary PCI.

Research2019-09-03The New England journal of medicine

Ticagrelor or Prasugrel in Patients with Acute Coronary Syndromes.

Research2019-09-01The New England journal of medicine

Prehospital ticagrelor in ST-segment elevation myocardial infarction.

Research2014-09-01The New England journal of medicine

Approval: Brilique (EMA)

Regulatory2010-12-03EMA

Profile

Identifiers & mechanism

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

Canonical name
Ticagrelor
Aliases & brands
BrilintaBrilinta (ticagrelor)(1S,2S,3R,5S)-3-(7-((1R,2S)-2-(3,4-Difluorophenyl)cyclopropylamino)-5-(propylthio)-3H-(1,2,3)triazolo(4,5-d)pyrimidin-3-yl)-5-(2-hydroxyethoxy)cyclopentane-1,2-diol
RxNorm CUI
1116632
ChEMBL ID
CHEMBL398435
ATC codes
B01AC24
UNII
GLH0314RVC
Primary mechanism
Purinergic receptor P2Y12 negative allosteric modulator
Regulatory jurisdictions
ema

Pharmacology & targets

1 target

Known molecular targets and mechanisms supported by curated pharmacology databases.

P2Y purinoceptor 12
P2RY12 · Q9H244
NEGATIVE ALLOSTERIC MODULATORPurinergic receptor P2Y12 negative allosteric modulator

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
2010-12-03
Latest approval
2010-12-03
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
2010-12-03Approval
Approval: Brilique (EMA)
Indication: Brilique, co administered with acetylsalicylic acid (ASA), is indicated for the prevention of atherothrombotic events in adult patients with acute coronary syndromes (ACS) or aShow full indication

Brilique, co administered with acetylsalicylic acid (ASA), is indicated for the prevention of atherothrombotic events in adult patients with acute coronary syndromes (ACS) or a history of myocardial infarction (MI) and a high risk of developing an atherothrombotic event Brilique, co-administered with acetyl salicylic acid (ASA), is indicated for the prevention of atherothrombotic events in adult patients with a history of myocardial infarction (MI occurred at least one year ago) and a high risk of developing an atherothrombotic event.

Evidence ↗

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

Clinical trials

184 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
184
registered trials across all phases
LATEST COMPLETION 2025
13
Active studies
12
Recruiting
151
Late-stage (III+)
112
Completed
59
Discontinued
PHASE DISTRIBUTIONn = 184
Early Phase 11Phase 111Phase 1 / 24Phase 217Phase 2 / 36Phase 339Phase 493Phase N / A13

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

4 papers

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

Publications over time
20142020
Major research themes3
Emergency Medical Services1Genotype1Percutaneous Coronary Intervention1
Journals, researchers & institutions
Top journals
  • The New England journal of medicine3
  • JAMA1
Leading researchers
  • Hamm CW2
  • Ahn CM1
  • Akin I1
  • Allali A1
  • Angiolillo DJ1
  • Antoniucci D1
  • Asselbergs FW1
  • Baradat C1
Leading institutions
free-text, unnormalised
  • and Technische Universität München (S.S.1
  • Dankook University Hospital1
  • Gangnam Severance Hospital1
  • Gangneung Asan Hospital1
  • Kangwon National University School of Medicine1
  • Myongji Hospital1

Related diseases

3 conditions

Regulator-approved indications and conditions co-mentioned with this drug across the research literature. Number shows shared papers.

Related drugs

5 matches

Drugs sharing diseases, protein targets and literature with this one. Ranked by graph evidence (shared targets + diseases weighted above co-mentions).

Acts on the same molecular target as Ticagrelor, with 6 overlapping disease areas.

Shared target6 shared diseases2 shared papers

Studied across 6 of the same disease areas as Ticagrelor in the shared literature.

6 shared diseases1 shared paper

Studied across 4 of the same disease areas as Ticagrelor in the shared literature.

4 shared diseases1 shared paper

Studied across 4 of the same disease areas as Ticagrelor in the shared literature.

4 shared diseases1 shared paper

Studied across 3 of the same disease areas as Ticagrelor in the shared literature.

3 shared diseases1 shared paper
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.