Ticagrelor
Approved · EMAAlso 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.
Recent clinical, regulatory, research and industry developments relating to this drug.
Personalizing Post Surgical Thromboprophylaxis for Patients With Peripheral Artery Disease
A Genotype-Guided Strategy for Oral P2Y<sub>12</sub> Inhibitors in Primary PCI.
Ticagrelor or Prasugrel in Patients with Acute Coronary Syndromes.
Prehospital ticagrelor in ST-segment elevation myocardial infarction.
Profile
Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.
Pharmacology & targets
Known molecular targets and mechanisms supported by curated pharmacology databases.
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: 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… Show full indicationShow less
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.
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 themes3
Journals, researchers & institutions
- The New England journal of medicine3
- JAMA1
- Hamm CW2
- Ahn CM1
- Akin I1
- Allali A1
- Angiolillo DJ1
- Antoniucci D1
- Asselbergs FW1
- Baradat C1
- 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
Regulator-approved indications and conditions co-mentioned with this drug across the research literature. Number shows shared papers.
Related drugs
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.
Studied across 6 of the same disease areas as Ticagrelor in the shared literature.
Studied across 4 of the same disease areas as Ticagrelor in the shared literature.
Studied across 4 of the same disease areas as Ticagrelor in the shared literature.
Studied across 3 of the same disease areas as Ticagrelor in the shared literature.
- 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.