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Drug

Eptifibatide

Approved · EMA
Emerging researchLate-stage development

Also known as Integrilin, Eptifibatida.

2
Research papers
1
Active clinical trials
2
Regulatory events
Latest activity
beta

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

Profile

Identifiers & mechanism

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

Canonical name
Eptifibatide
Aliases & brands
IntegrilinEptifibatida
RxNorm CUI
75635
ChEMBL ID
CHEMBL1174
UNII
NA8320J834
Regulatory jurisdictions
ema

Regulatory timeline

2 events

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
2016-01-11
Latest approval
2016-01-11
Authorities
EMA
Total events
2
emaEuropean Medicines Agency· 2 events
2026-01-01Market withdrawalMarket
Market withdrawal: Integrilin (EMA)
Indication: Integrilin is intended for use with acetylsalicylic acid and unfractionated heparin. Integrilin is indicated for the prevention of early myocardial infarction in patientsShow full indication

Integrilin is intended for use with acetylsalicylic acid and unfractionated heparin. Integrilin is indicated for the prevention of early myocardial infarction in patients presenting with unstable angina or non-Q-wave myocardial infarction with the last episode of chest pain occurring within 24 hours and with ECG changes and / or elevated cardiac enzymes. Patients most likely to benefit from Integrilin treatment are those at high risk of developing myocardial infarction within the first 3-4 days after onset of acute angina symptoms including for instance those that are likely to undergo an early percutaneous transluminal coronary angioplasty (PTCA).

Evidence ↗
2016-01-11Approval
Approval: Eptifibatide Accord (EMA)
Indication: Eptifibatide Accord is intended for use with acetylsalicylic acid and unfractionated heparin. Eptifibatide Accord is indicated for the prevention of early myocardial infarction inShow full indication

Eptifibatide Accord is intended for use with acetylsalicylic acid and unfractionated heparin. Eptifibatide Accord is indicated for the prevention of early myocardial infarction in adults presenting with unstable angina or non-Q-wave myocardial infarction, with the last episode of chest pain occurring within 24 hours and with electrocardiogram (ECG) changes and/or elevated cardiac enzymes. Patients most likely to benefit from Eptifibatide Accord treatment are those at high risk of developing myocardial infarction within the first 3-4 days after onset of acute angina symptoms including for instance those that are likely to undergo an early PTCA (Percutaneous Transluminal Coronary Angioplasty).

Evidence ↗

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

Clinical trials

22 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
22
registered trials across all phases
LATEST COMPLETION 2024
1
Active studies
1
Recruiting
11
Late-stage (III+)
15
Completed
6
Discontinued
PHASE DISTRIBUTIONn = 22
Phase 1 / 22Phase 29Phase 37Phase 44

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

2 papers

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

Publications over time
20092015
Major research themes2
Angioplasty, Balloon, Coronary1Stents1
Journals, researchers & institutions
Top journals
  • Journal of the American College of Cardiology1
  • Stroke1
Leading researchers
  • Adeoye O1
  • Aymong E1
  • Broderick JP1
  • Buller CE1
  • Carere RG1
  • Demel S1
  • Densem C1
  • Eckerle B1
Leading institutions
free-text, unnormalised
  • From the University of Cincinnati Neuroscience Institute1
  • Vancouver General Hospital1
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.