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IndexedBuilt automatically from public databases on 2026-09-30. Not yet hand-reviewed by PLOBT.How this works →

Eptifibatide

FDA approved · Rx

Glycoprotein IIb/IIIa inhibitor

Also known as: Integrilin, Integrelin, Eptifibatida, epifibatide, epifibratide, eptifibatidum

Evidence score
91/ 100
Strong evidence

Strong, human-grade evidence

  • Regulatory standing. FDA-approved prescription medicine
  • Human trials. Backed by controlled human studies
  • Registered human trials. 35 registered studies on ClinicalTrials.gov, most advanced Phase 4
  • 2 cited sources. Includes primary / regulatory sources

Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.

What it is

Eptifibatide is a synthetic cyclic heptapeptide, sold originally as Integrilin, that is given intravenously in hospital settings. It blocks the glycoprotein IIb/IIIa receptor on platelets, which prevents fibrinogen from linking platelets together and so reduces clot formation.

What the evidence shows

Automatic summaryHuman trials

It is FDA approved for patients with acute coronary syndrome and for those undergoing percutaneous coronary intervention, supported by large randomized trials and over 1,100 published papers. Bleeding is its main known risk, and its role has narrowed as newer antiplatelet drugs have become standard.

Key facts

Molecular formula
C35H49N11O9S2
Molecular weight
832 g/mol
FDA approval
Confirmed on openFDA

Registered human trials

Published literature

Sources

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