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

Bivalirudin

FDA approved · Rx

Direct thrombin inhibitor

Also known as: Angiomax, bivalirudina, bivalirudine, bivalirudinum, BG-8967, BG8967, Hirulog-1, Angiomax RTU

Evidence score
95/ 100
Strong evidence

Strong, human-grade evidence

  • Regulatory standing. FDA-approved prescription medicine
  • Human trials. Backed by controlled human studies
  • Registered human trials. 92 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

Bivalirudin is a synthetic 20-amino-acid peptide modeled on hirudin, the anticoagulant found in medicinal leech saliva. It binds directly and reversibly to thrombin, blocking its role in forming blood clots, and is given intravenously in hospital settings.

What the evidence shows

Automatic summaryHuman trials

Bivalirudin is FDA-approved for use as an anticoagulant in patients undergoing percutaneous coronary intervention (PCI), including those with or at risk of heparin-induced thrombocytopenia. It has a large human evidence base, with about 92 registered trials reaching Phase 4 and nearly 2,000 published papers, though its comparative benefits versus heparin in some settings remain debated.

Key facts

Molecular formula
C98H138N24O33
Molecular weight
2180.3 g/mol
FDA approval
Confirmed on openFDA

Registered human trials

Published literature

Sources

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