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Bivalirudin

Aliases: Angiomax

Last verified: 2026-09-23

Approved drugStrong evidencePeptidesMedium interest

The short version

A 20-aa peptide — direct thrombin inhibitor (hirudin analogue), anticoagulant in PCI.

Identity & type

Molecular type
analog
Origin
A 20-aa peptide — direct thrombin inhibitor (hirudin analogue), anticoagulant in PCI.

Mechanism of action

Bivalently binds thrombin (catalytic site + exosite 1), reversibly.

Dosing & routes

Official / clinical context

Approved drug — indications, dosing and warnings are defined by the official label. IV bolus 0.75 mg/kg + 1.75 mg/kg/h during PCI.

Regulator-approved labeling and published study designs — never a recommendation.

Community-reported practice

IV bolus 0.75 mg/kg + 1.75 mg/kg/h during PCI. Angiomax: an anticoagulant during PCI with lower bleeding risk than heparin; hospital use.

Unverified self-reports. Not medical advice. Not endorsement.

Expected effects (community)

Angiomax: an anticoagulant during PCI with lower bleeding risk than heparin; hospital use.

Protocol — official vs community

Official / label

Angiomax (PCI anticoagulation): 0.75 mg/kg IV bolus followed by 1.75 mg/kg/h infusion during the procedure; post-PCI continuation at 1.75 mg/kg/h for up to 4 h is label-supported in STEMI, with optional reduced-rate infusion beyond.

Duration: Hours — procedure-scoped. Dose-adjust per label in renal impairment; the short half-life (~25 min) makes it effectively self-reversing.

HORIZONS-AMI established its bleeding advantage over heparin plus GP IIb/IIIa in primary PCI. Hospital-only agent; there is no outpatient or community context for a drug whose half-life is measured in minutes.

Community (anecdotal)

Structured protocol data for this entry is coming.

Human evidence

HORIZONS-AMI and later PCI trials.

Preclinical evidence

The preclinical phase was completed and submitted to regulators as part of registration; pharmacology and toxicology details are part of the official label.

Known risks

  • Bleeding (less than heparin+GPI).characterized

Teal: characterized in clinical/labeling contexts. Amber: theoretical or reported outside controlled settings.

Unknowns & evidence gaps

  • Real-world data outside controlled trials

Frequently asked questions

References