U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
Bivalirudin is a synthetic 20 amino acid peptide rationally designed based on structural studies of hirudin, a naturally occurring anticoagulant. Bivalirudin is sold under the brand name Angiomax and is indicated for use as an anticoagulant in patients with unstable angina undergoing percutaneous transluminal coronary angioplasty (PTCA). It is intended for use with aspirin and has been studied only in patients receiving concomitant aspirin. Bivalirudin directly inhibits thrombin by binding simultaneously to its active catalytic site and its substrate recognition site.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P00734|||Q9UCA1
Gene ID: 2147.0
Gene Symbol: F2
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Palliative
ANGIOMAX

Approved Use

Angiomax™ is indicated for use as an anticoagulant in patients with unstable angina undergoing percutaneous transluminal coronary angioplasty (PTCA). Angiomax is intended for use with aspirin and has been studied only in patients receiving concomitant aspirin.

Launch Date

2000
PubMed

PubMed

TitleDatePubMed
Antibodies against lepirudin are polyspecific and recognize epitopes on bivalirudin.
2004-01-15
Comparison of effectiveness and safety of three different antithrombotic regimens (bivalirudin, eptifibatide, and heparin) in preventing myocardial ischemia during percutaneous coronary intervention.
2003-11-01
Bivalirudin provides increasing benefit with decreasing renal function: a meta-analysis of randomized trials.
2003-10-15
Successful use of bivalirudin for cardiopulmonary bypass in a patient with heparin-induced thrombocytopenia.
2003-10
Direct thrombin inhibitors for non-ST-segment elevation acute coronary syndromes: what, when, and where?
2003-10
Argatroban for off-pump coronary artery bypass surgery.
2003-10
Heparin-induced thrombocytopenia: pathophysiology and new treatment options.
2003-09-19
Bivalirudin in percutaneous coronary intervention.
2003-09-15
Heparin-induced thrombocytopenia and cardiac surgery.
2003-08
Contemporary use of antiplatelet therapies in percutaneous coronary interventions.
2003-08
Can bivalirudin and provisional GP IIb/IIIa blockade REPLACE heparin and planned glycoprotein IIb/IIIa blockade during percutaneous coronary intervention?
2003-08
Economic impact of bleeding complications and the role of antithrombotic therapies in percutaneous coronary intervention.
2003-07-15
Current anticoagulant therapy--unmet clinical needs.
2003-07-15
A 24-hour continuous infusion study of bivalirudin in the rat.
2003-07-10
Hirulog-like peptide reduces restenosis and expression of tissue factor and transforming growth factor-beta in carotid artery of atherosclerotic rabbits.
2003-07
Bivalirudin use in off-pump myocardial revascularization in patients with heparin-induced thrombocytopenia [corrected].
2003-07
Bivalirudin in peripheral vascular interventions: a single center experience.
2003-07
Evolving role of bivalirudin in percutaneous coronary interventions; impact of the REPLACE-2 study.
2003-06
Bivalirudin as a foundation anticoagulant in peripheral vascular disease: a safe and feasible alternative for renal and iliac interventions.
2003-06
Correlation of point-of-care ecarin clotting time versus activated clotting time with bivalirudin concentrations.
2003-05-01
Predicting the pharmacology of thrombin inhibitors.
2003-05
Direct thrombin inhibitors.
2003-05
In-hospital complications of peripheral vascular interventions using unfractionated heparin as the primary anticoagulant.
2003-05
An assessment of different filter systems for extracorporeal elimination of bivalirudin: an in vitro study.
2003-05
Management of thrombotic and cardiovascular disorders in the new millenium.
2003-04
Anticoagulation in acute cardiac care in patients with chronic kidney disease.
2003-04
Informed consent during the clinical emergency of acute myocardial infarction (HERO-2 consent substudy): a prospective observational study.
2003-03-15
Safe and efficacious use of bivalirudin for percutaneous coronary intervention with adjunctive platelet glycoprotein IIb/IIIa receptor inhibition.
2003-03-15
Bivalirudin (Angiomax) use during intracoronary brachytherapy may predispose to acute closure.
2003-03
The evolving role of direct thrombin inhibitors in acute coronary syndromes.
2003-02-19
Should bivalirudin replace heparin during percutaneous coronary interventions?
2003-02-19
Bivalirudin and provisional glycoprotein IIb/IIIa blockade compared with heparin and planned glycoprotein IIb/IIIa blockade during percutaneous coronary intervention: REPLACE-2 randomized trial.
2003-02-19
Reversing anticoagulants both old and new.
2003-02-01
Clinician update: direct thrombin inhibitors in acute coronary syndromes.
2003-02
Bivalirudin monitored with the ecarin clotting time for anticoagulation during cardiopulmonary bypass.
2003-02
Alternative methods of anticoagulation for dialysis-dependent patients with heparin-induced thrombocytopenia.
2003-01-22
Favorable outcome with bivalirudin anticoagulation during cardiopulmonary bypass.
2003-01
Effect of non-heparin thrombin antagonists on thrombin generation, platelet function, and clot structure in whole blood.
2003
Direct thrombin inhibitors in cardiac disease.
2003
Anticoagulation with bivalirudin during cardiopulmonary bypass in cardiac surgery.
2002-12
A Bayesian ordinal model for heterogeneity in a multi-centre myocardial infarction clinical trial.
2002-10-30
Gateways to clinical trials.
2002-10
Direct thrombin inhibitors in acute coronary syndromes.
2002-08-10
Decreased platelet reactivity in blood anticoagulated with bivalirudin or enoxaparin compared with unfractionated heparin: implications for coronary intervention.
2002-06
Direct thrombin inhibitors.
2002-05-01
Current developments in antithrombotic therapy: the role of antithrombin agents.
2002
Current anticoagulation options in percutaneous intervention: designing patient-specific strategies.
2002
Optimal treatment and current situation in reperfusion after thrombolysis for acute myocardial infarction.
2002
Development and current applications of thrombin-specific inhibitors.
2001-06
Thrombin-specific inhibition by and slow cleavage of hirulog-1.
1992-05-01
Patents

Sample Use Guides

The recommended dosage of Angiomax (bivalirudin) is an intravenous (IV) bolus dose of 1.0 mg/kg followed by a 4-hour IV infusion at a rate of 2.5 mg/kg/h. After completion of the initial 4-hour infusion, an additional IV infusion of Angiomax may be initiated at a rate of 0.2 mg/kg/h for up to 20 hours if needed.
Route of Administration: Intravenous
Substance Class Protein
Created
by admin
on Tue Apr 01 18:11:06 GMT 2025
Edited
by admin
on Tue Apr 01 18:11:06 GMT 2025
Protein Sub Type
Sequence Type COMPLETE
Record UNII
8631NP8608
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BIVALIRUDIN TRIFLUOROACETATE
USAN  
USAN  
Official Name English
ANGIOMAX
Preferred Name English
ANGIOX
Brand Name English
HIRULOG
Brand Name English
ANGIOMAX RTU
Brand Name English
Bivalirudin trifluoroacetate [WHO-DD]
Common Name English
D-PHENYLALANYL-L-PROLYL-L-ARGINYL-L-PROLYLGLYCYLGLYCYLGLYCYLGLYCYL-L-ASPARAGINYLGLYCYL-L-.ALPHA.-ASPARTYL-L-PHENYLALANYL-L-.ALPHA.-GLUTAMYL-L-.ALPHA.-GLUTAMYL-L-ISOLEUCYL-L-PROLYL-L-.ALPHA.-GLUTAMYL-L-.ALPHA.-GLUTAMYL-L-TYROSYL-L-LEUCINE BIS(2,2,2-TRIFLU
Systematic Name English
BIVALIRUDIN TRIFLUOROACETATE [USAN]
Common Name English
L-LEUCINE, D-PHENYLALANYL-L-PROLYL-L-ARGINYL-L-PROLYLGLYCYLGLYCYLGLYCYLGLYCYL-L-ASPARAGINYLGLYCYL-L-.ALPHA.-ASPARTYL-L-PHENYLALANYL-L-.ALPHA.-GLUTAMYL-L-.ALPHA.-GLUTAMYL-L-ISOLEUCYL-L-PROLYL-L-.ALPHA.-GLUTAMYL-L-.ALPHA.-GLUTAMYL-L-TYROSYL-, 2,2,2-TRIFLUO
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C263
Created by admin on Tue Apr 01 18:11:06 GMT 2025 , Edited by admin on Tue Apr 01 18:11:06 GMT 2025
Code System Code Type Description
USAN
EF-17
Created by admin on Tue Apr 01 18:11:06 GMT 2025 , Edited by admin on Tue Apr 01 18:11:06 GMT 2025
PRIMARY
CAS
1191386-50-1
Created by admin on Tue Apr 01 18:11:06 GMT 2025 , Edited by admin on Tue Apr 01 18:11:06 GMT 2025
PRIMARY
SMS_ID
300000044782
Created by admin on Tue Apr 01 18:11:06 GMT 2025 , Edited by admin on Tue Apr 01 18:11:06 GMT 2025
PRIMARY
FDA UNII
8631NP8608
Created by admin on Tue Apr 01 18:11:06 GMT 2025 , Edited by admin on Tue Apr 01 18:11:06 GMT 2025
PRIMARY
NCI_THESAURUS
C142963
Created by admin on Tue Apr 01 18:11:06 GMT 2025 , Edited by admin on Tue Apr 01 18:11:06 GMT 2025
PRIMARY
RXCUI
2380556
Created by admin on Tue Apr 01 18:11:06 GMT 2025 , Edited by admin on Tue Apr 01 18:11:06 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY

Agent Modifications

Modification Process Modification Role Modification Type Amount Fragment Name Fragment ID
SALT FORMATION Trifluoroacetic acid E5R8Z4G708
Name Property Type Amount Referenced Substance Defining Parameters References
Molecular Formula CHEMICAL
MOL_WEIGHT:NUMBER(CALCULATED) CHEMICAL