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Dabigatran: An Oral Novel Potent Reversible Nonpeptide Inhibitor of Thrombin
Author(s) -
Wolfgang G. Eisert,
Norbert Hauel,
Joachim Stangier,
Wolfgang Wienen,
Andreas Clemens,
Joanne van Ryn
Publication year - 2010
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.110.203604
Subject(s) - dabigatran , medicine , prodrug , direct thrombin inhibitor , pharmacology , discovery and development of direct thrombin inhibitors , antithrombotic , pharmacodynamics , antithrombins , warfarin , thrombin , drug , anesthesia , pharmacokinetics , atrial fibrillation , platelet
Dabigatran is a highly selective, reversible, and potent thrombin inhibitor and is orally available as the prodrug, dabigatran etexilate. It has shown antithrombotic efficacy in animal models of thrombosis, with a rapid onset of action and predictable pharmacodynamic response. Peak plasma concentrations of dabigatran occur 1 to 2 hours after ingestion of the prodrug. The terminal half-life of dabigatran is 12 to 14 hours in elderly volunteers. Dabigatran is not metabolized by cytochrome P450 isoenzymes and does not interact with food. Dabigatran has a low potential for drug-drug interactions and is predominantly renally excreted. Dabigatran etexilate as chronic therapy effectively prevents the recurrence of venous thromboembolism and cardioembolic stroke. For the first time, it has been demonstrated clinically that there may be an effective and safe alternative to warfarin.

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