Semin Vasc Med 2005; 5(3): 245-253
DOI: 10.1055/s-2005-916163
Copyright © 2005 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA.

Pharmacokinetics and Pharmacodynamics of Ximelagatran

Michael Wolzt1 , Troy S. Sarich2 , Ulf G. Eriksson3
  • 1Clinical Pharmacology, Allgemeines Krankenhaus Wien, Waehringer Guertel 18-20, Medical University of Vienna, Vienna, Austria
  • 2AstraZeneca LP, Wilmington, Delaware
  • 3AstraZeneca R&D, Mölndal, Sweden
Further Information

Publication History

Publication Date:
25 August 2005 (online)

ABSTRACT

Oral anticoagulant therapy with vitamin K antagonists (VKAs) such as warfarin has proven benefits in the treatment and prevention of thromboembolic disorders but has important limitations that result in substantial underuse. In particular, the VKAs have variable and unpredictable pharmacokinetics and pharmacodynamics and a narrow separation between antithrombotic and hemorrhagic effects that necessitates careful dose adjustment based on frequent coagulation monitoring. In contrast, the oral direct thrombin inhibitor ximelagatran has a predictable and reproducible pharmacokinetic/pharmacodynamic profile that allows treatment using fixed-dose regimens without coagulation monitoring. The bioavailability of melagatran, the active form of ximelagatran, after oral administration of ximelagatran is ∼20% with low inter- and intra-individual variability. Peak plasma melagatran concentrations are reached ∼2 hours after oral dosing of ximelagatran to healthy volunteers, and melagatran is eliminated with a half-life of ∼3 hours with clearance predominantly by renal excretion. Hence, a higher melagatran exposure is seen in patients with renal failure; ximelagatran is currently not recommended for patients with severe renal impairment (creatinine clearance of <30 mL/min) as these patients were not included in the clinical trial program. Exposure to melagatran increases linearly with the ximelagatran dose. The pharmacokinetic/pharmacodynamic profile is consistent across a broad range of different patient populations and is unaffected by gender, age, body weight, ethnic origin, obesity, and mild-to-moderate hepatic impairment. Any differences in melagatran pharmacokinetics associated with these factors are attributable to differences in renal function.

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Michael WolztM.D. 

Clinical Pharmacology, Allgemeines Krankenhaus Wien

Medical University of Vienna, Austria A-1090