The Journal of Clinical Pharmacology · 2004 · 23 citations · 17 references
MedicinePharmacokineticsPharmacologyCardiovascular PharmacotherapyClinical PharmacologyPharmacodynamicsAnticoagulant TherapyPharmacokinetic Drug InteractionsActivated Partial Thromboplastin Time ProlongationArea Under The Plasma Concentration-time CurveDirect Thrombin InhibitorsHmg-coa Reductase InhibitorsIsolated Prolonged Activated Partial Thromboplastin TimePharmacokinetic Interaction MechanismsPlasma Concentration - Time ProfilePlasma Concentration-time Analysis
In this randomized, 2-way crossover study, the potential for interaction was investigated between atorvastatin and ximelagatran, an oral direct thrombin inhibitor. Healthy female and male volunteers (n = 16) received atorvastatin 40 mg as a single oral dose and, in a separate study period, ximelagatran 36 mg twice daily for 5 days plus a 40-mg oral dose of atorvastatin on the morning of day 4. In the 15 subjects completing the study, no pharmacokinetic interaction was detected between atorvastatin and ximelagatran for all parameters investigated, including melagatran (the active form of ximelagatran) area under the plasma concentration versus time curve (AUC) and maximum plasma concentration, atorvastatin acid AUC, and AUC of active 3-hydroxy-3-methyl-glutaryl-coenzyme-A (HMG-CoA) reductase inhibitors. Atorvastatin did not alter the melagatran-induced prolongation of the activated partial thromboplastin time, and both drugs were well tolerated when administered in combination. In conclusion, no pharmacokinetic or pharmacodynamic interaction between atorvastatin and ximelagatran was observed in this study.
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Alfred W. Alberts, J Chen, G. W. Kuron et al. · Proceedings of the National Academy of Sciences · 1980 · 1.6K citations · Full text
Giancarlo Agnelli, Alexander T. Cohen, Ola E. Dahl et al. · Thrombosis and Haemostasis · 2003 · 252 citations