No pharmacokinetic or pharmacodynamic interaction between atorvastatin and the oral direct thrombin inhibitor ximelagatran

被引:17
作者
Sarich, TC
Schützer, KM
Dorani, H
Wall, U
Kalies, I
Ohlsson, L
Eriksson, UG
机构
[1] AstraZeneca LP, Expt Med, Wilmington, DE 19850 USA
[2] AstraZeneca R&D, Expt Med, Molndal, Sweden
关键词
atorvastatin; ximelagatran; drug interactions; oral direct thrombin inhibitors; thromboembolic disease;
D O I
10.1177/0091270004268047
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:928 / 934
页数:7
相关论文
共 22 条
[21]   Pharmacokinetic-pharmacodynamic drug interactions with HMG-CoA reductase inhibitors [J].
Williams, D ;
Feely, J .
CLINICAL PHARMACOKINETICS, 2002, 41 (05) :343-370
[22]   Consistent pharmacokinetics of the oral direct thrombin inhibitor ximelagatran in patients with nonvalvular atrial fibrillation and in healthy subjects [J].
Wolzt, M ;
Wollbratt, M ;
Svensson, M ;
Wåhlander, K ;
Grind, M ;
Eriksson, UG .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2003, 59 (07) :537-543