Sarich Troy C, Schützer Kajs-Marie, Dorani Hassan, Wall Ulrika, Kalies Inge, Ohlsson Lis, Eriksson Ulf G
Experimental Medicine, AstraZeneca LP, C4C-123, P.O. Box 15437, 1800 Concord Pike, Wilmington, DE 19850, USA.
J Clin Pharmacol. 2004 Aug;44(8):928-34. doi: 10.1177/0091270004268047.
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.
在这项随机、双向交叉研究中,对阿托伐他汀与口服直接凝血酶抑制剂希美加群之间的相互作用可能性进行了研究。健康的男性和女性志愿者(n = 16)接受单次口服40 mg阿托伐他汀,在另一个研究阶段,每天两次服用36 mg希美加群,共5天,并在第4天早晨加服40 mg口服剂量的阿托伐他汀。在完成研究的15名受试者中,对于所有研究参数,包括美拉加群(希美加群的活性形式)的血浆浓度-时间曲线下面积(AUC)和最大血浆浓度、阿托伐他汀酸AUC以及活性3-羟基-3-甲基戊二酰辅酶A(HMG-CoA)还原酶抑制剂的AUC,均未检测到阿托伐他汀与希美加群之间存在药代动力学相互作用。阿托伐他汀并未改变美拉加群诱导的活化部分凝血活酶时间延长,两种药物联合使用时耐受性良好。总之,在本研究中未观察到阿托伐他汀与希美加群之间存在药代动力学或药效学相互作用。