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替格瑞洛与阿托伐他汀或辛伐他汀在健康志愿者中合用的药代动力学相互作用研究。

Pharmacokinetic interaction studies of co-administration of ticagrelor and atorvastatin or simvastatin in healthy volunteers.

机构信息

Clinical Pharmacology, AstraZeneca LP, OW3-117, 1800 Concord Pike, PO Box 15437, Wilmington, DE 19850-5437, USA.

出版信息

Eur J Clin Pharmacol. 2013 Mar;69(3):477-87. doi: 10.1007/s00228-012-1369-4. Epub 2012 Aug 25.

DOI:10.1007/s00228-012-1369-4
PMID:22922682
Abstract

PURPOSE

Interactions between ticagrelor and atorvastatin or simvastatin were investigated in two-way crossover studies.

METHODS

Both studies were open-label for statin; the atorvastatin study was placebo-controlled for ticagrelor. For atorvastatin, volunteers (n = 24) received ticagrelor (loading dose 270 mg; 90 mg twice daily, 7 days) or placebo, plus atorvastatin calcium (80 mg; day 5). For simvastatin, volunteers (n = 24) received simvastatin 80 mg, or ticagrelor (loading dose 270 mg; 180 mg twice daily, 7 days) plus simvastatin (80 mg; day 5). In each study, volunteers received the alternate treatment after washout (≥ 7 days).

RESULTS

Ticagrelor increased mean atorvastatin maximum plasma concentration (C(max)) and area under the plasma concentration-time curve from zero to infinity (AUC) by 23 % and 36 %, respectively. Simvastatin C(max) and AUC were increased by 81 % and 56 % with ticagrelor. Ticagrelor also increased C(max) and AUC of analysed atorvastatin metabolites by 13-55 % and 32-67 %, respectively, and simvastatin acid by 64 % and 52 %, respectively. Co-administration of ticagrelor with each statin was well tolerated.

CONCLUSIONS

Exposure to ticagrelor and its active metabolite, AR-C124910XX, was generally unchanged by a single dose of either statin, except for a minor increase in ticagrelor C(max) in the presence of simvastatin. Effects of ticagrelor on atorvastatin pharmacokinetics were modest and unlikely clinically relevant, while with simvastatin, changes were slightly larger, and simvastatin doses >40 mg with ticagrelor should be avoided.

摘要

目的

在两项交叉研究中研究替格瑞洛与阿托伐他汀或辛伐他汀的相互作用。

方法

两项研究均对他汀类药物进行开放性研究;阿托伐他汀研究替格瑞洛为安慰剂对照。对于阿托伐他汀,志愿者(n=24)接受替格瑞洛(负荷剂量 270 mg;90 mg 每日 2 次,7 天)或安慰剂,加阿托伐他汀钙(80 mg;第 5 天)。对于辛伐他汀,志愿者(n=24)接受辛伐他汀 80 mg,或替格瑞洛(负荷剂量 270 mg;180 mg 每日 2 次,7 天)加辛伐他汀(80 mg;第 5 天)。在每项研究中,志愿者在洗脱(≥7 天)后接受交替治疗。

结果

替格瑞洛使阿托伐他汀最大血浆浓度(C(max))和从 0 到无穷大的血浆浓度-时间曲线下面积(AUC)分别增加 23%和 36%。替格瑞洛使辛伐他汀 C(max)和 AUC 分别增加 81%和 56%。替格瑞洛还使阿托伐他汀代谢物的 C(max)和 AUC 分别增加 13-55%和 32-67%,而使辛伐他汀酸的 C(max)和 AUC 分别增加 64%和 52%。替格瑞洛与每种他汀类药物联合使用均耐受良好。

结论

除了替格瑞洛与辛伐他汀合用会使替格瑞洛 C(max)略有增加外,阿托伐他汀和其活性代谢物 AR-C124910XX 的单次剂量暴露通常不受其他他汀类药物的影响。替格瑞洛对阿托伐他汀药代动力学的影响是适度的,不太可能具有临床相关性,而与辛伐他汀合用,变化略大,替格瑞洛与辛伐他汀合用剂量应避免大于 40mg。

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