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替格瑞洛和AR-C124910XX在既往心肌梗死患者中的群体药代动力学

Population pharmacokinetics of ticagrelor and AR-C124910XX in patients with prior myocardial infarction
.

作者信息

Röshammar Daniel, Bergstrand Martin, Andersson Tomas, Storey Robert F, Hamrén Bengt

出版信息

Int J Clin Pharmacol Ther. 2017 May;55(5):416-424. doi: 10.5414/CP202748.

DOI:10.5414/CP202748
PMID:28139972
Abstract

OBJECTIVE

The population pharmacokinetics of ticagrelor and its active metabolite AR-C124910XX were characterized following ticagrelor 60 mg or 90 mg twice daily oral long-term treatment in 4,426 patients with a history of myocardial infarction.

METHODS

The ticagrelor and AR-C124910XX plasma concentration-time data were described by one-compartment models with first-order absorption or metabolite formation and elimination.

RESULTS

Systemic exposure to ticagrelor and AR-C124910XX were stable over time. Ticagrelor apparent clearance (CL/F) was 17 L/h for the 60-mg and 15.4 L/h for the 90-mg dose. The CL/F of AR-C124910XX was 11.1 L/h for the 60-mg and 9.95 L/h for the 90-mg dose. Both ticagrelor and AR-C124910XX CL/F were independently influenced by body weight, sex, age, smoking, and Japanese ethnicity. Female sex and age > 75 years were the only categorical covariates, having more than 20% effect on AR-C124910XX CL/F. Ticagrelor CL/F was 6% higher and 11% lower, whereas AR-C124910XX CL/F was 26% higher and 34% lower for patients weighing 110 and 50 kg, respectively, compared with an 83 kg patient.

CONCLUSIONS: The small differences in exposure to both ticagrelor and AR-C124910XX between demographic subgroups were in accordance with the consistent efficacy and safety outcomes observed across the population. The results were similar to those observed previously in patients with acute coronary syndromes.
.

摘要

目的

在4426例有心肌梗死病史的患者中,对替格瑞洛及其活性代谢产物AR-C124910XX进行每日两次口服60mg或90mg替格瑞洛长期治疗后的群体药代动力学特征研究。

方法

采用具有一级吸收或代谢产物生成及消除的单室模型描述替格瑞洛和AR-C124910XX的血浆浓度-时间数据。

结果

替格瑞洛和AR-C124910XX的全身暴露量随时间稳定。60mg剂量替格瑞洛的表观清除率(CL/F)为17L/h,90mg剂量为15.4L/h。60mg剂量AR-C124910XX的CL/F为11.1L/h,90mg剂量为9.95L/h。替格瑞洛和AR-C124910XX的CL/F均独立受体重、性别、年龄、吸烟和日本种族的影响。女性和年龄>75岁是仅有的分类协变量,对AR-C124910XX的CL/F影响超过20%。与体重83kg的患者相比,体重110kg和50kg的患者替格瑞洛CL/F分别高6%和低11%,而AR-C124910XX的CL/F分别高26%和低34%。

结论

不同人口统计学亚组之间替格瑞洛和AR-C124910XX暴露量的微小差异与在整个人群中观察到的一致疗效和安全性结果相符。结果与先前在急性冠状动脉综合征患者中观察到的相似。

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