Department of Clinical Pharmacology, Actelion Pharmaceuticals Ltd, Allschwil, Switzerland.
Pharmacology. 2013;91(5-6):331-8. doi: 10.1159/000351704. Epub 2013 Jun 26.
BACKGROUND/AIMS: Macitentan is a novel dual endothelin receptor antagonist with sustained receptor binding in clinical development for pulmonary arterial hypertension. The present study compared the pharmacokinetics and safety of macitentan in healthy Caucasian and Japanese subjects and explored the potential sex differences.
In this single-center, open-label, phase I study 10 healthy subjects of each ethnic origin with a male/female ratio of 1:1 in each group were administered a single oral 10-mg dose of macitentan. Blood samples were taken to determine plasma levels of macitentan and its pharmacologically active metabolite, ACT-132577, and safety and tolerability were monitored using standard assessments.
For both macitentan and its metabolite, values for Cmax were similar but a shorter half-life was determined in Japanese subjects resulting in an exposure to both compounds being approximately 15% lower in Japanese when compared to Caucasian subjects. The exposure to macitentan was similar in Japanese males and females whereas Caucasian females had an approximately 25% higher exposure than Caucasian males. In both ethnic groups, females had an approximately 15% higher exposure to ACT-132577 than male subjects. Macitentan was well tolerated in both ethnic groups. There were no clinically significant differences in adverse event profile, clinical laboratory, electrocardiographic parameters, and vital signs between both groups.
The data suggest that the minor differences in pharmacokinetics between the two groups are not clinically relevant and no dose adjustment of macitentan based on Japanese ethnic origin or sex is necessary.
背景/目的:马西替坦是一种新型的双重内皮素受体拮抗剂,在肺动脉高压的临床开发中具有持续的受体结合。本研究比较了马西替坦在健康白种人和日本受试者中的药代动力学和安全性,并探讨了潜在的性别差异。
在这项单中心、开放标签、I 期研究中,每组各有 10 名白种人和 10 名日本健康受试者,男女比例为 1:1,均单次口服 10mg 马西替坦。采集血样以确定马西替坦及其具有药理活性的代谢物 ACT-132577 的血浆水平,并使用标准评估监测安全性和耐受性。
对于马西替坦及其代谢物,Cmax 值相似,但日本受试者的半衰期较短,导致与白种人相比,日本受试者的两种化合物暴露量约低 15%。马西替坦在日本男性和女性中的暴露量相似,而白种女性的暴露量比白种男性高约 25%。在两个种族群体中,女性对 ACT-132577 的暴露量比男性高约 15%。马西替坦在两个种族群体中均耐受良好。两组之间的不良事件谱、临床实验室、心电图参数和生命体征没有临床意义上的差异。
数据表明,两组之间药代动力学的微小差异无临床意义,无需根据日本种族或性别调整马西替坦的剂量。