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首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Pharmacokinetic and tolerability profile of once-daily zibotentan (ZD4054) in Japanese and Caucasian patients with hormone-resistant prostate cancer.
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Pharmacokinetic and tolerability profile of once-daily zibotentan (ZD4054) in Japanese and Caucasian patients with hormone-resistant prostate cancer.

机译:每日一次zibotentan(ZD4054)在激素抵抗性前列腺癌的日本和白种人患者中的药代动力学和耐受性概况。

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摘要

OBJECTIVE: To investigate potential differences in zibotentan pharmacokinetics between Japanese and Caucasian patients with hormone-resistant prostate cancer (HRPC) following single and multiple dosing. METHODS: In the Japanese study, 18 patients received a single dose of zibotentan 5, 10 or 15 mg followed by 72 h washout before 26 days' once-daily dosing. In the Caucasian study, 21 patients received a single dose of zibotentan 5, 10 or 15 mg followed by 72 h washout before 12 days' once-daily dosing. RESULTS: Pharmacokinetic parameters were similar between populations. Absorption of zibotentan was rapid with maximum plasma concentrations typically achieved within 3 h of dosing. Mean clearance, 17.9 and 18.7 ml/min in Japanese and Caucasian patients, respectively (range 7.0 - 36.3 ml/min in Japanese patients and 7.8 - 29.5 ml/min in Caucasian patients) and volume of distribution, 14.0 and 15.6 l for Japanese and Caucasian patients, respectively (range 7.9 - 29.1 l in Japanese patients and 9.6 - 23.8 l in Caucasian patients) were relatively low, and t1/2 was approximately 12 h (range 5.7 - 18.8 h in Japanese patients and 5.0 - 22.9 h in Caucasian patients) following single dosing. Little accumulation was observed following daily dosing and multiple-dose pharmacokinetics were predictable. Exposure levels achieved in some Japanese patients receiving zibotentan 15 mg were higher than those observed in Caucasian patients, however, this may be due to differences in body weight, as exposure levels were similar when data were normalized for body weight. Zibotentan was well tolerated in both populations. CONCLUSIONS: There are no clinically relevant differences in the disposition and pharmacokinetics of zibotentan between Japanese and Caucasian patients with HRPC.
机译:目的:研究单次和多次给药后,日本人和高加索人荷尔蒙耐药性前列腺癌(HRPC)患者的zibotentan药代动力学的潜在差异。方法:在日本的一项研究中,有18位患者接受了单剂量的zibotentan 5、10或15 mg,随后在每天一次26天的给药前72小时被冲洗。在高加索研究中,有21名患者接受了单剂量的zibotentan 5、10或15 mg,然后在每天一次给药12天之前冲洗72小时。结果:人群之间的药代动力学参数相似。 zibotentan的吸收迅速,通常在给药后3小时内达到最大血浆浓度。平均清除率分别为日本和白种人患者17.9和18.7 ml / min(日本患者为7.0-36.3 ml / min,白种人患者为7.8-29.5 ml / min)和分布体积,日本和白种人分别为14.0和15.6 l高加索患者分别较低(日本患者为7.9-29.1 l,高加索患者为9.6-23.8 l),t1 / 2约为12小时(日本患者为5.7-18.8 h,高加索人为5.0-22.9 h病人)。每日给药后观察到很少的积累,并且可预测多剂量药代动力学。在某些接受zibotentan 15 mg的日本患者中达到的暴露水平高于在白种人患者中观察到的暴露水平,但是,这可能是由于体重的差异,因为将体重数据标准化后的暴露水平相似。 Zibotentan在这两个人群中均耐受良好。结论:日本人和白种人HRPC患者在zibotentan的处置和药代动力学方面无临床相关差异。

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