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首页> 外文期刊>Cardiovascular therapeutics >Age and sex effects on the single- and multiple-dose safety and pharmacokinetics of the new renin inhibitor ACT-178882
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Age and sex effects on the single- and multiple-dose safety and pharmacokinetics of the new renin inhibitor ACT-178882

机译:年龄和性别对新型肾素抑制剂ACT-178882的单剂量和多剂量安全性及药代动力学的影响

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Aim: To investigate the effect of age and sex on the single- and multiple-dose safety and pharmacokinetics of ACT-178882, a new direct renin inhibitor. Methods: In the single-dose, open-label part of the study, healthy young and elderly male and female subjects received a dose of 300 mg ACT-178882. In the multiple-dose, double-blind, placebo-controlled part of the study, healthy elderly male and female subjects received ACT-178882 (300 or 600 mg) or placebo once-a-day for 14 days. Results: Mild headache and diarrhea were the most common adverse events in the single- and multiple-dose parts, respectively. The frequency of diarrhea increased dose dependently, and no placebo subjects reported this adverse event. Administration of ACT-178882 did not result in any clinically relevant changes in ECG, vial signs, clinical laboratory, body weight, or physical examination. In the single-dose part and independent of sex, values for Cmax and AUC0-∞ were about 85% higher in elderly compared with young subjects, and t1/2 was about 5 h longer (29.3 vs. 24.1 h). In both age groups, plasma ACT-178882 concentrations were slightly higher in female versus male subjects. Following multiple-dose administration to elderly subjects, accumulation of ACT-178882 was moderate, about 1.8-fold, t1/2 was unchanged as compared with single-dose administration, sex effects were minimal, and the increase in the exposure with increasing dose appeared less than dose proportional. Conclusion: Overall, single- and multiple-dose administration of ACT-178882 was well tolerated. No dose adaptation based on sex is necessary, whereas a dose reduction based on age could be considered.
机译:目的:研究年龄和性别对新型直接肾素抑制剂ACT-178882的单剂量和多剂量安全性及药代动力学的影响。方法:在这项单剂量,开放标签的研究中,健康的男女老少受试者接受300 mg ACT-178882的剂量。在多剂量,双盲,安慰剂对照的研究中,健康的老年男性和女性受试者每天一次接受ACT-178882(300或600 mg)或安慰剂,共14天。结果:轻度头痛和腹泻分别是单剂量和多剂量部位最常见的不良事件。腹泻的频率依赖于剂量增加,并且没有安慰剂受试者报告这种不良事件。 ACT-178882的使用并未导致ECG,小瓶体征,临床实验室检查,体重或体检的任何临床相关变化。在单剂量部分,与性别无关,老年人的Cmax和AUC0-∞值比年轻受试者高约85%,t1 / 2约长5 h(29.3 vs. 24.1 h)。在两个年龄组中,女性受试者的血浆ACT-178882浓度均略高于男性受试者。在对老年受试者进行多剂量给药后,与单剂量给药相比,ACT-178882的蓄积中等,约为1.8倍,t1 / 2不变,性别影响很小,并且随着剂量的增加暴露量增加小于剂量比例。结论:ACT-178882的整体,单剂量和多剂量给药耐受性良好。无需根据性别调整剂量,而可以考虑根据年龄降低剂量。

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