Mueller Markus S, Shakeri-Nejad Kasra, Gutierrez Marcelo M, Krause Andreas, Täubel Jörg, Sanderson Brian, Dingemanse Jasper
*Department of Clinical Pharmacology, Actelion Pharmaceuticals Ltd, Allschwil, Switzerland; †Richmond Pharmacology Ltd, St George's University of London, London, United Kingdom; and ‡Chiltern (Early Phase) Ltd, Dundee, United Kingdom.
J Cardiovasc Pharmacol. 2014 Feb;63(2):120-31. doi: 10.1097/FJC.0000000000000030.
ACT-280778 is a novel nondihydropyridine dual L/T-type calcium channel blocker. Two clinical studies (AC-067-101 and AC-067-102) were conducted to characterize its safety, tolerability, and pharmacokinetics in healthy male subjects after oral administration of single and multiple doses. Both trials were single-center, randomized, double-blind, placebo-controlled, adaptive design, ascending-dose studies, in which ACT-280778 was administrated as single doses of 2, 5, 15, or 40 mg, or as once-daily doses of 5 or 15 mg for 7 days. Single and multiple doses up to and including 15 mg were well tolerated, and no serious or severe adverse event was reported in either study. A single dose of 40 mg was associated with abnormal electrocardiogram findings resulting in the discontinuation of further treatment at this dose or higher doses. ACT-280778 was rapidly absorbed, and larger than dose-proportional increases of the maximum plasma concentration and area under the plasma concentration-time curve were observed. Food intake delayed the time to maximum plasma concentration and doubled exposure. Urinary excretion of unchanged ACT-280778 was negligible, and accumulation at steady state was modest. Overall, pharmacokinetic and tolerability profiles of ACT-280778 observed in these 2 studies warranted further evaluation of ACT-280778 in a proof-of-concept study in patients with hypertension.
ACT-280778是一种新型非二氢吡啶类L/T型双钙通道阻滞剂。开展了两项临床研究(AC-067-101和AC-067-102),以表征其在健康男性受试者口服单剂量和多剂量后的安全性、耐受性和药代动力学。两项试验均为单中心、随机、双盲、安慰剂对照、适应性设计、递增剂量研究,其中ACT-280778的给药剂量为单剂量2、5、15或40mg,或每日一次剂量5或15mg,共7天。高达并包括15mg的单剂量和多剂量耐受性良好,两项研究均未报告严重或重度不良事件。单剂量40mg与心电图异常结果相关,导致该剂量及更高剂量的进一步治疗中断。ACT-280778吸收迅速,观察到最大血浆浓度和血浆浓度-时间曲线下面积呈大于剂量比例的增加。食物摄入延迟了达到最大血浆浓度的时间,并使暴露量加倍。未改变的ACT-280778的尿排泄可忽略不计,稳态时的蓄积适度。总体而言,在这两项研究中观察到的ACT-280778的药代动力学和耐受性概况值得在高血压患者的概念验证研究中对ACT-280778进行进一步评估。