Lindegger Nicolas, Sidharta Patricia N, Reseski Kathrin, Dingemanse Jasper
Actelion Pharmaceuticals Ltd, Department of Clinical Pharmacology, Allschwil, Switzerland.
PAREXEL International GmbH, Early Phase Clinical Unit, Klinikum Westend, Haus 31, Spandauer Damm 130, 14050 Berlin, Germany.
Pulm Pharmacol Ther. 2014 Oct;29(1):41-8. doi: 10.1016/j.pupt.2014.04.007. Epub 2014 May 9.
Macitentan is an orally active dual endothelin receptor antagonist, which demonstrated a reduction of the risk of morbidity/mortality events in pulmonary arterial hypertension patients. This double-blind, randomized, placebo- and positive-controlled, four-way crossover thorough QTc study was designed to investigate the effects of therapeutic and supratherapeutic doses of macitentan on cardiac repolarization in healthy male and female subjects. Each subject received the following treatments: moxifloxacin 400 mg, macitentan 10 mg, macitentan 30 mg, and placebo. Each treatment period lasted 9 days and was followed by at least 10 days of washout. The primary endpoint of this study was the baseline-adjusted, placebo-corrected QT interval corrected using the Fridericia method (ΔΔQTcF). Pharmacokinetic (PK), safety, and tolerability assessments were performed during each treatment. A total of 64 subjects were randomized. The upper bound of the 2-sided 90% confidence interval for ΔΔQTcF following macitentan was <10 ms at all time points and no correlation was observed between ΔΔQTcF and PK parameters. Findings in the analysis of the morphological patterns of the ECGs were randomly distributed across all treatments and did not indicate an association with macitentan. Macitentan was well tolerated in this study. Headache and nasopharyngitis were the most frequently reported adverse events. No effects on clinical laboratory and vital signs parameters were observed. In summary, repeated doses of macitentan 10 mg and 30 mg did not indicate any pro-arrhythmic potential.
马昔腾坦是一种口服有效的双重内皮素受体拮抗剂,已证明可降低肺动脉高压患者发病/死亡事件的风险。这项双盲、随机、安慰剂和阳性对照的四交叉全面QTc研究旨在调查治疗剂量和超治疗剂量的马昔腾坦对健康男性和女性受试者心脏复极化的影响。每位受试者接受以下治疗:莫西沙星400毫克、马昔腾坦10毫克、马昔腾坦30毫克和安慰剂。每个治疗期持续9天,随后至少有10天的洗脱期。本研究的主要终点是使用弗里德里西亚方法校正的基线调整、安慰剂校正QT间期(ΔΔQTcF)。在每次治疗期间进行药代动力学(PK)、安全性和耐受性评估。共有64名受试者被随机分组。在所有时间点,马昔腾坦治疗后ΔΔQTcF的双侧90%置信区间上限<10毫秒,且未观察到ΔΔQTcF与PK参数之间存在相关性。心电图形态模式分析结果在所有治疗组中随机分布,未显示与马昔腾坦有关联。在本研究中,马昔腾坦耐受性良好。头痛和鼻咽炎是最常报告的不良事件。未观察到对临床实验室和生命体征参数有影响。总之,重复给予10毫克和30毫克马昔腾坦未显示任何促心律失常潜力。