Effect of alcohol coadministration on the pharmacodynamics, pharmacokinetics, and safety of lemborexant: A randomized, placebo-controlled crossover study

I. Landry, N. Hall, J. Aluri, G. Filippov, B. Setnik, Satish Dayal, L. Reyderman, M. Moline
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引用次数: 2

Abstract

Background: Lemborexant is a dual orexin receptor antagonist approved to treat insomnia in adults in several countries including the USA, Canada, and Japan. Aims: This study was conducted to investigate effects of lemborexant and alcohol coadministration on postural stability, cognitive performance, and the pharmacokinetics, safety, and tolerability of lemborexant. Methods: This was a Phase 1, double-blind, placebo-controlled, four-period crossover study in 32 healthy adults. Individuals were randomized into one of four treatment sequences to receive single doses of placebo, lemborexant 10 mg (LEM10), alcohol (males, 0.7 g/kg; females, 0.6 g/kg), and LEM10 plus alcohol, each separated by a 14-day washout. Postural stability (body sway) was measured by ataxiameter and a cognitive performance assessment battery evaluated four domains of attention and memory. Results: Pharmacodynamic outcomes were analyzed for the 18 participants who completed all four treatments. Change from baseline in body sway showed no significant differences between lemborexant plus alcohol versus alcohol alone. Compared with alcohol alone, coadministration of lemborexant with alcohol showed additive negative effects on cognitive performance domains, corresponding approximately with peak plasma lemborexant concentrations (median = 1.5 h). Cognitive performance was also impaired with lemborexant alone at 0.5 and 2 h in this experimental paradigm with morning dosing. Alcohol increased plasma lemborexant exposure by 70% based on area under the curve to 72 h, and increased peak plasma lemborexant concentrations by 35%. The most commonly reported treatment–emergent adverse event was somnolence. Conclusion: Coadministration of lemborexant with alcohol showed additive negative effects on cognitive measures, but not on postural stability, compared with alcohol alone. Lemborexant exposure was increased with alcohol. Lemborexant alone or with alcohol was well tolerated. Patients are advised not to consume alcohol with lemborexant.
酒精联合给药对左旋散剂药效学、药代动力学和安全性的影响:一项随机、安慰剂对照的交叉研究
背景:Lemborexant是一种双重食欲素受体拮抗剂,在美国、加拿大和日本等多个国家被批准用于治疗成人失眠。目的:本研究旨在探讨香叶剂和酒精共同给药对姿势稳定性、认知能力以及香叶剂的药代动力学、安全性和耐受性的影响。方法:这是一项一期、双盲、安慰剂对照、四期交叉研究,涉及32名健康成人。个体被随机分为四组治疗序列之一,接受单剂量安慰剂、lemborexant 10 mg (LEM10)、酒精(男性,0.7 g/kg;雌性,0.6 g/kg),和LEM10加酒精,每只分开14天。姿势稳定性(身体摇摆)由ataxiometer测量,认知表现评估电池评估四个领域的注意力和记忆。结果:对完成所有四种治疗的18名参与者的药效学结果进行了分析。从基线开始的身体摇摆变化显示,香氛加酒精与单独使用酒精之间没有显著差异。与单独使用酒精相比,lemborexant与酒精联合使用对认知能力领域产生了附加的负面影响,与血浆中lemborexant浓度峰值(中位数= 1.5 h)大致对应。在这个早晨给药的实验范式中,单独给药0.5和2小时时,认知能力也受到损害。根据曲线下面积计算,酒精使72小时的血浆致病菌暴露增加70%,使血浆致病菌峰值浓度增加35%。最常见的治疗不良事件是嗜睡。结论:与单独使用酒精相比,香叶剂与酒精联合使用对认知功能有负面影响,但对姿势稳定性没有负面影响。随着酒精的增加,Lemborexant暴露增加。Lemborexant单独使用或与酒精一起使用耐受性良好。建议患者在服用香精时不要饮酒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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