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治疗失眠的雷美替胺治疗后缺乏残余晨效:9 项临床试验结果总结。

Lack of residual morning effects of lemborexant treatment for insomnia: summary of findings across 9 clinical trials.

机构信息

Neurobiology Business Group, Eisai Inc ., Woodcliff Lake, New Jersey, USA.

Clinilabs Drug Development Corporation , New York, New York, USA.

出版信息

Postgrad Med. 2021 Jan;133(1):71-81. doi: 10.1080/00325481.2020.1823724. Epub 2020 Oct 29.

Abstract

OBJECTIVES

Residual next-day effects of sleep-promoting drugs are common and an important safety issue. Lemborexant is a dual orexin receptor antagonist approved in the United States and Japan for treatment of insomnia in adults. We evaluated the potential of lemborexant for residual morning and next-day effects, including somnolence, based on lemborexant clinical study findings.

METHODS

This paper reports findings from 9 lemborexant clinical studies that incorporated next-day assessments of residual drug effects, based on published findings and data on file. Results are reported for healthy subjects or subjects with insomnia disorder treated with lemborexant 5 mg/day or 10 mg/day, placebo, or active comparator before bedtime. Outcomes assessed included next-morning postural stability (body sway measured by ataxiameter), cognitive performance (Cognitive Performance Assessment Battery), impact on driving (standard deviation of lateral position during highway driving test), subjective sleepiness (sleep diary entries), and adverse events of somnolence.

RESULTS

Change from baseline in postural stability the morning after lemborexant administration did not differ from placebo. Among 4 Cognitive Performance Assessment Battery measures, only power of attention declined significantly more with lemborexant treatment compared with placebo in 1 of 2 studies, whereas zolpidem differed from placebo on multiple measures. On the highway-driving test, lemborexant did not significantly impair driving performance versus placebo, however, zopiclone did differ. In large phase 3 trials, next-morning sleep diary ratings showed significantly greater alertness with lemborexant compared with placebo after up to 6 months of treatment. As expected, somnolence was the most common adverse event reported with lemborexant treatment. Somnolence was typically mild to moderate in severity and rarely caused discontinuation of study drug.

CONCLUSION

Across 9 clinical studies, lemborexant did not substantially impair next-day functioning among healthy subjects and subjects with insomnia.

摘要

目的

助眠药物的残留次日效应很常见,是一个重要的安全问题。雷美替胺是一种双重食欲素受体拮抗剂,已获美国和日本批准用于治疗成人失眠。我们根据雷美替胺的临床研究结果,评估了雷美替胺残留晨后和次日效应(包括嗜睡)的潜在风险。

方法

本文报告了 9 项雷美替胺临床研究的结果,这些研究纳入了次日评估残留药物效应的内容,依据的是已发表的研究结果和存档数据。结果报告了健康受试者或失眠症受试者在睡前接受雷美替胺 5mg/天或 10mg/天、安慰剂或阳性对照药物治疗后的情况。评估的结局包括次日姿势稳定性(用摆锤仪测量的身体摆动)、认知表现(认知表现评估成套测验)、对驾驶的影响(高速公路驾驶测试中的侧向位置标准差)、主观嗜睡(睡眠日记条目)和嗜睡相关不良事件。

结果

与安慰剂相比,雷美替胺给药后次日清晨姿势稳定性的基线变化无差异。在 4 项认知表现评估成套测验的测量指标中,只有注意力效能在 2 项研究中的 1 项中较安慰剂显著下降,而唑吡坦在多项指标中与安慰剂不同。在高速公路驾驶测试中,雷美替胺与安慰剂相比并未显著损害驾驶表现,但佐匹克隆则不同。在大型 3 期试验中,经过长达 6 个月的治疗,与安慰剂相比,雷美替胺在次日早晨的睡眠日记评分中显示出了更显著的警觉性。不出所料,与雷美替胺治疗相关的最常见不良事件是嗜睡。嗜睡通常为轻至中度,很少导致研究药物停药。

结论

在 9 项临床研究中,雷美替胺在健康受试者和失眠症受试者中并未明显损害次日的功能。

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