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雷美替胺:首次批准

Lemborexant: First Approval.

机构信息

Springer Nature, Mairangi Bay, Private Bag 65901, Auckland, 0754, New Zealand.

出版信息

Drugs. 2020 Mar;80(4):425-432. doi: 10.1007/s40265-020-01276-1.

Abstract

Lemborexant (DAYVIGO™) is an orally administered, dual orexin receptor (OXR) antagonist that exhibits reversible competitive antagonism at OXR1 and OXR2 (> affinity at OXR2) that was discovered and developed by Eisai Inc. for the treatment of adult patients with insomnia. In December 2019, lemborexant received its first approval (with final interim scheduling) in the USA for the treatment of adult patients with insomnia, characterized by difficulties with sleep onset and/or sleep maintenance. In January 2020, lemborexant also received approval in Japan for the treatment of insomnia. It is also being investigated for the treatment of irregular sleep-wake rhythm disorder (ISWRD) associated with mild to moderate Alzheimer's disease. This article summarizes the milestones in the development of lemborexant leading to its first global approval.

摘要

雷美替胺(DAYVIGO™)是一种口服的双食欲素受体(OXR)拮抗剂,对 OXR1 和 OXR2 具有可逆竞争性拮抗作用(对 OXR2 的亲和力>),由卫材株式会社发现并开发,用于治疗成人失眠症。2019 年 12 月,雷美替胺在美国首次获批(最终临时安排),用于治疗以入睡和/或维持睡眠困难为特征的成人失眠症。2020 年 1 月,雷美替胺在日本也获得批准用于治疗失眠症。它也正在被研究用于治疗与轻度至中度阿尔茨海默病相关的不规则睡眠-觉醒节律障碍(ISWRD)。本文总结了雷美替胺开发过程中的重要里程碑,直至其在全球范围内首次获得批准。

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