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达力新药:首次获批

Daridorexant: First Approval.

机构信息

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

出版信息

Drugs. 2022 Apr;82(5):601-607. doi: 10.1007/s40265-022-01699-y.

Abstract

Daridorexant (Quviviq™; Idorsia Pharmaceuticals Ltd.) is an orally administered dual orexin type 1 and type 2 (OX and OX) receptor antagonist (DORA) being developed for the treatment of insomnia. It was selected from a pool of drug candidates on the basis of an expected effect duration of ≈ 8 h at a dose of 25 mg, with a half-life intended to minimize residual effects that might impair daytime functioning. Based on the results of two pivotal phase III trials, daridorexant was recently approved in the USA for the treatment of adult patients with insomnia characterized by difficulties with sleep onset and/or sleep maintenance. This article summarizes the milestones in the development of daridorexant leading to this first approval.

摘要

达力雷沙赞(Quviviq™;Idorsia 制药有限公司)是一种口服双重食欲素 1 型和 2 型(OX 和 OX)受体拮抗剂(DORA),用于治疗失眠症。它是从候选药物库中筛选出来的,预计在 25 毫克剂量下的作用持续时间约为 8 小时,半衰期旨在最大限度地减少可能损害白天功能的残留影响。基于两项关键的 III 期试验结果,达力雷沙赞最近在美国获得批准,用于治疗以入睡和/或维持睡眠困难为特征的成年失眠症患者。本文总结了导致首次批准的达力雷沙赞开发过程中的重要里程碑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b692/9042981/908c5b94e40a/40265_2022_1699_Figa_HTML.jpg

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