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帕罗维罗替治疗法:首次批准。

Palovarotene: First Approval.

机构信息

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

出版信息

Drugs. 2022 Apr;82(6):711-716. doi: 10.1007/s40265-022-01709-z.

Abstract

Palovarotene (Sohonos™) is an orally bioavailable selective retinoic acid receptor (RAR)γ agonist being developed by Ipsen for the reduction of heterotopic ossification (HO) formation in patients with fibrodysplasia ossificans progressiva (FOP). By binding to RARγ, palovarotene inhibits bone morphogenetic protein and SMAD 1/5/8 signalling: interfering with these pathways prevents chondrogenesis and ultimately HO by permitting normal muscle tissue repair or regeneration to occur. Palovarotene received its first approval on 21 January 2022 to reduce the formation of HO in adults and children aged 8 years and above for females and 10 years and above for males with FOP in Canada. This article summarizes the milestones in the development of palovarotene leading to this first approval.

摘要

帕罗伐罗替酯(Sohonos™)是 Ipsen 公司研发的一种口服生物利用的选择性维甲酸受体(RAR)γ激动剂,用于减少进行性骨化性纤维发育不良(FOP)患者的异位骨化(HO)形成。帕罗伐罗替酯通过与 RARγ 结合,抑制骨形态发生蛋白和 SMAD1/5/8 信号转导:干扰这些途径可通过允许正常肌肉组织修复或再生来防止软骨生成和最终的 HO 发生。帕罗伐罗替酯于 2022 年 1 月 21 日首次在加拿大获得批准,用于减少 FOP 女性 8 岁及以上和男性 10 岁及以上患者的 HO 形成。本文总结了导致这一首次批准的帕罗伐罗替酯研发的里程碑事件。

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