依维莫司:首次批准。

Evinacumab: First Approval.

机构信息

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

出版信息

Drugs. 2021 Jun;81(9):1101-1105. doi: 10.1007/s40265-021-01516-y. Epub 2021 May 18.

Abstract

The recombinant human monoclonal antibody evinacumab (evinacumab-dgnb, EVKEEZA™) is an angiopoietin-like protein three (ANGPTL3) inhibitor that has been developed by Regeneron Pharmaceuticals for the treatment of homozygous familial hypercholesterolaemia (HoFH), refractory hypercholesterolemia (both familial and non-familial) and severe hypertriglyceridaemia. Based on the results of the phase III ELIPSE HoFH trial, evinacumab was recently approved in the USA as an adjunct to other LDL-C lowering therapies for the treatment of adult and paediatric patients aged 12 years and older with HoFH, and has received a positive opinion in the EU. This article summarizes the milestones in the development of evinacumab leading to this first approval for HoFH.

摘要

人源化单克隆抗体依维莫司(依维莫司-dgnb,EVKEEZA™)是一种血管生成素样蛋白 3(ANGPTL3)抑制剂,由再生元制药公司开发,用于治疗纯合子家族性高胆固醇血症(HoFH)、难治性高胆固醇血症(家族性和非家族性)和严重高甘油三酯血症。基于 III 期 ELIPSE HoFH 试验的结果,依维莫司最近在美国获得批准,与其他 LDL-C 降低疗法联合用于治疗 12 岁及以上 HoFH 成人和儿科患者,并在欧盟获得积极意见。本文总结了依维莫司开发过程中的重要里程碑,最终使其获得 HoFH 的首次批准。

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