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Cerliponase Alfa: First Global Approval

机译:Cerliponase Alfa:第一个全球批准

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摘要

Cerliponase alfa (Brineura (TM)) is a recombinant human tripeptidyl peptidase-1 (TPP1) being developed by BioMarin Pharmaceutical Inc. for use in patients with neuronal ceroid lipofuscinosis type 2 (CLN2), a paediatric neurodegenerative disease caused by a deficiency in TPP1. CLN2 is characterised by progressive impairment of motor function, language deficiencies, seizures, ataxia, blindness and early death, and intracerebroventricular infusion of cerliponase alfa has been shown to reduce the progression of functional decline. This article summarizes the milestones in the development of cerliponase alfa leading to its first global approval in the USA for the treatment of motor function loss in paediatric patients >= 3 years of age with CLN2, and subsequent approval in the EU for CLN2 in all ages.
机译:Cerliponase Alfa(Brineura(TM))是由Biomarin Pharmaceutical Inc.的重组人三肽肽肽酶-1(TPP1),用于患有神经元曲线血管能型2(CLN2)的患者,是由TPP1缺乏引起的儿科神经变性疾病 。 CLN2的特点是运动功能的逐步损害,语言缺陷,癫痫发作,共济失调,失明和早期死亡,并且已显示Cerliponase Alfa的脑室输注,从而降低功能下降的进展。 本文总结了Cerliponase ALFA发展中的里程碑,导致美国的第一个全球批准,用于治疗儿科患者的运动功能损失> = 3岁的CLN2,并随后在所有年龄段的欧盟的欧盟批准 。

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