abeparvovec促性腺激素原治疗脊髓性肌萎缩(SMN1)的评价

IF 0.8 4区 医学 Q4 PHARMACOLOGY & PHARMACY Expert Opinion on Orphan Drugs Pub Date : 2021-10-03 DOI:10.1080/21678707.2021.2003778
M. Waldrop, A. Connolly, J. Mendell
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引用次数: 0

摘要

摘要简介Onasemnogene abeparvovec是美国食品药品监督管理局批准的第一种针对任何遗传性疾病的系统性基因替代疗法,也是美国食品药品监管局批准的第二种针对5q脊髓性肌萎缩症的基因疗法。涵盖的领域我们讨论了阿贝伐韦onasemnogene的设计和临床前开发,以及专注于疗效和安全性的临床试验和真实世界数据。专家意见尽管onasemnogene abeparvovec对治疗5q SMA非常有效,但它只被批准在2岁以下使用,还有另外两种FDA批准的基于分子的治疗方法。在治疗选择、剂量优化的可能性和联合治疗方面仍然存在许多问题。
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An evaluation of onasemnogene abeparvovec for spinal muscular atrophy (SMN1)
ABSTRACT Introduction Onasemnogene abeparvovec is the first systemic gene replacement therapy approved by the FDA for any inherited condition and is the second FDA-approved genetic therapy for 5q spinal muscular atrophy. Areas covered We discuss the design and preclinical development of onasemnogene abeparvovec, along with clinical trial and real-world data focusing on efficacy and safety. Expert Opinion Although onasemnogene abeparvovec is strikingly effective for the treatment of 5q SMA, it is only approved for use under the age of 2 years and there are also two other FDA-approved molecular-based treatments. Many questions remain in terms of treatment selection, possibility of dose optimization, and combinational therapies.
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来源期刊
Expert Opinion on Orphan Drugs
Expert Opinion on Orphan Drugs PHARMACOLOGY & PHARMACY-
CiteScore
2.30
自引率
0.00%
发文量
8
期刊介绍: Expert Opinion on Orphan Drugs is an international, peer-reviewed journal that covers all aspects of R&D on rare diseases and orphan drugs.
期刊最新文献
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