IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Karin de Haart, Keiko Asao, Quazi Ataher, Jamie Geier, Jodie Hillen, Kui Huang, Peter G M Mol, Donna Rivera, Huifen Wang, Hong Yang, Siyan Zhan, Wilhelmina E Hoogendoorn, Lourens T Bloem
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引用次数: 0

摘要

基因疗法是可以彻底改变医疗保健的创新疗法。鉴于其独特的作用机制、制造和给药方法以及产生长期影响的潜力,基因疗法在获得授权后需要对其安全性和有效性进行长期跟踪(LTFU),通常需要使用真实世界数据(RWD)。目前有 2000 多种基因疗法正在开发中,因此需要对 LTFU 研究进行知识积累。在此,我们从全球角度回顾了使用真实世界数据进行 LTFU 研究的监管、科学和操作要求及注意事项。本综述中的见解可为基因疗法的授权后 LTFU 研究提供支持,从而有助于安全有效地使用基因疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term follow-up after authorization of gene therapy: leveraging real-world data.

Gene therapies are innovative treatments that could revolutionize healthcare. Given their unique mechanisms of action, methods of manufacturing and administration, and the potential for long-lasting impact, gene therapies require long-term follow-up (LTFU) of safety and effectiveness post authorization, often using real-world data (RWD). With over 2000 gene therapies in development, there is a need for knowledge-building regarding LTFU studies. Here, we review regulatory, scientific, and operational requirements and considerations for LTFU studies using RWD from a global perspective. The insights in this review support post-authorization LTFU studies for gene therapies, thereby contributing to their safe and effective use.

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来源期刊
Drug Discovery Today
Drug Discovery Today 医学-药学
CiteScore
14.80
自引率
2.70%
发文量
293
审稿时长
6 months
期刊介绍: Drug Discovery Today delivers informed and highly current reviews for the discovery community. The magazine addresses not only the rapid scientific developments in drug discovery associated technologies but also the management, commercial and regulatory issues that increasingly play a part in how R&D is planned, structured and executed. Features include comment by international experts, news and analysis of important developments, reviews of key scientific and strategic issues, overviews of recent progress in specific therapeutic areas and conference reports.
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