罕见病研究2024,Vol.3Issue(3) :345-349.DOI:10.12376/j.issn.2097-0501.2024.03.011

《罕见病基因治疗产品临床试验技术指导原则(试行)》解读

The Interpretation of Guideline for Clinical Trials Design of Gene Therapy Products for Rare Diseases(Trial Version)

刘晓 伍熙源 鲁爽
罕见病研究2024,Vol.3Issue(3) :345-349.DOI:10.12376/j.issn.2097-0501.2024.03.011

《罕见病基因治疗产品临床试验技术指导原则(试行)》解读

The Interpretation of Guideline for Clinical Trials Design of Gene Therapy Products for Rare Diseases(Trial Version)

刘晓 1伍熙源 1鲁爽1
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作者信息

  • 1. 国家药品监督管理局药品审评中心,北京 100076
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摘要

近年来,在国家政策激励和监管改革的持续推动下,中国罕见病药物研发持续增长未来可期.截至2024年3月,国内已有30余款用于罕见病的基因治疗产品获得临床试验默示许可.为指导和规范罕见病基因治疗产品的临床试验设计,国家药品监督管理局药品审评中心发布了《罕见病基因治疗产品临床试验技术指导原则(试行)》,现予以解读,为业界提供参考.

Abstract

In recent years,driven by policy incentives and regulatory reforms,the research and devel-opment of rare disease drugs in China has begun to show a promising future.As of March 2024,more than 30 gene therapy products for rare diseases in China have been approved for clinical trials.In order to guide the clinical trial design of gene therapy products for rare diseases,Center for Drug Evaluation,National Medical Products Administration has issued Guideline for Clinical Trials Design of Gene Therapy Products for Rare Disea-ses(Trial Version).Now we try to interpret this guideline to provide recommendations for the industry.

关键词

罕见病/基因治疗/临床试验/审评考虑

Key words

rare diseases/gene therapy/clinical trials/review considerations

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出版年

2024
罕见病研究

罕见病研究

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