中国药物警戒 ›› 2021, Vol. 18 ›› Issue (1): 47-51.
DOI: 10.19803/j.1672-8629.2021.01.09

• 法规与管理研究 • 上一篇    下一篇

拓展性同情使用临床试验用药制度的相关问题研究

马静, 高京宏, 刘春光*   

  1. 武警北京总队医院药剂科,北京 100027
  • 收稿日期:2020-04-22 修回日期:2021-01-18 出版日期:2021-01-15 发布日期:2021-01-18
  • 通讯作者: *刘春光,女,硕士,主管药师,药物警戒与合理用药。E-mail:liuchunguang2019@163.com
  • 作者简介:马静,女,博士,主任医师,临床医学与卫勤学。

Issues Related to Expanded Access to Investigational Drugs for Compassionate Use

MA Jing, GAO Jinghong, LIU Chunguang*   

  1. Department of Pharmacy,Beijing Corps Hospital of Chinese People's Armed Police Force,Beijing 100027,China
  • Received:2020-04-22 Revised:2021-01-18 Online:2021-01-15 Published:2021-01-18

摘要: 目的 研究国外部分国家拓展性同情使用临床试验用药制度及申请批准情况,为我国拓展性临床试验用药制度设计提供参考。方法 通过查阅美国、欧盟药品监管机构发布的法规政策、技术指南、年度报告及相关文献,深入分析欧美拓展性临床试验用药的相关概念、类别、申请要求、风险获益评估等内容。结果 和结论 拓展性同情使用临床试验用药是在不能通过已上市药物有效治疗严重疾病或危及生命疾病时,获得研究药物的潜在方式。美欧等地区对拓展性研究药物制定了较为完善的法规体系,因为临床试验用药并未上市,安全性和有效性证据收集不足,使用时更要保护使用者的安全,同时伦理委员会应当严格履行职责,保证患者知情同意,并对治疗方案严格审查。

关键词: 拓展性, 同情使用, 临床试验用药

Abstract: Objective To study the laws and regulations and application approval by some foreign drug regulatory agencies concerning expanded access to investigational drugs for treatment use so as to provide reference for the design of related guidelines in China.Methods By referring to the laws and regulations,technical guidelines,annual reports and relevant literature issued by drug regulatory agencies of the United States and the European Union,the relevant concepts,categories,application requirements,risk and benefit assessment of drugs used in overseas extended clinical trials were analyzed in depth.Results and Conclusion Compassionate use of clinical trial drugs is a potential way in which patients obtain research drugs when they are suffering from serious diseases or life-threatening diseases that cannot be effectively treated with marketed drugs.As research drugs are not approved into the market,evidence about their safety and efficacy is lacking.In order to ensure the safety of subjects,ethical committees need to perform their duties by conducting strict examination of treatments.

Key words: expanded access, compassionate use, clinical trials

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