中国药物警戒 ›› 2021, Vol. 18 ›› Issue (1): 47-51.
DOI: 10.19803/j.1672-8629.2021.01.09
马静, 高京宏, 刘春光*
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。
MA Jing, GAO Jinghong, LIU Chunguang*
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。
中图分类号:
马静, 高京宏, 刘春光. 拓展性同情使用临床试验用药制度的相关问题研究[J]. 中国药物警戒, 2021, 18(1): 47-51.
MA Jing, GAO Jinghong, LIU Chunguang. Issues Related to Expanded Access to Investigational Drugs for Compassionate Use[J]. Chinese Journal of Pharmacovigilance, 2021, 18(1): 47-51.
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