医疗机构临床试验药物同情用药中国管理共识(2026)

  • 摘要: 依据2019年修订的《中华人民共和国药品管理法》和2026年实施的《中华人民共和国药品管理法实施条例》,由北京协和医院牵头,组织医疗卫生政策专家、临床医生、药师、方法学专家、伦理学专家和产业代表等相关领域专家,根据世界卫生组织手册和中华医学会推荐的共识制定过程,制定了《医疗机构临床试验药物同情用药中国管理共识(2026)》。其为我国第一部关于临床试验药物同情用药的管理共识,针对同情用药的适用条件、适用范围、患者人群、相关方的责任、申请和审查要点、患者知情同意、风险防控、费用承担等8个问题形成了19条推荐意见。本共识旨在规范医疗机构内部临床试验药物同情用药的临床实践,以期提高我国医疗机构对该问题的认识,改善急需治疗的危重患者的临床需求,为建立标准化的同情用药管理程序提供建议和参考。

     

    Abstract: In accordance with the Pharmaceutical Administration Law of the People's Republic of China revised in 2019 and the Implementing Regulations of the Pharmaceutical Administration Law of the People's Republic of China effective in 2026, Peking Union Medical College Hospital led the development of The Chinese Management Consensus on Compassionate Use of Investigational New Drugs in Medical Institutions (2026). This consensus was formulated by convening a multidisciplinary panel of experts, including health policy specialists, clinicians, pharmacists, methodologists, ethicists, and industry representatives, following the consensus development process recommended by the World Health Organization handbook and the Chinese Medical Association. As the first management consensus in China specifically addressing compassionate use of investigational drugs, this document provides 19 recommendations across eight key domains:eligibility criteria for compassionate use, scope of application, target patient populations, responsibilities of relevant stakeholders, key points for application and review, patient informed consent, risk prevention and control, and cost-bearing arrangements. This consensus aims to standardize the clinical practice of compassionate use of investigational drugs within medical institutions, enhance awareness of this issue among healthcare institutions in China, address the clinical needs of critically ill patients requiring urgent treatment, and provide recommendations and references for the establishment of standardized compassionate use management procedures.

     

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