张忠兵, 王旸, 白玉. 抗体偶联药物研发及药学审评要点J. 药学学报, 2020,55(8): 1971-1977. doi: 10.16438/j.0513-4870.2020-0325
引用本文: 张忠兵, 王旸, 白玉. 抗体偶联药物研发及药学审评要点J. 药学学报, 2020,55(8): 1971-1977. doi: 10.16438/j.0513-4870.2020-0325
ZHANG Zhong-bing, WANG Yang, BAI Yu. Consideration of antibody drug conjugates development and regulationJ. Acta Pharmaceutica Sinica, 2020,55(8): 1971-1977. doi: 10.16438/j.0513-4870.2020-0325
Citation: ZHANG Zhong-bing, WANG Yang, BAI Yu. Consideration of antibody drug conjugates development and regulationJ. Acta Pharmaceutica Sinica, 2020,55(8): 1971-1977. doi: 10.16438/j.0513-4870.2020-0325

抗体偶联药物研发及药学审评要点

Consideration of antibody drug conjugates development and regulation

  • 摘要: 抗体偶联物(antibody drug conjugates,ADCs)兼具抗体的靶向性和小分子化合物的细胞毒性,目前已经成为抗肿瘤药物研发的热点之一。靶抗原、抗体、毒素、连接子或偶联方式的选择是影响ADCs药物开发成功的要素。本文介绍了ADCs药物在开发和结构设计方面需考虑的主要因素,以及在此类产品申报时药学技术审评的要点,希望能为研发单位开发ADCs药物提供参考。

     

    Abstract: Antibody drug conjugates (ADCs), as they combine the targetability of monoclonal antibody and cytotoxicity of small molecules, are a growing class of therapeutics for cancer. The key factor of ADCs development is the accurate selection of parameters including tumor target, monoclonal antibody, cytotoxic payload, and linkage strategy of antibody to payload. Here, we summarize the main elements in the structural design and the development of ADCs, as well as the regulatory consideration of product manufacturing and control, which would be helpful for the research and development of ADCs.

     

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