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Considerations for Clinical Review of Cellular Therapy Products: Perspectives of the China Food and Drug Administration Center for Drug Evaluation

机译:细胞治疗产品临床审查的考虑因素:中国食品和药物毒品评估中心的视角

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摘要

With increasing numbers of technical developments and clinical studies, pioneering cellular/gene therapies are now available that could cure life-threatening disease. Cellular/gene therapy products are broad-ranging and complicated, and thereby bring challenges for clinical review by regulatory agencies. This review discusses principles for the clinical review of cellular therapy products, including protection of clinical trial populations, pharmacodynamics, pharmacokinetics, dose evaluation, clinical efficacy, clinical safety, and risk-management plans. Based on these principles, key points in the clinical review of chimeric antigen receptor T-cell therapy are also discussed.
机译:随着越来越多的技术开发和临床研究,现在可以治愈危及生命的疾病的开创性细胞/基因疗法。 细胞/基因治疗产品是广泛的和复杂的,因此对监管机构临床审查带来挑战。 本综述讨论了细胞治疗产品临床审查的原则,包括保护临床试验群体,药效学,药代动力学,剂量评估,临床疗效,临床安全和风险管理计划。 基于这些原则,还讨论了嵌合抗原受体T细胞疗法的临床审查的关键点。

著录项

  • 来源
    《Human gene therapy》 |2018年第2期|共7页
  • 作者单位

    Office of Clinical Evaluation of Biological Products Center for Drug Evaluation China Food and;

    Office of Clinical Evaluation of Biological Products Center for Drug Evaluation China Food and;

    Office of Clinical Evaluation of Biological Products Center for Drug Evaluation China Food and;

    Office of Clinical Evaluation of Biological Products Center for Drug Evaluation China Food and;

    Center for Drug Evaluation China Food and Drug Administration Beijing China.;

    Office of Clinical Evaluation of Biological Products Center for Drug Evaluation China Food and;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 治疗学;
  • 关键词

    cellular/gene therapy products; clinical review; CAR T-cell therapy; risk management;

    机译:细胞/基因治疗产品;临床评论;汽车T细胞疗法;风险管理;

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