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Updated: Jun 16, 2025

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ICH M12药物相互作用研究:努力实现全球趋同的总结
Kellie Reynolds1, Xinning Yang1, Sheila Annie Peters2
1U.S. Food and Drug Administration, Silver Spring, Maryland, USA.
Clinical pharmacology and therapeutics
|March 20, 2025
概括
ICH M12指南协调了全球药物相互作用 (DDI) 评估,重点是药理学DDI. 它为体外和临床研究提供了最新的建议,帮助风险管理策略.
科学领域:
- 药理学 药理学是指药理学的学科.
- 药物开发 药物开发
- 监管科学 监管科学
背景情况:
- 药物相互作用 (DDI) 在药物开发中存在重大风险.
- 协调DDI评估准则对于全球监管的一致性至关重要.
- 之前的指导方针在几个关键的DDI评估方面缺乏共识.
研究的目的:
- 描述ICH M12药物相互作用研究指南所涉及的主题.
- 在准则制定过程中突出广泛讨论和公众商的领域.
- 为药理动力学DDI评估提供最新的建议.
主要方法:
- 专家工作组 (EWG) 的合作和共识建设.
- 审查现有的区域指南和科学文献.
- 纳入公众商期间的反.
主要成果:
- 更新了体外DDI研究的标准,包括蛋白质结合和代谢物评估.
- 临床DDI研究的精细方法,如生物标志物和嵌套研究设计.
- 关于UGT介导DDI的预测建模和评估的指导.
结论:
- ICH M12指南为药理动力学DDI评估提供了一个协调的框架.
- 更新的建议加强了在药物开发过程中对DDI的预测和管理.
- 该指南旨在促进DDI评估方法的科学进步.
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