药物开发
工程伦理学
现代化理论
药品审批
食品药品监督管理局
风险分析(工程)
药物发现
立场文件
范式转换
业务
药品
管理科学
过程管理
政治学
计算机科学
补语(音乐)
药品管理局
医学
数据科学
伦理问题
职位(财务)
新兴技术
知识管理
梅德林
监管事务
作者
Xuekun Wu,Matthew A. Wu,James Zou,Nicole Kleinstreuer,J Wu
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-04-16
卷期号:392 (6796): 371-378
被引量:3
标识
DOI:10.1126/science.aeb0045
摘要
Despite unprecedented technological progress, most drug candidates continue to fail in clinical trials, reflecting a persistent gap between preclinical models and human biology. New approach methodologies (NAMs), by spanning human-derived cellular systems, microphysiological platforms, and artificial intelligence, offer a paradigm shift in human-centric drug development and biomedical research. Recent regulatory reforms, such as the US Food and Drug Administration (FDA) Modernization Act 3.0, have begun to position NAMs as a complement to or replacement for animal testing. This Review synthesizes emerging biological and computational NAMs and examines how their integration is reshaping drug development. We also discuss regulatory and ethical frameworks enabling this transition and outline a roadmap for embedding human-based science in a predictive, efficient, and ethically grounded infrastructure of human-centered drug development.
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