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从非临床到临床计划的转化挑战:案例研究示例
Deven Dandekar1, David B Hawver2, Deepa B Rao3
1Department of Toxicology, ExploR&D, Eli Lilly and Company, Indianapolis, IN, USA.
International journal of toxicology
|November 19, 2025
概括
将非临床数据转化为临床药物开发是复杂的. 案例研究有助于提高管理更安全,更有效的候选药物的翻译挑战的技能.
科学领域:
- 药理学和毒理学 药理学和毒理学
- 药物开发科学 药物开发科学
背景情况:
- 药物发现和开发是一个漫长而昂贵的过程 (10-15年,1-20亿美元).
- 关于将非临床数据转化为临床试验设计的指南有限.
- 非临床研究对于确定首次对人体进行试验的安全剂量范围至关重要.
研究的目的:
- 解决将非临床发现转化为临床药物开发的挑战.
- 提高在药物开发计划中遇到的翻译障碍的管理技能.
- 提供案例研究示例,以加强非临床到临床过渡的管理.
主要方法:
- 利用案例研究来说明药物开发中的翻译挑战.
- 专注于整合来自各种药理相关物种的数据.
- 研究了病理学家,ADME科学家,生物学家和临床医生之间跨职能合作的重要性.
主要成果:
- 确定了候选药物失败的常见原因,包括对转化过程的不充分理解.
- 强调了有效整合不同物种数据的影响.
- 证明了在慢性毒理学研究中安全边际如何被侵蚀.
结论:
- 有效地将非临床数据转化为临床设计对于成功的药物开发至关重要.
- 跨职能合作对于应对翻译挑战至关重要.
- 案例研究为改进翻译策略提供了有价值的学习机会.
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