综合安全评估规划如何支持调查性新药安全报告决策
Barbara A Hendrickson1, Cynthia McShea2, Greg Ball3
1Department of Pediatrics, University of Chicago, Chicago, IL, 60637, USA. bhendric@bsd.uchicago.edu.
Therapeutic innovation & regulatory science
|March 30, 2024
概括
总体安全评估计划 (ASAP) 帮助赞助商满足FDA关于总体安全报告的指导. 它概述了独立安全数据审查和报告决策的流程.
科学领域:
- 临床试验的安全性
- 药物监督 药物监督 药物监督
- 监管科学是一种监管科学.
背景情况:
- 美国食品和药物管理局于2021年6月发布了关于发起人负责调查新药 (IND) 安全报告的指导草案.
- 该指南强调,需要为总体安全评估制定一份记录的计划.
研究的目的:
- 将综合安全评估计划 (ASAP) 作为满足FDA2021年指导期望的方法.
- 详细说明ASAP如何支持IND总体安全报告决策以及独立评估实体的作用.
主要方法:
- 讨论了药物信息协会-美国统计学会工作组提出的ASAP框架.
- 探索独立评估实体对安全数据无遮掩审查的策略.
- 倡导制定一份宪章,定义评估实体的职责.
主要成果:
- 该ASAP为总体安全评估和报告提供了一个结构化的方法.
- 将ASAP与安全监督计划 (SSP) 附件和评估实体章程相结合,可以促进合规.
- 建立了监测临床试验安全数据和做出IND安全报告决策的明确流程.
结论:
- 实施ASAP,以及SSP附录和评估实体章程,使赞助商能够满足FDA对综合IND安全报告的要求.
- 定义的流程可以加强对临床试验安全数据的监测,并支持明智的报告决策.
- 这种方法确保了强有力的安全监督和监管合规性.
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