Adopting a Framework for Rapid Real-World Data Analyses in Safety Signal Assessment

被引:0
|
作者
Wang, Lu [1 ]
Golchin, Negar [2 ]
von Klot, Stephanie [3 ]
Salinas, Claudia A. [4 ]
Manlik, Katrin [5 ]
Patadia, Vaishali [6 ]
Miller, Mary K. [7 ]
Asubonteng, Julius [8 ]
McDermott, Rachel [9 ]
Barberio, Julie [10 ]
Gipson, Geoffrey [1 ]
机构
[1] Pharmaceut Co Johnson & Johnson, Janssen Res & Dev LLC, 200 Tournament Dr, Horsham, PA 19044 USA
[2] BMS, New York, NY USA
[3] Boehringer Ingelheim Int GmbH, Ingelheim, Germany
[4] Eli Lilly & Co, Indianapolis, IN USA
[5] Bayer AG, Berlin, Germany
[6] Amgen Inc, Thousand Oaks, CA USA
[7] Genentech Inc, South San Francisco, CA USA
[8] Regeneron, Tarrytown, NY USA
[9] Shionogi, Osaka, Japan
[10] Sanofi, Cambridge, MA USA
关键词
Real-world data (RWD); Safety signal assessment; Pharmacovigilance; Transcelerate; Minimal protocol; Rapid data analysis;
D O I
10.1007/s43441-024-00694-7
中图分类号
R-058 [];
学科分类号
摘要
The expanding availability of real-world data (RWD) has led to an increase in both the interest and possibilities for using this information in postmarketing safety analyses and signal management. While there is enormous potential value from the safety insights generated through RWD, the analysis preparation, execution, and communication required to reliably deliver the evidence can be time consuming. Since the safety signal assessment process is a regulated and timebound process, any supporting RWD analyses require a rapid turnaround of well-designed and informative results. To address this challenge, a TransCelerate BioPharma working group was formed and developed a framework to help teams responsible for safety signal assessment overcome the challenges of working with RWD rapidly to deliver analyses within regulatory timelines. Here, a previously performed safety assessment was evaluated within the context of the developed framework to illustrate how the framework may be adopted in practice.
引用
收藏
页码:1014 / 1022
页数:9
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