Leveraging Real-World Data in Safety Signal Assessment.

IF 2 4区 医学 Q4 MEDICAL INFORMATICS
Vaishali Patadia, Katrin Manlik, Geoffrey Gipson, Jenna C Willis, Ruth Namuyinga, Rachel McDermott, Anita Shaw, Mary K Miller, Julius Asubonteng, Negar Golchin, Stephanie von Klot
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Abstract

Purpose: TransCelerate BioPharma surveyed its member biopharmaceutical companies to understand current practices and identify opportunities to complement safety signal assessment with rapid real-world data (RWD) analysis.

Methods: A voluntary 30-question questionnaire regarding the use of RWD in safety signal assessment was disseminated to subject matter experts at all TransCelerate member companies in July 2022. Responses were blinded, aggregated, summarized, and presented.

Results: Eighteen of 20 member companies provided responses to the questionnaire. Sixteen (89%) companies reported actively leveraging RWD in their signal assessment processes. Of 18 respondent companies, 8 (44%) routinely use rapid approaches to RWD analysis, 7 (39%) utilize rapid RWD analysis non-routinely or in a pilot setting, 2 (11%) are considering using rapid RWD analysis, and 1 (6%) has no plans to use rapid RWD analysis for their signal assessment. Most companies reported that RWD adds context to and improves quality of signal assessments. To conduct RWD analysis for signal assessment, 16 of 17 (94%) respondent companies utilize or plan to utilize internally available data, 8 (47%) utilize both internal and external data, and 3 (18%) utilize data networks. Respondents identified key challenges to rapidly performing RWD analyses, including data access/availability, time for analysis execution, and uncertainties regarding acceptance of minimal or non-protocolized approaches by health authorities.

Conclusion: Biopharmaceutical companies reported that they see value in the use of rapid RWD analyses for complementing signal assessments. Future work is recommended to offer a framework and process for use of rapid use of RWD analyses in signal assessment.

Abstract Image

在安全信号评估中利用真实世界数据。
目的:TransCelerate BioPharma 对其成员生物制药公司进行了调查,以了解当前的做法,并确定利用快速真实世界数据(RWD)分析对安全信号评估进行补充的机会:2022 年 7 月,我们向 TransCelerate 所有成员公司的主题专家分发了一份有关在安全信号评估中使用 RWD 的 30 个问题的自愿问卷。调查结果:20 家成员公司中有 18 家提供了答复:20 家成员公司中有 18 家对问卷进行了回复。16家公司(89%)表示在信号评估流程中积极利用了 RWD。在 18 家受访公司中,8 家公司(44%)例行使用快速 RWD 分析方法,7 家公司(39%)非例行或在试点环境中使用快速 RWD 分析方法,2 家公司(11%)正在考虑使用快速 RWD 分析方法,1 家公司(6%)没有计划在信号评估中使用快速 RWD 分析方法。大多数公司报告说,RWD 增加了信号评估的背景,提高了信号评估的质量。为进行信号评估的 RWD 分析,17 家受访公司中有 16 家(94%)利用或计划利用内部可用数据,8 家(47%)利用内部和外部数据,3 家(18%)利用数据网络。受访者指出了快速执行 RWD 分析所面临的主要挑战,包括数据访问/可用性、执行分析所需的时间,以及卫生当局是否接受最小化或非协议化方法的不确定性:生物制药公司表示,他们认为使用快速 RWD 分析对信号评估具有补充价值。建议今后开展工作,为在信号评估中快速使用 RWD 分析提供框架和流程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Therapeutic innovation & regulatory science
Therapeutic innovation & regulatory science MEDICAL INFORMATICS-PHARMACOLOGY & PHARMACY
CiteScore
3.40
自引率
13.30%
发文量
127
期刊介绍: Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health. The focus areas of the journal are as follows: Biostatistics Clinical Trials Product Development and Innovation Global Perspectives Policy Regulatory Science Product Safety Special Populations
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