Author:
Patadia Vaishali,Manlik Katrin,Gipson Geoffrey,Willis Jenna C.,Namuyinga Ruth,McDermott Rachel,Shaw Anita,Miller Mary K.,Asubonteng Julius,Golchin Negar,von Klot Stephanie
Abstract
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.
Publisher
Springer Science and Business Media LLC
Reference16 articles.
1. World Health Organization. Pharmacovigilance: Ensuring the Safe Use of Medicines. https://apps.who.int/iris/bitstream/handle/10665/68782/WHO_EDM_2004.8.pdf. Accessed 25 April 2023.
2. Guideline on good pharmacovigilance practices (GVP) Module IX—Signal management (Rev 1) 2017. https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-good-pharmacovigilance-practices-gvp-module-ix-signal-management-rev-1_en.pdf
3. Lavertu A, Vora B, Giacomini KM, Altman R, Rensi S. A new era in pharmacovigilance: toward real-world data and digital monitoring. Clin Pharmacol Ther. 2021;109(5):1197–202. https://doi.org/10.1002/cpt.2172.
4. Framework for FDA’s Real-World Evidence Program. 2018. https://www.fda.gov/media/120060/download
5. Rapid Signal Assessment Using Real World Data. TransCelerate BioPharma Inc. https://www.transceleratebiopharmainc.com/initiatives/rapid-signal-assessment-using-real-world-data
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