Use of Real-World Data and Real-World Evidence in Rare Disease Drug Development: A Statistical Perspective
- PMID: 39949314
- DOI: 10.1002/cpt.3576
Use of Real-World Data and Real-World Evidence in Rare Disease Drug Development: A Statistical Perspective
Abstract
Real-world data (RWD) and real-world evidence (RWE) have been increasingly used in medical product development and regulatory decision-making, especially for rare diseases. After outlining the challenges and possible strategies to address the challenges in rare disease drug development (see the accompanying paper), the Real-World Evidence (RWE) Scientific Working Group of the American Statistical Association Biopharmaceutical Section reviews the roles of RWD and RWE in clinical trials for drugs treating rare diseases. This paper summarizes relevant guidance documents and frameworks by selected regulatory agencies and the current practice on the use of RWD and RWE in natural history studies and the design, conduct, and analysis of rare disease clinical trials. A targeted learning roadmap for rare disease trials is described, followed by case studies on the use of RWD and RWE to support a natural history study and marketing applications in various settings.
© 2025 The Author(s). Clinical Pharmacology & Therapeutics © 2025 American Society for Clinical Pharmacology and Therapeutics.
References
-
- US Congress. 21st Century Cures Act. 114th Congress (2016).
-
- FDA. Framework for FDA's real‐world evidence program (U.S. Department of Health and Human Services, Food and Drug Administration, Silver Spring, Maryland, 2018).
-
- Jarow, J.P., LaVange, L. & Woodcock, J. Multidimensional evidence generation and FDA regulatory decision making: defining and using “real‐world” data. JAMA 318, 703–704 (2017).
-
- Feinberg, B.A., Gajra, A., Zettler, M.E., Phillips, T.D., Phillips Jr, E.G. & Kish, J.K. Use of real‐world evidence to support FDA approval of oncology drugs. Value Health 23, 1358–1365 (2020).
-
- Jasmanda, W., Wang, C., Toh, S., Pisa, F.E. & Bauer, L. Use of real‐world evidence in regulatory decisions for rare diseases in the United States– current status and future directions. Pharmacoepidemiol Drug Saf. 29, 1213–1218 (2020).
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
