Key result
Real-world data can expedite regulatory decisions for antihypertensive fixed-dose combinations despite EU legislative uncertainty.
Why the study?
This review addresses the complexity surrounding the use of real-world data and real-world evidence in drug repurposing, such as antihypertensive fixed-dose combinations.
Real-world data and evidence offer a transformative opportunity to expedite regulatory decisions for antihypertensive fixed-dose combinations, though EU regulatory acceptance needs advancement.
Answers are grounded in this paper and cite their sources.
RWD/RWE may aid antihypertensive FDC repurposing; leaves open standardization and regulatory acceptance.
PURPOSE: Real-world data (RWD) and real-world evidence (RWE) offer significant potential for clinical development and clinical evidence generation. This review addresses the complexity surrounding the use of RWD and RWE in drug repurposing, such as antihypertensive fixed-dose combinations of known compounds from the 5 major pharmacological classes. METHODS: We performed a narrative review examining RWD and RWE use in the development and registration of antihypertensive fixed-dose combinations, covering their role as examples of value-added medicines, regulatory policies, scientific perceptions, application in hypertension research, regulatory use cases, and economic factors. FINDINGS: Well-designed RWE studies can yield clinical performance data comparable with findings of randomized controlled trials while addressing certain limitations. However, current European Union (EU) legislation regarding the usability of RWD and RWE is conservative and needs to be updated. Divergent opinions among EU member states pose uncertainty and risk for industry in marketing authorization applications involving RWD and RWE. IMPLICATIONS: Real-world data and RWE offer a transformative opportunity through data sourced beyond traditional clinical trials. This approach can expedite regulatory decisions, reduce development timelines and costs, and accelerate the delivery of valuable therapies to patients. Discussions at the centralized EU regulatory level are needed to recognize and accept RWE as valid for demonstrating clinical efficacy and safety.
No takes yet. Share an insight, caveat, or question.
Mogielnicki et al. (2025) conducted a review in Hypertension. Real-world data and real-world evidence was evaluated. Real-world data and evidence can expedite regulatory decisions for antihypertensive fixed-dose combinations, though current conservative EU legislation poses uncertainty for industry applications.
Synapse has enriched 10 related papers. Consider them for comparative context: