Back to Search Start Over

Exploring the opportunities for alignment of regulatory postauthorization requirements and data required for performance-based managed entry agreements

Authors :
Jonathan Lind Martinsson
Peter Arlett
Rick A. Vreman
Martin Wenzl
Inneke van de Vijver
Roisin Adams
Anna Nachtnebel
Lonneke Timmers
Hans-Georg Eichler
Einar Andreassen
Suzannah Chapman
Elias Pean
Tove Ragna Reksten
Guido Rasi
Wim G. Goettsch
Marc Van de Casteele
Jordi Llinares-Garcia
Afd Pharmacoepi & Clinical Pharmacology
Pharmacoepidemiology and Clinical Pharmacology
Source :
International Journal of Technology Assessment in Health Care, 37(1), 1. Cambridge University Press
Publication Year :
2021
Publisher :
Cambridge University Press (CUP), 2021.

Abstract

Performance-based managed entry agreements (PB-MEAs) might allow patient access to new medicines, but practical hurdles make competent authorities for pricing and reimbursement (CAPR) reluctant to implement PB-MEAs. We explored if the feasibility of PB-MEAs might improve by better aligning regulatory postauthorization requirements with the data generation of PB-MEAs and by active collaboration and data sharing. Reviewers from seven CAPRs provided structured assessments of the information available at the European Medicines Agency (EMA) Web site on regulatory postauthorization requirements for fifteen recently authorized products. The reviewers judged to what extent regulatory postauthorization studies could help implement PB-MEAs by addressing uncertainty gaps. Study domains assessed were: patient population, intervention, comparators, outcomes, time horizon, anticipated data quality, and anticipated robustness of analysis. Reviewers shared general comments about PB-MEAs for each product and on cooperation with other CAPRs. Reviewers rated regulatory postauthorization requirements at least partly helpful for most products and across domains except the comparator domain. One quarter of responses indicated that public information provided by the EMA was insufficient to support the implementation of PB-MEAs. Few PB-MEAs were in place for these products, but the potential for implementation of PB-MEAs or collaboration across CAPRs was seen as more favorable. Responses helped delineate a set of conditions where PB-MEAs may help reduce uncertainty. In conclusion, PB-MEAs are not a preferred option for CAPRs, but we identified conditions where PB-MEAs might be worth considering. The complexities of implementing PB-MEAs remain a hurdle, but collaboration across silos and more transparency on postauthorization studies could help overcome some barriers. ispartof: International Journal Of Technology Assessment In Health Care vol:37 issue:e83 pages:1-11 ispartof: location:England status: Published online

Details

ISSN :
02664623
Database :
OpenAIRE
Journal :
International Journal of Technology Assessment in Health Care, 37(1), 1. Cambridge University Press
Accession number :
edsair.doi.dedup.....3b4f7d48d3f7dd1a95acfc3ddd658259