2021
DOI: 10.1017/s026646232100057x
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Exploring the opportunities for alignment of regulatory postauthorization requirements and data required for performance-based managed entry agreements

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 Europ… Show more

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Cited by 13 publications
(9 citation statements)
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References 10 publications
(22 reference statements)
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“…The discrepancy between perceived and documented value can be addressed through the implementation of managed entry agreements, as evidenced by the increasing adoption of such agreements ( Jommi et al, 2020 ; Efthymiadou and Kanavos, 2022 ). The complexity associated with managed entry agreement implementation remains a challenge and contributes to extended time frames for the final reimbursement decision ( Kang et al, 2020 ; Eichler et al, 2021 ; Fens et al, 2021 ). To optimize the utilization of managed entry agreements, it is essential to incorporate them into the pricing strategies of pharmaceutical companies.…”
Section: Discussionmentioning
confidence: 99%
“…The discrepancy between perceived and documented value can be addressed through the implementation of managed entry agreements, as evidenced by the increasing adoption of such agreements ( Jommi et al, 2020 ; Efthymiadou and Kanavos, 2022 ). The complexity associated with managed entry agreement implementation remains a challenge and contributes to extended time frames for the final reimbursement decision ( Kang et al, 2020 ; Eichler et al, 2021 ; Fens et al, 2021 ). To optimize the utilization of managed entry agreements, it is essential to incorporate them into the pricing strategies of pharmaceutical companies.…”
Section: Discussionmentioning
confidence: 99%
“…The momentum for outcome-based reimbursement models is strengthened by the ongoing initiative to enhance regulatory post-authorization requirements, especially in those cases where only conditional market authorization is granted for new medicines which respond to huge unmet medical needs with uncertain clinical value (43). Implementation of outcome-based reimbursement models is challenging, especially in resource constrained health care systems of lower income countries.…”
Section: Discussionmentioning
confidence: 99%
“…Recently, Eichler et al[ 9 ] explored the feasibility of OBAs by interviewing reviewers from seven competent authorities for pricing and reimbursement. The type of product that can be considered as an OBA is described as a novel treatment with easily measurable outcomes for an unmet medical need but with uncertainty regarding its budget-impact or clinical value.…”
Section: Discussionmentioning
confidence: 99%
“…Nonetheless, in situations where the price and budget-impact are the main issues, other financial agreements can be used such as discounts, budget-caps or price-volume agreements. In general, OBAs were not often the preferred option for payers due to practical hurdles including manufacturers’ unwillingness to collaborate, differences in perception of value and administrative workload[ 9 ].…”
Section: Discussionmentioning
confidence: 99%