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      From Indication-Based Pricing to Blended Approach: Evidence on the Price and Reimbursement Negotiation in Italy

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          Abstract

          Background

          New indications for existing medicines are increasing over time. In most countries, drug pricing and reimbursement conditions are renegotiated every time a new indication is approved. There is a growing interest in the price negotiation model for new indications, specifically comparing an indication-based versus blended approach. However, little evidence currently exists regarding the complexity of these negotiations and their impact on actual prices. Italy has recently transitioned from an indication-based approach to a blended price model. This study aims to measure the impact of price and reimbursement negotiation of new indications on discounts (i.e. actual prices) and on the negotiation duration, used as a proxy of its complexity.

          Methods

          We considered new indications approved through a European centralized procedure from January 2013 to March 2022 for which the price and reimbursement status was approved in Italy between January 2015 and March 2022, amounting to 52 new indications. Data on the timeframe of the Italian price and reimbursement process and its phases were obtained from publicly available sources. Discounts for the first indication and their subsequent increases for new indications were estimated by comparing ex-factory prices and tendered prices. To calculate p-values, we employed the Mann–Whitney test, and multiple regression models were utilized to examine correlations between negotiation time and the characteristics of the medicines.

          Results

          The mean time to reimbursement was 603 days, in contrast to 583 days for the first launch. Price negotiation took longer for rare diseases, cancer drugs, and in case of therapies with minor added therapeutic value. On average, the additional discount (on top of discounts for prior indications) was 13%, significantly lower than the mean discount for the first indications approved (24.9%). The discounts increment was lower, but negotiation took longer if a Managed Entry Agreement accompanied the final agreement. Additionally, discounts have increased over the years.

          Conclusion

          The negotiation for new indications takes longer than the first one, and provides, on average, an additional discount of 13%. While our findings bear the potential for significant policy implications, they necessitate prudent interpretation due to a limited number of observations. The increasing trend in additional discounts over time applied to all indications in recent negotiations, may suggest a descending trend of value for new indications and a shift from an indication-based pricing approach to a blended model. Otherwise, budget impact considerations might have outweighed a value-based approach in the recent negotiations. If so, two potential options for restoring a value-based approach are returning to an indication-based pricing or giving explicit and higher weight to value within a blended model.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s41669-023-00467-2.

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          Most cited references15

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          Implementation of Value-based Pricing for Medicines

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            The Use of Risk-Sharing Contracts in Healthcare: Theoretical and Empirical Assessments

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              Is Open Access

              The Evolution of AIFA Registries to Support Managed Entry Agreements for Orphan Medicinal Products in Italy

              Italy has a well-established prominent system of national registries to support managed entry agreements (MEAs), monitoring innovative medicinal products (MPs) with clinical as well as economic uncertainties to ensure appropriate use and best value for money. The technological architecture of the registries is funded by pharmaceutical companies, but fully governed by the national medicines agency (AIFA). A desktop analysis was undertaken of data over a 15-year timeframe of all AIFA indication-based registries and associated EMA information. The characteristics of registries were evaluated, comparing orphan MPs vs. all MPs exploring cancer and non-cancer indications. OMP (orphan medicinal product) registries’ type vs. AIFA innovation status and EMA approval was reviewed. Of the 283 registries, 182 are appropriateness registries (35.2% relate to OMPs, with an almost equal split of cancer vs. non-cancer for OMPs and MPs), 35 include financial-based agreements [20% OMPs (2 non-cancer, 5 cancer)], and 60 registries are payment by result agreements [23.3% OMPs (4 non-cancer, 10 cancer)]. Most OMPs (53/88) came through the normal regulatory route. With the strengthening of the system for evaluation of innovation, fewer outcomes-based registries have been instigated. AIFA has overcome many of the challenges experienced with MEA through developing an integrated national web-based data collection system: the challenge that remains for AIFA is to move from using the system for individual patient decisions about treatment to reviewing the wealth of data it now holds to optimize healthcare.
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                Author and article information

                Contributors
                elvioemanuele.rossini01@gmail.com
                Journal
                Pharmacoecon Open
                Pharmacoecon Open
                PharmacoEconomics Open
                Springer International Publishing (Cham )
                2509-4262
                2509-4254
                16 January 2024
                16 January 2024
                March 2024
                : 8
                : 2
                : 251-261
                Affiliations
                [1 ]GRID grid.518889.5, Market Access, , Pharmalex Italy Spa, ; Milan, Italy
                [2 ]Bicocca Applied Statistics Center (B-ASC), Università degli Studi di Milano-Bicocca, ( https://ror.org/01ynf4891) Milan, Italy
                [3 ]GRID grid.518889.5, Patient Access, , Pharmalex Italy Spa, ; Milan, Italy
                [4 ]GRID grid.16563.37, ISNI 0000000121663741, Department of Pharmaceutical Sciences, , Università del Piemonte Orientale, ; Novara, Italy
                Author information
                http://orcid.org/0000-0003-3928-8550
                Article
                467
                10.1007/s41669-023-00467-2
                10883902
                38228997
                a8fd9d2d-fee5-486e-bc44-51521d84742a
                © The Author(s) 2023, corrected publication 2024

                Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 14 December 2023
                Categories
                Original Research Article
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                © Springer Nature Switzerland AG 2024

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