Benefit assessment in Germany: implications for price discounts

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dc.identifier.uri http://dx.doi.org/10.15488/2648
dc.identifier.uri http://www.repo.uni-hannover.de/handle/123456789/2674
dc.contributor.author Theidel, Ulrike
dc.contributor.author Schulenburg, Johann-Matthias Graf von der
dc.date.accessioned 2018-01-19T12:03:38Z
dc.date.available 2018-01-19T12:03:38Z
dc.date.issued 2016
dc.identifier.citation Theidel, U.; von der Schulenburg, J.-M.: Benefit assessment in Germany: implications for price discounts. In: Health Economics Review 6 (2016), Nr. 1, 33. DOI: https://doi.org/10.1186/s13561-016-0109-3
dc.description.abstract Background: The AMNOG regulation, introduced in 2011 in Germany, changed the game for new drugs. Now, the industry is required to submit a dossier to the GBA (the central decision body in the German sickness fund system) to show additional benefit. After granting the magnitude of the additional benefit by the GBA, the manufacturer is entitled to negotiate the reimbursement price with the GKV-SV (National Association of Statutory Health Insurance Funds). The reimbursement price is defined as a discount on the drug price at launch. As the price or discount negotiations between the manufacturers and the GKV-SV takes place behind closed doors, the factors influencing the results of the negotiation are not known. Objectives: The aim of this evaluation is to identify factors influencing the results of the AMNOG price negotiation process. Methods: The analysis was based on a dataset containing detailed information on all assessments until the end of 2015. A descriptive analysis was followed by an econometric analysis of various potential factors (benefit rating, size of target population, deviating from appropriate comparative therapy and incorporation of HRQoL-data). Results: Until December 2015, manufacturers and the GKV-SV finalized 96 negotiations in 193 therapeutic areas, based on assessment conducted by the GBA. The GBA has granted an additional benefit to 100/193 drug innovations. Negotiated discount was significantly higher for those drugs without additional benefit (p= 0.030) and non-orphan drugs (p= 0.015). Smaller population size, no deviation from recommended appropriate comparative therapy and the incorporation of HRQoL-data were associated with a lower discount on the price at launch. However, neither a uni- nor the multivariate linear regression showed enough power to predict the final discount. Conclusions: Although the AMNOG regulation implemented binding and strict rules for the benefit assessment itself, the outcome of the discount negotiations are still unpredictable. Obviously, negotiation tactics, the current political situation and soft factors seem to play a more influential role for the outcome of the negotiations than the five hard and known factors analyzed in this study. Further research is needed to evaluate additional factors. eng
dc.language.iso eng
dc.publisher Heidelberg : Springer Verlag
dc.relation.ispartofseries Health Economics Review 6 (2016), Nr. 1
dc.rights CC BY 4.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.subject Health policy eng
dc.subject Market access eng
dc.subject Negotiation eng
dc.subject New substance eng
dc.subject Pharmaceuticals eng
dc.subject Rebate eng
dc.subject.ddc 610 | Medizin, Gesundheit ger
dc.title Benefit assessment in Germany: implications for price discounts eng
dc.type Article
dc.type Text
dc.relation.issn 21911991
dc.relation.doi https://doi.org/10.1186/s13561-016-0109-3
dc.bibliographicCitation.issue 1
dc.bibliographicCitation.volume 6
dc.bibliographicCitation.firstPage 33
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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