Literature DB >> 27987628

Arbitration Board Setting Reimbursement Amounts for Pharmaceutical Innovations in Germany When Price Negations between Payers and Manufacturers Fail: An Empirical Analysis of 5 Years' Experience.

Saskia Ludwig1, Charalabos-Markos Dintsios2.   

Abstract

BACKGROUND: In Germany, an arbitration board is setting reimbursement amounts for drug innovations when price negations between payers and manufacturers fail.
OBJECTIVE: To empirically analyze all arbitrations since the reform of Germany's Act to Reorganize the Pharmaceuticals' Market in the Statutory Health Insurance System came into effect.
METHODS: All available relevant documents up to January 2016 were screened and the identified contentious issues between the negotiation parties extracted. Reimbursement requests of both the negotiating parties and the arbitrations were transformed into a comparable format on the basis of defined daily doses and then contrasted among each other.
RESULTS: In the given period, 16 arbitrations took place. The arbitration board is implementing the same criteria used in the negotiations between manufacturers and payers. Almost all arbitrations dealt with generic appropriate comparative therapies. Reimbursement amounts set by arbitration were on average 38.4% less than the mean of negotiation parties' requests (69.2% less than the manufacturers' requests). The corresponding prescription volumes were arranged rather centrally. All but one arbitration refer to a 1-year contract period. The arbitration board rarely decided on further technical contentious points. Hence, no heuristics referring to them were derivable.
CONCLUSIONS: There is some evidence for a quasi-algorithmic approach of the arbitration board, even though it is legally determined that it has to decide while taking the peculiar conditions of each case into due consideration, including the characteristics of the respective therapeutic area. The balance of interests proved to be within a very narrow space albeit it concerns in principle discretionary decisions. Thus, the purpose of arbitration seems not to be achieved sufficiently.
Copyright © 2016 International Society for Pharmacoeconomics and Outcomes Research (ISPOR). Published by Elsevier Inc. All rights reserved.

Keywords:  AMNOG; arbitration board; early benefit assessment; price negotiations; reimbursement amount

Mesh:

Year:  2016        PMID: 27987628     DOI: 10.1016/j.jval.2016.05.016

Source DB:  PubMed          Journal:  Value Health        ISSN: 1098-3015            Impact factor:   5.725


  4 in total

1.  Determinants of Orphan Drug Prices in Germany.

Authors:  Franziska Worm; Charalabos-Markos Dintsios
Journal:  Pharmacoeconomics       Date:  2020-04       Impact factor: 4.981

2.  Predictors of negotiated prices for new drugs in Germany.

Authors:  Afschin Gandjour; Sofia Schüßler; Thomas Hammerschmidt; Charalabos-Markos Dintsios
Journal:  Eur J Health Econ       Date:  2020-05-25

3.  Different interpretation of additional evidence for HTA by the commissioned HTA body and the commissioning decision maker in Germany: whenever IQWiG and Federal Joint Committee disagree.

Authors:  C M Dintsios; F Worm; J Ruof; M Herpers
Journal:  Health Econ Rev       Date:  2019-12-17

4.  How Far is Germany From Value-Based Pricing 10 Years After the Introduction of AMNOG?

Authors:  Charalabos-Markos Dintsios; Nadja Chernyak
Journal:  Appl Health Econ Health Policy       Date:  2021-12-29       Impact factor: 3.686

  4 in total

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