Abstract

BackgroundThe 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.ObjectivesThe aim of this evaluation is to identify factors influencing the results of the AMNOG price negotiation process.MethodsThe 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).ResultsUntil 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.ConclusionsAlthough 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.

Highlights

  • The AMNOG regulation, introduced in 2011 in Germany, changed the game for new drugs

  • Until December 2015, manufacturers and the Gesetzliche Krankenversicherung (GKV)-SV finalized 96 negotiations in 193 therapeutic areas, based on assessment conducted by the Gemeinsamer Bundesausschuss (GBA)

  • The GBA has granted an additional benefit to 100/193 drug innovations

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Summary

Introduction

The AMNOG regulation, introduced in 2011 in Germany, changed the game for new drugs. 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). Pharmaceutical companies are obliged by law to submit a dossier to the Federal Joint Committee (Gemeinsamer Bundesausschuss, GBA) in order to prove a patientrelevant medical benefit in mortality, morbidity, and health-related quality of life (HRQoL). The GBA is the decision-making body of the joint self-governing board of stakeholders in healthcare (physicians, dentists, hospitals and sickness funds) in the German Statutory Health Insurance (Gesetzliche Krankenversicherung, GKV). A ruling on additional benefit for a specific compound by the GBA (appraisal) is based on the overall assessment of the evidence presented in the dossier for effects on mortality, morbidity, and HRQoL. Sometimes a manufacturer decides not to submit a dossier and accepts a rating of no additional benefit from the beginning

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