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Determining the societal value of a prospective drug for ME/CFS in Germany

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  • Afschin Gandjour

Abstract

Background: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) imposes a substantial societal and economic burden. The aim of this study is to ascertain the optimal level of public research and development (R&D) investment in Germany for a prospective drug, given the pressing need for effective treatments. Methods: This study calculates the societal value from a German perspective by integrating health and economic outcomes in the context of public R&D investment for ME/CFS. It considers factors such as direct medical costs, productivity loss, and the effectiveness of a prospective drug. Results: The anticipated introduction of a prospective drug is estimated to yield a quality-adjusted life year (QALY) gain of approximately 29,000 and a societal value of about €2.6 billion. The optimal R&D investment in Germany is estimated at €676 million, which represents about a quarter of the total investment required to bring a significant drug to market, considering diminishing returns and market constraints. Results were confirmed in the sensitivity analysis. Conclusions: The study concludes that a coordinated international approach is imperative to address the funding and market size limitations effectively in developing treatments for ME/CFS and to realize the substantial societal and economic benefits.

Suggested Citation

  • Afschin Gandjour, 2024. "Determining the societal value of a prospective drug for ME/CFS in Germany," PLOS ONE, Public Library of Science, vol. 19(7), pages 1-11, July.
  • Handle: RePEc:plo:pone00:0307086
    DOI: 10.1371/journal.pone.0307086
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    References listed on IDEAS

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    1. Gandjour, Afschin, 2018. "Underuse of innovative medicines in Germany: A justification for government intervention?," Health Policy, Elsevier, vol. 122(12), pages 1283-1286.
    2. Michael Falk Hvidberg & Louise Schouborg Brinth & Anne V Olesen & Karin D Petersen & Lars Ehlers, 2015. "The Health-Related Quality of Life for Patients with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (ME/CFS)," PLOS ONE, Public Library of Science, vol. 10(7), pages 1-16, July.
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