公共资助药品的行业价格保证:从大流行病及以后的 NextGen 项目中学习。

IF 2.5 2区 哲学 Q1 ETHICS Journal of Law and the Biosciences Pub Date : 2024-09-11 eCollection Date: 2024-07-01 DOI:10.1093/jlb/lsae019
Holly Fernandez Lynch, Rena M Conti, Jorge L Contreras
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引用次数: 0

摘要

公共资助药品的可负担性一直是人们长期关注的问题。2023 年,拜登政府在这方面采取了若干措施,包括在美国生物医学高级研究与发展局(BARDA)与再生元制药公司(Regeneron Pharmaceuticals, Inc.该协议包括一项 "最惠国"(MFN)条款,Regeneron 同意,利用 BARDA 资金开发的某些产品在美国的商业上市价格不得超过其在全球同类市场的零售价格。战略准备与响应管理局(ASPR)在随后的协议中也加入了类似的条款,并承诺这将成为一项新的标准。即使不局限于备灾领域,政府出资方和采购方也可以考虑在未来的合同中加入类似条款,尤其是考虑到 Regeneron 协议及其后续条款被誉为 "开创性"。然而,仔细研究一下就会发现,我们有理由持怀疑态度。Regeneron 的最惠国条款在涵盖的购买者和参照国、价格和条件方面存在若干漏洞。我们对协议条款进行了描述,这些条款可能会在具有法律意义的价格限制和仅仅是装点门面之间产生差异。我们的批判性分析为今后提高利用公共资金开发的医疗技术的可负担性提供了重要启示。
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Industry price guarantees for publicly funded medicines: learning from Project NextGen for pandemics and beyond.

The affordability of publicly funded medicines has been a longstanding concern. In 2023, the Biden administration took several steps on this front, including incorporation of a price constraint in an agreement between the US Biomedical Advanced Research and Development Authority (BARDA) and Regeneron Pharmaceuticals, Inc. to develop a new COVID-19 monoclonal antibody. The agreement included a 'Most Favored Nation' (MFN) clause in which Regeneron agreed that the US commercial list price of certain products developed using BARDA funding would not exceed their retail price in comparable global markets. The Administration for Strategic Preparedness and Response (ASPR) included similar language in subsequent agreements, with a promise that this would become a new standard. Even beyond the preparedness context, government funders and purchasers might consider incorporating similar clauses in future contracts, especially given that the Regeneron agreement and its progeny have been praised as 'groundbreaking.' Yet a closer look reveals cause for skepticism. Regeneron's MFN clause includes several loopholes related to covered purchasers and reference countries, prices, and conditions. We describe agreement terms that can make the difference between legally meaningful price constraints and mere window dressing. Our critical analysis offers important lessons for future efforts to improve the affordability of medical technology developed with public funds.

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来源期刊
Journal of Law and the Biosciences
Journal of Law and the Biosciences Medicine-Medicine (miscellaneous)
CiteScore
7.40
自引率
5.90%
发文量
35
审稿时长
13 weeks
期刊介绍: The Journal of Law and the Biosciences (JLB) is the first fully Open Access peer-reviewed legal journal focused on the advances at the intersection of law and the biosciences. A co-venture between Duke University, Harvard University Law School, and Stanford University, and published by Oxford University Press, this open access, online, and interdisciplinary academic journal publishes cutting-edge scholarship in this important new field. The Journal contains original and response articles, essays, and commentaries on a wide range of topics, including bioethics, neuroethics, genetics, reproductive technologies, stem cells, enhancement, patent law, and food and drug regulation. JLB is published as one volume with three issues per year with new articles posted online on an ongoing basis.
期刊最新文献
The new EU-US data protection framework's implications for healthcare. The new regulation of non-medical neurotechnologies in the European Union: overview and reflection. Implementing the human right to science in the context of health: introduction to the special issue. Biosimilar approval pathways: comparing the roles of five medicines regulators. Industry price guarantees for publicly funded medicines: learning from Project NextGen for pandemics and beyond.
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