CHOICE Institute, School of Pharmacy, University of Washington, Seattle.
Curta, Inc., Seattle, WA.
J Manag Care Spec Pharm. 2024 Oct;30(10):1065-1072. doi: 10.18553/jmcp.2024.24104. Epub 2024 Jul 16.
Biologic therapies play a critical role in modern medical practice but also present challenges for payers, patients, and other stakeholders because of their high cost. Biosimilars can mitigate the cost pressures of reference biologic therapy because they are typically priced at least 25% lower, providing a means to administer cutting-edge biologic therapy while also managing cost of care. In fact, the US health care system has saved an estimated $23.6 billion from use of biosimilars. However, the market is still in a nascent phase of development, and early cost-saving successes are not guaranteed to persist unless sustainable market conditions are established. To better understand the perspectives of stakeholders about opportunities and threats to the sustainability of the US biosimilar market, a multistakeholder roundtable discussion was convened in December of 2023 and included health care payers, providers, self-insured employers, a manufacturer, and a biosimilar research and advocacy organization. The objective of this commentary, authored by the roundtable participants, is to posit specific opportunities and threats that stakeholders should consider to better facilitate sustainable biosimilar market conditions in the United States. We highlight key points, including (1) biosimilar price volatility with large quarter-on-quarter declines for most products; (2) perverse economic incentives that encourage providers to use more expensive reference products because reimbursement dynamics make them more profitable; (3) complex rebate structures that create barriers to biosimilar access; and (4) ongoing changes to the legal and regulatory environment, including evidence requirements to gain "interchangeable" status. We conclude with an overview of potential policy solutions to address the sustainability opportunities and threats. The authors welcome the opportunity to advance this dialogue toward action and encourage additional stakeholders to join the effort. We are optimistic that, through informed decision-making and compromise, we can collectively achieve a robust and sustainable US biosimilars market that appropriately benefits all stakeholders.
生物类似药在现代医学实践中发挥着关键作用,但由于其成本高昂,也给支付方、患者和其他利益相关者带来了挑战。生物类似药可以减轻参照生物疗法的成本压力,因为它们的定价通常至少低 25%,为提供尖端的生物疗法的同时管理护理成本提供了一种手段。事实上,美国医疗保健系统已经通过使用生物类似药节省了约 236 亿美元。然而,市场仍处于发展的初期阶段,如果不能建立可持续的市场条件,早期的成本节约成功并不能保证持续。为了更好地了解利益相关者对美国生物类似药市场可持续性的机遇和威胁的看法,2023 年 12 月召开了一次多方利益相关者圆桌讨论,与会者包括医疗保健支付方、提供者、自我保险雇主、制造商和生物类似药研究和倡导组织。本文作者是圆桌会议的参与者,旨在提出具体的机遇和威胁,供利益相关者考虑,以更好地促进美国生物类似药市场的可持续发展条件。我们强调了一些要点,包括:(1)大多数产品的季度价格波动较大,季度价格大幅下降;(2)由于报销动态使利润更高,导致提供者使用更昂贵的参照产品的不良经济激励;(3)复杂的回扣结构阻碍了生物类似药的获取;(4)法律和监管环境的持续变化,包括获得“可互换”地位的证据要求。最后,我们概述了潜在的政策解决方案,以解决可持续性的机遇和威胁。作者欢迎有机会将这一对话推进到行动,并鼓励更多的利益相关者加入这一努力。我们乐观地认为,通过明智的决策和妥协,我们可以共同实现一个强大和可持续的美国生物类似药市场,使所有利益相关者都能从中受益。