Your browser doesn't support javascript.
loading
Stakeholder perspectives on the sustainability of the United States biosimilars market.
Sullivan, Sean D; Humphreys, Sophia Z; Fox, David; Lockhart, Catherine M; Tait-Dinger, Ashley; Betancourt, Juan Diego; Komorny, Kenneth M; Haumschild, Ryan; Chester, Barry; Harman, Matthew; Roth, Joshua A.
Afiliação
  • Sullivan SD; CHOICE Institute, School of Pharmacy, University of Washington, Seattle.
  • Humphreys SZ; Curta, Inc., Seattle, WA.
  • Fox D; Sutter Health, Sacramento, CA.
  • Lockhart CM; Independent Consultant, Daytona Beach, FL.
  • Tait-Dinger A; Biologics and Biosimilars Collective Intelligence Consortium, Alexandria, VA.
  • Betancourt JD; Florida Alliance for Healthcare Value, Winter Springs.
  • Komorny KM; Pfizer, Inc., New York, NY.
  • Haumschild R; Moffitt Cancer Center, Tampa, FL.
  • Chester B; Emory Healthcare and Winship Cancer Institute, Atlanta, GA.
  • Harman M; Pfizer, Inc., New York, NY.
  • Roth JA; Employers Health, Canton, OH.
J Manag Care Spec Pharm ; : 1-8, 2024 Jul 16.
Article em En | MEDLINE | ID: mdl-39012302
ABSTRACT
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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article