Associate Professor, School of Public Policy and Administration, Carleton University, Ottawa, ON.
Healthc Policy. 2024 Aug;19(4):27-31. doi: 10.12927/hcpol.2024.27353.
Lexchin and Sirrs (2024) proposed five relevant principles to guide the use of federal funding for expensive drugs for rare diseases, including funding of outcomes-based risk-sharing agreements (OBRSAs) and proactive commitment and participation in the generation of high-quality evidence in a transparent way. This rejoinder, however, questions whether the federal funding should be used only to buy new drugs or whether it could be used to develop new drugs as well. It also examines what OBRSAs would require in terms of institutional capacities to allow the collection of real-world evidence.
莱克欣和赛尔斯(2024 年)提出了五项相关原则,以指导联邦资金用于治疗罕见病的昂贵药物,包括为基于结果的风险分担协议(OBRSAs)提供资金,以及以透明的方式积极承诺并参与高质量证据的生成。然而,这篇反驳文章质疑联邦资金是否应该仅用于购买新药,或者是否可以用于开发新药。它还研究了 OBRSAs 需要什么样的机构能力来允许收集真实世界的证据。