CTI Clinical Trial and Consulting Services, Lisboa, Portugal.
Eur J Health Econ. 2022 Mar;23(2):155-163. doi: 10.1007/s10198-021-01276-2. Epub 2021 Jun 9.
The emergence of advanced therapy medicinal products (ATMPs), a disruptive class of health technologies, is generating important challenges in terms of value assessment and their high prices introduce critical access and affordability concerns. The aim of this article is to analyze the challenges of traditional value assessment and price and reimbursement methods in the evaluation of ATMPs and to characterize the current and prospective financing solutions that may ensure patient access and affordability for these health technologies. Standard Health Technology Assessment (HTA) is not designed for ATMPs, and may delay access to these health technologies, thus a broader concept of value is required. As a consequence, value-based pricing methodologies have been gaining terrain to cope with the specific challenges of ATMPs. The pricing and reimbursement framework should ensure the balance between encouragements to innovation and maximization of value for money for payers, through the attribution of a fair price to new health technologies. Early scientific advice by regulatory and HTA bodies to developers is key, as it will contribute to diminish the perspective gap between developers, regulators and payers. The high efficacy/high price dynamic of many advanced therapies will demand novel financing models, both in the EU and US. Managed entry agreements (MEA), with financing being conditional to the submission of additional evidence, associated with methods of leased payments, may offer effective strategies to address the uncertainties caused by the evidence gap associated with ATMPs, ensuring affordable and sustained access.
先进治疗药物产品(ATMPs)的出现是一类具有颠覆性的医疗技术,在价值评估方面带来了重要挑战,其高昂的价格引发了关键的可及性和负担能力问题。本文旨在分析传统的价值评估以及 ATMP 定价和报销方法所面临的挑战,并描述当前和未来可能确保这些医疗技术可及性和负担能力的融资解决方案。标准的卫生技术评估(HTA)并不适用于 ATMPs,可能会延迟这些医疗技术的应用,因此需要更广泛的价值概念。因此,基于价值的定价方法已经逐渐得到应用,以应对 ATMPs 的特殊挑战。定价和报销框架应通过为新的医疗技术赋予公平的价格,在鼓励创新和为支付方实现最大价值之间取得平衡。监管机构和 HTA 机构向开发者提供早期的科学建议至关重要,因为这有助于缩小开发者、监管机构和支付方之间的观点差距。许多先进疗法的高疗效/高价格动态将需要在欧盟和美国都采用新的融资模式。管理准入协议(MEA),即融资取决于提交额外证据,同时伴随租赁付款方式,可能为解决与 ATMPs 相关的证据差距所带来的不确定性提供有效的策略,确保负担得起和可持续的可及性。