Strategic discussion on funding and access to therapies targeting rare diseases in Spain: an expert consensus paper

Author:

Zozaya N.ORCID,Villaseca J.,Abdalla F.,Ancochea A.,Málaga I.,Trapero-Bertran M.,Martín-Sobrino N.,Delgado O.,Ferré P.,Hidalgo-Vega A.

Abstract

Abstract Background In recent years, significant advances have been made in the field of rare diseases (RDs). However, there is a large number of RDs without specific treatment and half of these treatments have public funding in Spain. The aim of the FINEERR project was to carry out a multidisciplinary strategic discussion on the challenge of funding and access to RD-targeted drugs in Spain, in order to agree on specific proposals for medium-term improvement and hence support decision-making in the Spanish National Healthcare System (SNHS). Results The FINEERR Project was organized around a CORE Advisory Committee, which provided an overview, agreed on the design and scope of the project, and selected the members within each of four working groups (WG). Overall, 40 experts discussed and reached a consensus on different relevant aspects, such as conditioning factors for initial funding and access, evaluation and access to RD-targeted therapies, funding of these therapies, and implementation of a new funding and access model. From these meetings, 50 proposals were defined and classified by their level of relevance according to the experts. A descriptive analysis of responses was performed for each proposal. Thereafter, experts completed another questionnaire where they ranked the 25 most relevant proposals according to their level of feasibility of being implemented in the SNHS. The most relevant and feasible proposals were to improve: process of referral of patients with RDs, control over monitoring mechanisms, and communication between healthcare professionals and patients. Conclusions The FINEERR project may provide a starting point for stakeholders involved in the process of funding and access to RD-targeted therapies in Spain to provide the necessary resources and implement measures to improve both the quality of life and life expectancy of patients with RDs.

Funder

Roche España

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Reference41 articles.

1. Tumiene B, Kristoffersson U, Hedley V, Kääriäinen H. Rare diseases: past achievements and future prospects. J Community Genet. 2021;12(2):205–6.

2. Groft SC, Posada M, Taruscio D. Progress, challenges and global approaches to rare diseases. Acta Paediatr. 2021;110(10):2711–6.

3. Chan AYL, Chan VKY, Olsson S, Fan M, Jit M, Gong M, et al. Orphan drugs—access and unmet needs in 194 countries and six regions: a comprehensive policy review with content analysis. The Lancet. 2019;1(394):S72.

4. Comisión Europea. Evaluación conjunta del Reglamento (CE) no 1901/2006 del Parlamento Europeo y del Consejo, de 12 de diciembre de 2006, sobre medicamentos para uso pediátrico, y del Reglamento (CE) no 141/2000 del Parlamento Europeo y del Consejo, de 16 de diciembre de 1999, sobre medicamentos huérfanos. 2020. https://ec.europa.eu/health/sites/health/files/files/paediatrics/docs/orphan-regulation_eval_swd_2020-163_part-1.pdf. Accessed 22 Jun 2022.

5. OCDE. Pharmaceutical reimbursement and pricing in Germany. 2018. https://www.oecd.org/els/health-systems/Pharmaceutical-Reimbursement-and-Pricing-in-Germany.pdf. Accessed 19 May 2022.

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3