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从罕见病药物扩大使用中获取证据:挑战与建议

Generating Evidence from Expanded Access Use of Rare Disease Medicines: Challenges and Recommendations.

作者信息

Polak Tobias B, Cucchi David G J, van Rosmalen Joost, Uyl-de Groot Carin A, Darrow Jonathan J

机构信息

Erasmus School of Health Policy and Management, Erasmus University Rotterdam, Rotterdam, Netherlands.

Department of Biostatistics, Erasmus University Rotterdam, Rotterdam, Netherlands.

出版信息

Front Pharmacol. 2022 May 23;13:913567. doi: 10.3389/fphar.2022.913567. eCollection 2022.

Abstract

Patients with rare diseases often have limited or no options for approved treatments or participation in clinical trials. In such cases, expanded access (or "compassionate use") provides a potential means of accessing unapproved investigational medicines. It is also possible to capture and analyze clinical data from such use, but doing so is controversial. In this perspective, we offer examples of evidence derived from expanded access programs for rare diseases to illustrate its potential value to the decision-making of regulators and payers in the European Union and the United States. We discuss ethical and regulatory aspects to the use of expanded access data, with a focus on rare disease medicines. The heterogeneous approach to expanded access among countries within the European Union leaves uncertainties to what extent data can be collected and analyzed. We recommend the issuance of new guidance on data collection during expanded access, harmonization of European pathways, and an update of existing European compassionate use guidance. We hereby aim to clarify the supportive role of expanded access in evidence generation. Harmonization across Europe of expanded access regulations could reduce manufacturer burdens, improve patient access, and yield better data. These changes would better balance the need to generate quality evidence with the desire for pre-approval access to investigational medicine.

摘要

罕见病患者通常在获批治疗或参与临床试验方面选择有限或没有选择。在这种情况下,扩大使用(或“同情用药”)提供了一种获取未获批研究性药物的潜在途径。从这种使用中收集和分析临床数据也是可能的,但这样做存在争议。从这个角度出发,我们提供了罕见病扩大使用项目的证据示例,以说明其对欧盟和美国监管机构及支付方决策的潜在价值。我们讨论了使用扩大使用数据的伦理和监管方面,重点是罕见病药物。欧盟国家之间在扩大使用方面的异质做法使得在何种程度上能够收集和分析数据存在不确定性。我们建议发布关于扩大使用期间数据收集的新指南,协调欧洲的途径,并更新现有的欧洲同情用药指南。我们在此旨在阐明扩大使用在证据生成中的支持作用。欧洲扩大使用法规的协调可以减轻制造商负担,改善患者获取药物的机会,并产生更好的数据。这些变化将更好地平衡生成高质量证据的需求与在研究性药物获批前获取药物的愿望。

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