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与罕见病相关产业建立互动关系:经验教训与持续挑战。

Developing interactions with industry in rare diseases: lessons learned and continuing challenges.

机构信息

Division of Genetics and Metabolism, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA.

Section of Genetics and Metabolism, Department of Pediatrics, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.

出版信息

Genet Med. 2020 Jan;22(1):219-226. doi: 10.1038/s41436-019-0616-9. Epub 2019 Jul 24.

Abstract

The National Institutes of Health (NIH) established the Rare Diseases Clinical Research Network to address the unique challenges of performing research on rare diseases. The Urea Cycle Disorders Consortium (UCDC) was one of the original ten consortia established. The UCDC represents a unique partnership among clinicians, patients, and the NIH with a primary goal of increasing the development of therapeutics that improve patient outcomes for persons affected with a UCD. Based in part on financial incentives associated with the Orphan Drug Act biopharmaceutical and investment entities have an intense interest in engaging with research consortia like the UCDC, which have compiled potentially valuable longitudinal data characterizing outcomes in a relatively large number of affected individuals. We describe the UCDC experience and the bases for evaluating partnerships with such private entities. We review early industry interactions, the development of policies and procedures, and describe the establishment of an Industry Relations Committee, including guiding principles. Challenges encountered, particularly in the transition when products are approved, and potential solutions are discussed. By building a framework for industry partnerships that guides us in resolving inevitable challenges, we can enthusiastically pursue novel and promising collaborations that can lead to breakthroughs in therapeutic interventions for patients.

摘要

美国国立卫生研究院 (NIH) 成立了罕见疾病临床研究网络,以应对开展罕见疾病研究的独特挑战。尿素循环障碍联盟 (UCDC) 是最初成立的十个联盟之一。UCDC 代表了临床医生、患者和 NIH 之间的独特合作关系,其主要目标是增加治疗方法的开发,以改善患有 UCD 的患者的治疗效果。部分基于孤儿药法案的财政激励措施,生物制药和投资实体对参与像 UCDC 这样的研究联盟有着浓厚的兴趣,UCDC 汇编了具有潜在价值的、描述大量受影响个体结局的纵向数据。我们描述了 UCDC 的经验以及评估与这类私营实体合作的基础。我们回顾了早期的行业互动、政策和程序的制定,并描述了行业关系委员会的建立,包括指导原则。讨论了所遇到的挑战,特别是在产品获得批准时的过渡阶段,以及潜在的解决方案。通过为行业合作建立一个指导我们解决不可避免挑战的框架,我们可以热情地追求新颖且有前途的合作,这可能会为患者的治疗干预带来突破。

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