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在欧洲资助跨国研究者发起的临床研究:为什么以及如何?

Funding multinational investigator-initiated clinical studies in Europe: why and how?

机构信息

European Clinical Research Infrastructure Network (ECRIN), Paris, France.

Instituto de Salud Carlos III (ISCIII), Madrid, Spain.

出版信息

Trials. 2024 Oct 17;25(1):689. doi: 10.1186/s13063-024-08548-1.

Abstract

Investigator-initiated clinical studies (IICSs), also referred to as non-commercial, academic or independent clinical studies, address important research questions that are usually neglected by industry despite their high societal value. Indeed, industry may direct their focus and resources on studies that will yield results and products that can ultimately generate revenue for the company. Conversely, IICS research questions include (a) refining or getting new indications of available treatments (drug repurposing); (b) optimisation, by comparing various health products or treatment regimens; and (c) innovation, especially for advanced therapies. Multinational IICSs increase the scientific quality of the data by exchange of research ideas, scientific techniques and tools. Participation of patients from different geographical, social and ethnic backgrounds equally adds to the value of study results and yields more generalisable evidence than a study confined to a single geographical location. Multinational IICSs are generally sponsored by non-profit/academic organisations and publicly funded. Funding has been already identified as a main challenge for the conduct IICS and especially for clinical trials (IICTs, IICS where a medical intervention is directly tested). Main barriers to the conduct of multinational IICTs with public funding include: Limitations of budget and duration of the eligibility of costs Lack of flexibility to move funds transnationally Tendering rules Complexity in the reporting of the eligible costs to funders We describe why there is a need to support multinational IICS, what should be their objectives and what are the current funding mechanisms in Europe. Strategies for funding multinational IICS should evolve to mitigate identified barriers, thus facilitating research that can provide answers to highly relevant questions in healthcare which are less likely to be answered by studies funded by the pharmaceutical and medical device industry.

摘要

研究者发起的临床研究(IICS),也称为非商业性、学术性或独立性临床研究,旨在解决重要的研究问题,而这些问题通常会被行业忽视,尽管它们具有很高的社会价值。实际上,行业可能会将其关注和资源集中在那些能够产生结果和产品的研究上,这些产品最终可以为公司带来收入。相反,IICS 研究问题包括(a)完善或获得现有治疗方法的新适应症(药物再利用);(b)通过比较各种健康产品或治疗方案进行优化;(c)创新,特别是对于先进疗法。跨国 IICS 通过交流研究思路、科学技术和工具来提高数据的科学质量。来自不同地理、社会和种族背景的患者参与同样增加了研究结果的价值,并产生比仅限于单一地理位置的研究更具普遍性的证据。跨国 IICS 通常由非营利/学术组织和公共资金赞助。资金已被确定为进行 IICS 特别是临床研究(IICTs,直接测试医学干预的 IICS)的主要挑战。有公共资金支持的跨国 IICT 进行的主要障碍包括:

  • 成本资格的预算和期限限制

  • 缺乏跨国资金转移的灵活性

  • 招标规则

  • 向资助者报告合格成本的复杂性

我们描述了为什么需要支持跨国 IICS,它们的目标应该是什么,以及欧洲目前的资金机制是什么。资助跨国 IICS 的策略应该发展,以减轻已确定的障碍,从而促进研究,为医疗保健中高度相关的问题提供答案,而这些问题不太可能通过制药和医疗器械行业资助的研究来回答。

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