New Therapies Laboratory, Health Research Institute-Fundación Jiménez Díaz University Hospital (IIS-FJD), Madrid, Spain.
Department of Surgery, Fundación Jiménez Díaz University Hospital, Madrid, Spain.
Expert Opin Biol Ther. 2023 Jul-Dec;23(12):1197-1202. doi: 10.1080/14712598.2023.2274911. Epub 2023 Dec 28.
This study provides an overview of the development of the first drug authorized for use in cell therapy.
We analyze the case of darvadstrocel, an example of a successful cell-therapy drug used worldwide to treat Crohn's perianal fistula. A bibliographic-historical analysis of the first cellular treatment approved by the EMA, including relevant aspects concerning the authors, who were involved in the whole process. We would like to highlight the following messages: Development: The article describes the development process of the drug, from initial concept through the clinical trial phases. Learning from failure: In describing the development of darvadstrocel, the authors highlight the importance of learning from failures, which is crucial to achieving successful outcomes. Collaboration: The article underscores the need for collaboration between public and private institutions to facilitate the advancement of cell-therapy drugs and ensure efficiency while adhering to regulatory guidelines.
Regulatory requirements play a crucial role in the design and development of advanced therapies such as cell-therapy drugs. The findings of this study underscore the significance of appropriate disease application, meticulous donor selection, robust manufacturing processes, and proper therapy administration. Only by adopting these measures can cell-therapy drugs successfully complete all phases of the clinical trial process.
本研究概述了第一种获准用于细胞治疗的药物的发展历程。
我们分析了达伐西特罗cel 的案例,这是一种在全球范围内成功用于治疗克罗恩病肛周瘘的细胞治疗药物的范例。对 EMA 批准的第一种细胞治疗药物进行了文献历史分析,包括与参与整个过程的作者相关的相关方面。我们想强调以下信息:
发展:本文描述了药物的开发过程,从最初的概念到临床试验阶段。
从失败中学习:在描述达伐西特罗 cel 的开发过程中,作者强调了从失败中学习的重要性,这对于取得成功的结果至关重要。
合作:本文强调了公共和私营机构之间合作的必要性,以促进细胞治疗药物的发展,并在遵守监管指南的同时确保效率。
监管要求在细胞治疗药物等先进疗法的设计和开发中起着至关重要的作用。本研究的结果强调了适当的疾病应用、精心的供体选择、稳健的制造工艺和适当的治疗管理的重要性。只有采取这些措施,细胞治疗药物才能成功完成临床试验的所有阶段。