Levelling the playing field through the London Network of the UK clinical trials accelerator platform

IF 1.4 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Contemporary Clinical Trials Communications Pub Date : 2024-04-26 DOI:10.1016/j.conctc.2024.101301
Jessie Matthews , Rebecca Dobra , Gemma Wilson , Lucy Allen , Cara Bossley , Rebecca Brendell , Rossa Brugha , Danielle Brown , Sarah Brown , Shenna Cadiente , Loren Cameron , Gwyneth Davies , Charlotte Dawson , Stuart Elborn , Dominic Hughes , Jess Longmate , Patricia Macedo , Leonidas Pappas , Caroline Pao , Chris Round , Jane C. Davies
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Abstract

Cystic fibrosis (CF) is a multisystem, genetic disease with a significantly reduced life expectancy. Despite substantial progress in therapies in the last 10–15 years, there is still no cure. There are dozens of drugs in the development pipeline and multiple clinical trials are being conducted across the globe. The UK Cystic Fibrosis Trust's (CFT) Clinical Trials Accelerator Platform (CTAP) is a national initiative bringing together 25 UK based CF centres to support the CF community in accessing and participating in CF clinical trials. CTAP enables more CF centres to run a broader portfolio of trials and increases the range of CF studies available for UK patients.

There are four large specialist CF centres based in London, all within a small geographical region as well as two smaller centres which deliver CF care. At the launch of CTAP, these centres formed a sub-network in a consortium-style collaboration. The purpose of the network was to ensure equity of access to trials for patients across the UK's capital, and to share experience and knowledge. Four years into the programme we have reviewed our practices through working group meetings and an online survey. We sought to identify strengths and areas for improvement. We share our findings here, as we believe they are relevant to others delivering research in regions outside of London and in other chronic diseases.

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通过英国临床试验加速器平台的伦敦网络创造公平竞争环境
囊性纤维化(CF)是一种多系统遗传疾病,患者的预期寿命会明显缩短。尽管在过去的 10-15 年里,治疗方法取得了长足进步,但仍无法治愈。目前有数十种药物正在研发过程中,全球各地正在进行多项临床试验。英国囊性纤维化信托基金(CFT)的临床试验加速平台(CTAP)是一项全国性倡议,它将英国的 25 家 CF 中心聚集在一起,为 CF 社区获取和参与 CF 临床试验提供支持。CTAP 使更多的 CF 中心能够开展更广泛的试验组合,并扩大了英国患者可获得的 CF 研究范围。在启动 CTAP 时,这些中心组成了一个联盟式合作的子网络。该网络的目的是确保英国首都的患者能够公平地获得试验机会,并分享经验和知识。该计划实施四年来,我们通过工作组会议和在线调查对我们的做法进行了回顾。我们试图找出优势和需要改进的地方。我们在此分享我们的发现,因为我们相信这些发现对其他在伦敦以外地区开展研究和其他慢性疾病研究的机构也有借鉴意义。
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来源期刊
Contemporary Clinical Trials Communications
Contemporary Clinical Trials Communications Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
2.70
自引率
6.70%
发文量
146
审稿时长
20 weeks
期刊介绍: Contemporary Clinical Trials Communications is an international peer reviewed open access journal that publishes articles pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from a wide range of disciplines including medicine, life science, pharmaceutical science, biostatistics, epidemiology, computer science, management science, behavioral science, and bioethics. Contemporary Clinical Trials Communications is unique in that it is outside the confines of disease specifications, and it strives to increase the transparency of medical research and reduce publication bias by publishing scientifically valid original research findings irrespective of their perceived importance, significance or impact. Both randomized and non-randomized trials are within the scope of the Journal. Some common topics include trial design rationale and methods, operational methodologies and challenges, and positive and negative trial results. In addition to original research, the Journal also welcomes other types of communications including, but are not limited to, methodology reviews, perspectives and discussions. Through timely dissemination of advances in clinical trials, the goal of Contemporary Clinical Trials Communications is to serve as a platform to enhance the communication and collaboration within the global clinical trials community that ultimately advances this field of research for the benefit of patients.
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