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Published on: February 28, 2014
Levelling the playing field through the London Network of the UK clinical trials accelerator platform
Jessie Matthews1, Rebecca Dobra1, Gemma Wilson1
1Royal Brompton Hospital, Part of Guy's & St Thomas' Trust, London, UK.
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.
Insights
The UK Cystic Fibrosis Trust's Clinical Trials Accelerator Platform (CTAP) improved access to clinical trials for cystic fibrosis (CF) patients across London. This national initiative enhanced trial availability and participation by fostering collaboration among CF centers.
Area of Science:
- Medical Research
- Clinical Trials
- Genetics
Background:
- Cystic fibrosis (CF) is a severe genetic disorder impacting multiple organ systems and reducing life expectancy.
- Despite therapeutic advancements, a cure for CF remains elusive, necessitating ongoing clinical research.
- Numerous novel therapies are in development, with many clinical trials underway globally.
Purpose of the Study:
- To evaluate the effectiveness of the UK Cystic Fibrosis Trust's Clinical Trials Accelerator Platform (CTAP) in improving trial access for CF patients.
- To assess the collaborative efforts of London-based CF centers within the CTAP network.
- To identify strengths and areas for improvement in clinical trial delivery for chronic diseases.
Main Methods:
- Formation of a sub-network of four large and two smaller specialist CF centers in London.
- Implementation of a consortium-style collaboration to ensure equitable trial access and knowledge sharing.
- Review of practices through working group meetings and an online survey after four years of operation.
Main Results:
- The CTAP initiative successfully brought together 25 UK CF centers to enhance patient participation in clinical trials.
- The London sub-network facilitated broader trial portfolios and increased study options for UK patients.
- The review identified key strengths and areas for improvement in the CTAP program's operational practices.
Conclusions:
- The CTAP model demonstrates a successful national strategy for increasing access to CF clinical trials.
- Collaborative networks of specialist centers can improve research delivery and patient equity in chronic disease management.
- The findings offer valuable insights for other regions and chronic diseases aiming to enhance clinical trial participation.
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