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The Development and Validation of Technology for Time Critical Genomic Testing (DEVOTE) Programme

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A bedside genetic test could tell a stroke doctor within minutes which patients need a different, more expensive blood thinner—but only if the technology can be made fast enough for real-time prescribing. Current genetic tests take weeks or months to return results, making them useless for guiding time-sensitive decisions such as which drug to give a patient arriving at hospital with a stroke. This programme brings together biotechnology companies, universities, and clinicians to build a practical pipeline for turning genetic biomarkers into rapid, bedside tests. Three exemplar projects will demonstrate the approach: a stroke-treatment test, an ultra-rapid test to guide antibiotic choice, and a comprehensive pharmacogenetic panel with software that delivers results to clinicians at the point of need. If successful, the programme will remove a major bottleneck in genomic medicine—the gap between discovering a useful genetic marker and using it in routine care. Faster prescribing could reduce adverse drug reactions, improve treatment outcomes, and lower healthcare costs. The programme also aims to create commercial assets and attract further investment into Greater Manchester’s diagnostics sector, with the goal of sustaining innovation in time-critical genomic testing over the next decade.

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A biomarker is a chemical or signal which can be measured from the human body to help to diagnose disease or predict future health states. Biomarkers are commonly used in healthcare to guide patient management, but there is a major translational bottleneck between the discovery of a clinically relevant biomarker and its implementation in routine practice to help patients. This is particularly true of genetic biomarkers, defined as changes in our genetic code which predispose to disease or predict treatment outcomes. Many of these are related to _pharmacogenetics_, the concept that changes in our genetic code influence our response to medicines. At present, genetic tests are too slow to guide prescribing in day-to-day practice. Traditional genetic tests take many weeks or months to come back, which is far too slow to be used in most clinical settings. However, new technologies have the potential to change this. The challenge for biotechnology companies is understanding how best to implement these technologies in a given clinical setting. This project will address this by developing a translational pipeline with collaboration between industry, Universities, and healthcare professionals to support the development and implementation of time critical genomic testing technologies (The DEVOTE Programme). This builds on Greater Manchester's world leading reputation in this space, empowering industry to focus on their core business of technology development, whilst academic and clinical partners work to ensure said technologies are cost effective, well placed in the market, and designed with patients in mind. DEVOTE will demonstrate its value through three exemplar projects. * Development of a rapid genetic bedside test to guide treatment for patients after stroke (Genedrive plc & EMQN). * Using new and emerging biomaterials to develop an ultra-rapid genetic test, capable of detecting genetic changes to guide antibiotic therapy (Chromition Ltd and Epinal). * Creation of a comprehensive pharmacogenetic testing panel with an informatic solution to ensure results are available to clinicians at the point of need (APIS Assay Technologies Ltd & EMQN). These varied projects will show the flexibility of the DEVOTE programme and the outputs will not only improve the health of the population, but will create valuable industrial assets, resulting in further investment across Greater Manchester. The DEVOTE programme will continue to engage with other industrial partners beyond the lifecycle of this award, with a view to drive innovation and the translation of technologies over the next decade.

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