The Development and Validation of Technology for Time Critical Genomic Testing (DEVOTE) grant will provide the Company with acute care patient access and supporting infrastructure to assess the real world clinical performance of time-critical clinical tests in NHS settings. The Company confirms it expects to benefit from funding of approximately £1.2m, through the programme’s lead partner, the University of Manchester (“UoM”) that will support the evaluation, validation and implementation of the new Genedrive® CYP2C19 ID Kit. DEVOTE is funded through the Innovate grant, in-kind contributions, and other aligned funding, the vast majority of this funding will be paid directly to the UoM to support the Company’s initiatives.
The draft guidance from the UK’s National Institute for Health and Care Excellence (“NICE”) Diagnostics Assessment Programme “Clopidogrel genotype testing after ischaemic stroke or transient ischaemic attack” has recommended that CYP2C19 genotyping should be used before clopidogrel administration in the management of ischemic stroke patients. NICE’s final report is now due in December 2023, and the Company is working to provide final performance specifications for the report. The work for DEVOTE will mostly contribute towards the extended clinical performance data now required for IVDR registration of new products in the EU.
James Cheek, Chief Executive Officer of genedrive plc, said: “The DEVOTE programme is an incredible opportunity for us to partner once again with the University of Manchester in developing time-critical genetic test solutions. The grant funding allows us to avoid costs that would otherwise have been incurred by genedrive directly and to benefit from accessing the Acute Medicine Unit, which is paramount to our product validation under IVDR.”
