Verici Dx plc
("Verici Dx" or the "Company")
Notice of Results
Verici Dx plc (AIM: VRCI), a developer of advanced clinical diagnostics for organ transplant, announces that it will report its final results for the year ended 31 December 2022 on Monday 5 June 2023.
The data read-out from the extended Clarava™ trial remains on track to be announced by the end of June, in line with previous guidance. An investor briefing covering the FY22 financial results together with an update on the Company's products will be scheduled at this stage.
Enquiries:
| Verici Dx | |
| Sara Barrington, CEO | Via Walbrook PR |
| Julian Baines, Chairman |
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| Singer Capital Markets (Nominated Adviser & Broker) | Tel: +44 20 7496 3000 |
| Aubrey Powell / Sam Butcher | |
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| Walbrook PR Limited | Tel: +44 20 7933 8780 or vericidx@walbrookpr.com |
| Paul McManus / Stephanie Cuthbert / Sam Allen | Mob: +44 7980 541 893 / +44 7796 794 663 / 07502 558 258 |
About Verici Dx plc www.vericidx.com
Verici Dx is a developer of a complementary suite of leading-edge tests forming a kidney transplant platform for personalised patient and organ response risk to assist clinicians in medical management for improved patient outcomes. The underlying technology is based upon artificial intelligence assisted transcriptomic analysis to provide RNA signatures focused upon the immune response and other biological pathway signals critical for transplant prognosis of risk of injury, rejection and graft failure from pre-transplant to late stage. The Company also has a mission to accelerate the pace of innovation by research using the fully characterised data from the underlying technology and collaboration with medical device, biopharmaceutical and data science partners.
The foundational research was driven by a deep understanding of cell-mediated immunity and is enabled by access to expertly curated collaborative studies in highly informative cohorts in kidney transplant.
Verici Dx's two lead products are Clarava™, a pre-transplant prognosis test for the risk of early acute rejection, and Tutivia™, a post-transplant test focused upon acute cellular rejection, including sub-clinical rejection. These products seek to measure how a patient is likely to respond, and is responding, to a kidney transplant. These products are underpinned by extensive patented and published scientific research from the leading Mount Sinai Medical Center, for which the Company holds an exclusive worldwide licence.
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