Verici Dx PLC Notice of Results (0916B)
31 Mai 2023 - 8:00AM
UK Regulatory
TIDMVRCI
RNS Number : 0916B
Verici Dx PLC
31 May 2023
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 (TM) 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 www.v ericidx .com
Sara Barrington, CEO Via Walbrook PR
Julian Baines, Chairman
Singer Capital Markets (Nominated Tel: +44 20 7496 3000
Adviser & Broker)
Aubrey Powell / Sam Butcher
Walbrook PR Limited Tel: +44 20 7933 8780 or vericidx@walbrookpr.com
Paul McManus / Stephanie Cuthbert Mob: +44 7980 541 893 / +44 7796
/ 794 663 /
Sam Allen 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(TM), a pre-transplant
prognosis test for the risk of early acute rejection, and
Tutivia(TM), 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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