Verici Dx PLC Final results timing
April 24 2023 - 2:00AM
RNS Non-Regulatory
TIDMVRCI
Verici Dx PLC
24 April 2023
Verici Dx plc
("Verici Dx" or the "Company")
Final results timing
Verici Dx plc (AIM: VRCI), a developer of advanced clinical
diagnostics for organ transplant, announces that it expects to
report its final results for the year ended 31 December 2022 before
the end of May 2023.
Verici Dx remains on track to report the full data readout from
its Clarava(TM) validation trial during Q2 2023.
As indicated in the March progress update announcement, the
Company had a cash balance of $9.81m as at 31 December 2022, which
is expected to provide a cash runway until mid-2024.
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 wmanagement 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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END
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