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RCS - Verici Dx PLC - Product rebranding as Tutivia™

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RNS Number : 4499B  Verici Dx PLC  03 October 2022

RNS REACH

 

Verici Dx plc

("Verici Dx" or the "Company")

 

Product rebranding as Tutivia™

 

Verici Dx's post-transplant test, Tuteva, to be rebranded as Tutivia™

 

Verici Dx plc (AIM: VRCI), a developer of advanced clinical diagnostics for
organ transplant, announces that its post-transplant blood test focused on
acute rejection, has been rebranded as Tutivia™.

 

Tutivia™ (formerly known as Tuteva), is a blood-based RNA signature for a
risk score for acute rejection, and will be the first test commercialised on
the Verici transplant biomarker platform, with a soft commercial launch in the
United States expected later in 2022.

 

The first three products on the platform are:

·      Clarava™, a pre-transplant prognosis test for the risk of early
acute rejection;

·      Tutivia™, a post-transplant test focused upon acute rejection,
including sub-clinical rejection; and

·      Protega™, a post-transplant test that aims to predict the risk
of fibrosis and long-term graft failure

 

Enquiries:

 

 Verici Dx                                                www.v (http://www.vericidx.com) ericidx (http://www.vericidx.com) .com
                                                          (http://www.vericidx.com)
 Sara Barrington, CEO                                     Via Walbrook PR
 Julian Baines, Chairman

 Singer Capital Markets (Nominated Adviser & Broker)      Tel: 020 7496 3000
 Aubrey Powell / Kailey Aliyar / Sam Butcher

 Walbrook PR Limited                                      Tel: 020 7933 8780 or vericidx@walbrookpr.com
                                                          (mailto:renalytix@walbrookpr.com)
 Paul McManus / Sam Allen                                 Mob: 07980 541 893 / 07502 558 258

 

 

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About Verici Dx plc www.vericidx.com (http://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, including through 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.

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