Renalytix plc
("Renalytix" or the
"Company")
kidneyIntelX.dkd Published in Journal of the
American Society of Nephrology
LONDON and NEW
YORK, 6
February 2025 -
Renalytix plc (LSE: RENX) (OTCQB: RNLXY), which is
commercialising kidneyintelX.dkd, the only FDA-approved and Medicare reimbursed prognostic test to support
early-stage risk assessment for chronic kidney
disease, notes the publication of
the paper
kidneyintelX.dkd: An Innovation in Precision Medicine for Diabetic
Kidney Disease in
the Journal of the American Society of Nephrology (JASN), the
leading journal in the advancement of understanding and treatment
of kidney diseases.
The paper, published by invitation
for dissemination of innovative technologies, highlights
kidneyintelX.dkd as a critical risk
assessment tool to enable a personalised approach to treatment and
identification of those who would benefit most from multifaceted
therapy to slow the progression of DKD.
The publication also discusses the inclusion of
kidneyintelX.dkd in the
recently published KDIGO guidelines, which recommends "risk
assessment to assist with delivery of personalized care for people
with CKD":
"With
multiple new drug classes now available for DKD management in
addition to baseline RAAS inhibition, precision medicine solutions
such as kidneyintelX.dkd can change the current paradigm to a more
individualized approach. Some experts advocate an 'accelerated
risk-based approach' in which prioritization for 'quadruple
therapy' is reserved for those at highest absolute risk for
progression, given costs and potential adverse
events."
This is particularly relevant with
the recent regulatory approvals of Ozempic® for treatment of
DKD, further fuelling the need for an accelerated risk-based
approach targeting those at the highest risk of progression,
thereby ensuring the best possible health outcomes and avoiding
unnecessary, expensive treatments for those at lower
risk.
Fergus Fleming, Chief Technology Officer of Renalytix,
commented:
"The age of precision medicine in chronic disease is just
beginning and will be central to preventative care, improved
patient outcomes, and control of spiralling healthcare costs.
We welcome the publication of the kidneyintelX.dkd innovation in
this prestigious journal which will help to better inform the
nephrology and wider healthcare community on the power and utility
of biomarker -based early risk assessment with
kidneyintelX.dkd.
"With multiple new drugs coming into wider use in the clinic,
including Novo Nordisk's achievement this month securing approval
for Ozempic for the treatment of DKD, the ability to accurately
understand a patient's disease risk is paramount. We have invested
over six years developing kidneyintelX.dkd to deliver an accurate,
FDA regulated, Medicare reimbursed prognosis directly to physicians
charged with making timely therapeutic
decisions."
The full text of the publication
will be available here in due course: https://www.kidneyintelx.com/evidence/
For further information,
please contact:
Renalytix plc
|
www.renalytix.com
|
James McCullough, CEO
|
Via
Walbrook PR
|
|
|
Stifel (Nominated Adviser and Joint Broker)
|
Tel: 020
7710 7600
|
Nicholas Moore / Nick Harland / Ben
Good
|
|
|
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Oberon Capital
(Joint Broker)
|
Tel: 020
3179 5300
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Mike Seabrook / Nick Lovering
|
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Walbrook PR Limited
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Tel: 020
7933 8780 or renalytix@walbrookpr.com
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Paul McManus / Alice Woodings
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Mob: 07980 541 893 /
07407 804 654
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About
Renalytix (www.renalytix.com)
Renalytix (LSE: RENX) (OTCQB: RNLXY) is an
artificial intelligence-enabled in vitro diagnostics company, focused
on optimizing clinical management of kidney disease to drive
improved patient outcomes. Renalytix has received FDA approval and
Medicare reimbursement for kidneyintelX.dkd which is now offered
commercially in the United States.
Unrecognized and uncontrolled kidney disease
remains one of the largest barriers to controlling cost and
suffering in the United States and the United Kingdom's medical
system, affecting over 14 million and 8 million people,
respectively. After five years of development and clinical
validation, kidneyintelX.dkd is the only
FDA-approved and Medicare reimbursed prognostic tool capable of
understanding a patient's risk with kidney disease early where
treatment has maximal effect. kidneyintelX.dkd is now being deployed
across large physician group practices and health systems in select
regions of the United States.
The over 10,000 patients that have been tested
by kidneyintelX.dkd have
produced a substantial body of real-world performance data. In
patient populations where kidneyintelX.dkd has been deployed, a
demonstrated and significant increase in diagnosis, prognosis, and
treatment rates have been recorded. kidneyintelX.dkd now has full
reimbursement established by Medicare, the largest insurance payer
in the United States, at $950 per reportable result. kidneyintelX.dkd is also recommended
for use in the international chronic kidney disease clinical
guidelines (KDIGO).
Disclosure:
KidneyIntelX is based on innovative technology developed by Mount
Sinai faculty and licensed to Renalytix. Mount Sinai
faculty-inventors and Mount Sinai have equity ownership in
Renalytix.