Renalytix plc (NASDAQ: RNLX) (LSE: RENX) today announced the
execution of a Co-operative Research and Development Agreement
(CRADA) with the U.S. Veterans Health Administration Innovation
Ecosystem (VHA IE) to install the KidneyIntelX solution inside the
VA Health System’s Cloud Infrastructure and interface it with the
VA Electronic Health Record Systems. This marks a significant
milestone in enabling providers at 171 VA Medical Centers (VAMCs)
and related outpatient clinics to order and receive test results in
a seamless manner.
The outputs from this agreement will be instrumental in ensuring
that Veterans and their providers have the same access to the
benefits of early-stage risk assessment of patients with diabetic
kidney disease (DKD) by KidneyIntelX and the improvements in care
and outcomes that have been demonstrated in published studies in
other health systems1. By installing the KidneyIntelX platform
inside the VA infrastructure through this innovative approach, one
of the first such implementations by the VA, the stringent
requirements for the security of Veteran’s health information and
data will be assured.
The KidneyIntelX solution will complement the Department of
Veterans Affairs (VA) / Department of Defense (DoD) into the
clinical practice guideline for the management of CKD (Version
4.0-2019 Care Directive 1053) entitled, Chronic Kidney Disease
Prevention, Early Recognition and Management2. According to the
March 17, 2020, Veterans Health Administration (VHA) Directive
1053, approximately 960,000 Veterans, or 11%, meet the established
criteria for chronic kidney disease (CKD). However, less than half
of those Veterans, 320,000, or 5%, have been formally diagnosed
with CKD. The annual VHA cost related to CKD is estimated to be $19
billion dollars. Given that 65% of the Veterans who may have CKD
may be improperly or not diagnosed and treated, this collaboration
represents a significant opportunity for the VHA to immediately
initiate a broader CKD assessment for chronic disease population
health management.
Integration with multiple systems such as the VA Computerized
Patient Record System (CPRS), Cerner, and Veterans Information
Systems and Technology Architecture (VistA) will streamline
operations to overcome adoption hurdles and enable access to
KidneyIntelX for a large, at-risk patient population.
The program will commence immediately and will be implemented on
a phased basis over an approximate 18-month period.
According to Fergus Fleming, Chief Technology Officer of
Renalytix, “The opportunity to work collaboratively with the VHA
Innovation Ecosystem and Office of Information Technology (OIT) at
a national level to integrate KidneyIntelX within the VA cloud is
transformational, and reaching this milestone significantly
advances our shared value proposition for this collaboration, to
introduce an innovative approach for early risk assessment of CKD
into care for this important population.”
Renalytix became an authorized laboratory service provider for
all government health locations under the General Services
Administration (GSA) contract announced in April, 2021.
_______________1 Tokita J, Vega A, et al. Real World Evidence
and Clinical Utility of KidneyIntelX on Patients With Early-Stage
Diabetic Kidney Disease: Interim Results on Decision Impact and
Outcomes. J Prim Care Community Health. 2022 Jan-Dec;
13:21501319221138196.2 VHA 2019 Care Directive 1053: Chronic Kidney
Disease Prevention, Early Recognition and Management.
About Kidney Disease
Kidney disease is a public health epidemic affecting over 850
million people globally.1 The Centers for Disease Control and
Prevention estimates that 15% of U.S. adults, or over 37 million
people2, have chronic kidney disease (CKD). Nearly 95% of people
with CKD are in early stages 1-33. Despite its magnitude,
early-stage (1-3) CKD is underdiagnosed and undertreated, largely
because it’s asymptomatic at this time in the disease. As many as 9
in 10 adults with CKD, and 2 in 5 adults with severe CKD do not
know they have the condition.3
About Renalytix
Renalytix (NASDAQ: RNLX) (LSE: RENX) is an in-vitro diagnostics
and laboratory services company that is the global founder and
leader in the new field of bioprognosis™ for kidney health.
The leadership team, with a combined 200+ years of healthcare and
in-vitro diagnostic experience, has designed its KidneyIntelX
laboratory developed test to enable risk assessment for rapid
progressive decline in kidney function in adult patients with T2D
and early CKD (stages 1-3). We believe that by understanding how
disease will progress, patients and providers can take action early
to improve outcomes and reduce overall health system costs. For
more information, visit www.renalytix.com.
About KidneyIntelX™
KidneyIntelX™ is a laboratory developed test demonstrated
to be a reliable, bioprognostic™ methodology that yields a
simple-to-understand, custom risk score, enabling prediction of
which adult patients with T2D and early CKD (stages 1-3) are at
low, intermediate or high risk for rapid progressive decline in
kidney function. By combining information from KidneyIntelX with
newer cardio- and reno-protective therapies, doctors will have more
information in determining which patients are at higher versus
lower risk for rapid disease progression and may be able to more
appropriately target resources and guideline-recommended treatments
to advance kidney health. KidneyIntelX is supported by a growing
body of clinical, utility and health economic studies (including a
validation study of two large cohorts) and has a demonstrated a 72%
improvement in predicting those patients who are at high risk for
rapid progressive decline in kidney function versus the current
standard of care (eGFR and UACR). KidneyIntelX has received
Breakthrough Device Designation from the U.S. Food and Drug
Administration and Renalytix has submitted for De Novo marketing
authorization. To learn more about KidneyIntelX and review the
evidence, visit www.kidneyintelx.com.
Sources
1 https://www.theisn.org/blog/2020/11/27/more-than-850-million-worldwide-have-some-form-of-kidney-disease-help-raise-awareness/2 https://www.cdc.gov/kidneydisease/publications-resources/ckd-national-facts.html3 https://www.cdc.gov/kidneydisease/basics.html
Forward Looking Statements
Statements contained in this press release regarding matters
that are not historical facts are “forward-looking statements”
within the meaning of the Private Securities Litigation Reform Act
of 1995, as amended. Examples of these forward-looking statements
include statements concerning: the potential benefits, including
economic savings, of KidneyIntelX, the future impact of
KidneyIntelX on clinical decision-making and outcomes, the
potential for KidneyIntelX to receive regulatory approval from the
FDA, the commercial prospects of KidneyIntelX, if approved,
including whether and to what extent KidneyIntelX will be
successfully adopted by physicians and distributed and marketed,
our expectations regarding reimbursement decisions and the ability
of KidneyIntelX to curtail costs of chronic and end-stage kidney
disease, optimize care delivery, address systemic inequalities and
improve patient outcomes. The results presented in this press
release are interim results; subsequent interim results and full
results may vary and may not be consistent with these interim
results. Words such as “anticipates,” “believes,” “estimates,”
“expects,” “intends,” “plans,” “seeks,” and similar expressions are
intended to identify forward-looking statements. We may not
actually achieve the plans and objectives disclosed in the
forward-looking statements, and you should not place undue reliance
on our forward-looking statements. Any forward-looking statements
are based on management’s current views and assumptions and involve
risks and uncertainties that could cause actual results,
performance, or events to differ materially from those expressed or
implied in such statements. These risks and uncertainties include,
among others: that KidneyIntelX is based on novel artificial
intelligence technologies that are rapidly evolving and potential
acceptance, utility and clinical practice remains uncertain; we
have only recently commercially launched KidneyIntelX; and risks
relating to the impact on our business of the COVID-19 pandemic or
similar public health crises. These and other risks are described
more fully in our filings with the Securities and Exchange
Commission (SEC), including the “Risk Factors” section of our
annual report on Form 20-F filed with the SEC on October 31, 2022,
and other filings we make with the SEC from time to time. All
information in this press release is as of the date of the release,
and we undertake no obligation to publicly update any
forward-looking statement, whether as a result of new information,
future events, or otherwise, except as required by law.
Media Contacts:United
States:RenalytixKarla
Gonyekgonye@renalytix.com617-590-5731media@renalytix.com
Outside of the United States:Walbrook
PR LimitedPaul McManus / Alice Woodings
Tel: 020 7933 8780 or renalytix@walbrookpr.comMob: 07980
541 893 / 07407 804 654
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