("Nanox" or the "Company," Nasdaq: NNOX), an innovative medical
imaging technology company, today announced that its deep-learning
medical imaging analytics subsidiary, Nanox AI Ltd., received
510(k) clearance by the U.S. Food and Drug Administration (FDA) for
HealthFLD, an artificial intelligence (AI) software that provides
automated qualitative and quantitative analysis of liver
attenuation from routine contrast and non-contrast chest and
abdomen CT scans in patients between the ages of 18 to 75.
HealthFLD is intended to support clinicians in the detection of
fatty liver, correlated with hepatic steatosis, an early sign of
metabolic dysfunction-associated steatotic liver disease (MASLD),
formerly referred to as non-alcoholic fatty liver disease (NAFLD).
An estimated 24% of U.S. adults are living with MASLD or NAFLDi,
a metabolic disease linked to obesity, cardiovascular disease and
type 2 diabetes, all of which pose significant public health
concerns. Adults with MASLD are not only at risk of developing
severe liver complications, such as cirrhosis and metabolic
dysfunction-associated steatohepatitis (MASH), but are also at risk
of cardiovascular disease, which is the leading cause of death in
people living with MASLDii. MASLD is commonly asymptomatic until it
progresses to advanced liver fibrosis, and the current gold
standard for diagnosis is a liver biopsy, which is invasive and
costly. As such, early diagnosis of MASLD could benefit patients
and the healthcare system.
While AI assessment of medical imaging offers a reliable,
non-invasive, large-scale approach to support clinicians in the
assessment of hepatic steatosis (fatty liver), it has traditionally
been difficult to assess liver attenuation on contrast-enhanced
scans – which make up a large proportion of CT scans – limiting the
ability of clinicians to detect non-severe cases of MASLDiii.
HealthFLD was designed to help clinicians in the assessment and
analysis of fatty liver in the general population from routine CT
scans.
Amidst rising obesity rates, the prevalence of
liver-related disease is growing, and the need for an approved
treatment for MASH has yet to be met. With several late-stage drug
candidates for MASH in development and the availability of GLP-1
drugs for the management of type 2 diabetes and other metabolic
diseases, identification of liver steatosis is especially
relevant.
"We are proud to offer HealthFLD as the third
product of Nanox AI’s suite of cutting-edge, AI-powered population
health solutions designed to confront chronic diseases of great
public health concern head-on and potentially improve health
outcomes,” said Erez Meltzer, Chief Executive Officer of Nanox.
“Furthermore, we believe that AI innovative solutions, and
specifically HealthFLD, may deliver substantial advantages to the
biopharmaceutical industry to streamline the identification of
candidates for clinical trials of much-needed therapies for liver
diseases including MASH. This regulatory decision solidifies our
leadership as a developer of automated AI software medical
devices.”
In a retrospective 2023 study of 2,917 patients,
published in the American Journal of Roentgenology (AJR), the
HealthFLD AI software demonstrated high performance in the
detection of at least moderate hepatic steatosis in
contrast-enhanced CT scans, with a sensitivity of 77.8% and
specificity of 93.2% at less than 80 HU. Medical imaging offers the
only reliable noninvasive method for quantifying liver fat.
Integrating HealthFLD with widely used standard CT scans offers
clinicians the potential to opportunistically screen for liver
steatosis and possible signs of MASLD on a population level. “In
recent years, automated, deep learning tools have offered an
efficient, low-cost tool used to detect diseases in earlier
stages,” said Perry J. Pickhardt, MD, of the University of
Wisconsin School of Medicine & Public Health, and lead author
of the AJR study. “We are now at a watershed moment when metabolic
diseases are growing in prevalence and more effective treatment
options are becoming available. It’s promising to have a liver
solution available that may help evaluate early signs of illness
from routine imaging.”
The HealthFLD clearance is the third product
across the Nanox AI suite of population health solutions to receive
FDA clearance. The FDA previously cleared HealthCCSng, a solution
that detects coronary artery calcium (CAC) that presents a risk for
coronary artery disease, and HealthOST, a solution that assesses
vertebral compression fractures and bone mineral density to support
clinicians in the evaluation and assessment of musculoskeletal
disease of the spine (such as osteoporosis).
About Metabolic
Dysfunction-Associated Steatotic Liver Disease (MASLD)
Metabolic dysfunction-associated steatotic liver
disease (MASLD), formerly referred to as non-alcoholic fatty liver
disease (NAFLD), refers to a group of metabolic conditions linked
to obesity, cardiovascular disease and type 2 diabetes. An
estimated 30% of the adult population globally has MASLD,iv a major
risk factor for chronic liver disease and for cardiovascular
disease, which is the leading cause of mortality in this patient
population.v
About Nanox AI Nanox AI is
the deep-learning medical imaging analytics subsidiary of Nanox.
Nanox.AI solutions are developed to target highly prevalent chronic
and acute diseases affecting large populations around the world.
Leveraging AI technology, Nanox AI helps clinicians extract
valuable and actionable clinical insights from routine medical
imaging that otherwise may go unnoticed, potentially initiating
further medical assessment to establish individual preventative
care pathways for patients. For more information, please visit
https://www.nanox.vision/ai.
About Nanox
Nanox (NASDAQ: NNOX) is focused on applying its
proprietary medical imaging technology and solutions to make
diagnostic medicine more accessible and affordable across the
globe. Nanox’s vision is to increase access, reduce costs and
enhance the efficiency of routine medical imaging technology and
processes, in order to improve early detection and treatment, which
Nanox believes is key to helping people achieve better health
outcomes, and, ultimately, to save lives. The Nanox ecosystem
includes Nanox.ARC— a multi-source Digital Tomosynthesis system
that is cost-effective and user-friendly; an AI-based suite of
algorithms that augment the readings of routine CT imaging to
highlight early signs often related to chronic disease (Nanox.AI);
a cloud-based infrastructure (Nanox.CLOUD); and a proprietary
decentralized marketplace, through Nanox’s subsidiary, USARAD
Holdings Inc., that provides remote access to radiology and
cardiology experts; and a comprehensive teleradiology services
platform (Nanox.MARKETPLACE). Together, Nanox’s products and
services create a worldwide, innovative, and comprehensive solution
that connects medical imaging solutions, from scan to diagnosis.
For more information, please visit www.nanox.vision.
Forward-Looking Statements
This press release contains historical
information and forward-looking statements within the meaning of
The Private Securities Litigation Reform Act of 1995 with respect
to the business, financial condition and results of operations of
Nanox. All statements that are not historical facts contained in
this press release are forward-looking statements. Such statements
include, but are not limited to, any statements relating to the
initiation, timing, progress and results of the Company’s research
and development, manufacturing, and commercialization activities
with respect to its X-ray source technology and the Nanox.ARC, the
ability to realize the expected benefits of its recent acquisitions
and the projected business prospects of the Company and the
acquired companies. In some cases, you can identify forward-looking
statements by terminology such as the words “will,” “believe,”
“expect,” “intend,” “plan,” “should,” “estimate”, “might”, “may”,
“should”, “anticipate”, “expect”, “predict”’ “potential” and
similar expressions which are intended to identify forward-looking
statements. Forward-looking statements are based on information the
Company has when those statements are made or management’s good
faith belief as of that time with respect to future events and are
subject to risks and uncertainties that could cause actual
performance or results to differ materially from those expressed in
or suggested by the forward-looking statements. Factors that could
cause actual results to differ materially from those currently
anticipated include: risks related to (i) Nanox’s ability to
complete development of the Nanox System; (ii) Nanox’s ability to
successfully demonstrate the feasibility of its technology for
commercial applications; (iii) Nanox’s expectations regarding the
necessity of, timing of filing for, and receipt and maintenance of,
regulatory clearances or approvals regarding its technology, the
Nanox.ARC and Nanox.CLOUD from regulatory agencies worldwide and
its ongoing compliance with applicable quality standards and
regulatory requirements; (iv) Nanox’s ability to realize the
anticipated benefits of the acquisitions, which may be affected by,
among other things, competition, brand recognition, the ability of
the acquired companies to grow and manage growth profitably and
retain their key employees; (v) Nanox’s ability to enter into and
maintain commercially reasonable arrangements with third-party
manufacturers and suppliers to manufacture the Nanox.ARC; (vi) the
market acceptance of the Nanox System and the proposed pay-per-scan
business model; (vii) Nanox’s expectations regarding collaborations
with third-parties and their potential benefits; (viii) Nanox’s
ability to conduct business globally; (ix) changes in global,
political, economic, business, competitive, market and regulatory
forces; (x) risks related to the current war between Israel and
Hamas and any worsening of the situation in Israel; (xi) risks
related to business interruptions resulting from the COVID-19
pandemic or similar public health crises, among other things; and
(xii) potential litigation associated with our
transactions.
For a discussion of other risks and
uncertainties, and other important factors, any of which could
cause Nanox’s actual results to differ from those contained in the
Forward-Looking Statements, see the section titled “Risk Factors”
in Nanox’s Annual Report on Form 20-F for the year ended December
31, 2022, and subsequent filings with the U.S. Securities and
Exchange Commission. The reader should not place undue reliance on
any forward-looking statements included in this press release.
Except as required by law, Nanox undertakes no
obligation to update publicly any forward-looking statements after
the date of this press release to conform these statements to
actual results or to changes in the Company’s expectations.
CONTACTS:
Media Contact: Ben ShannonICR
WestwickeNanoxPR@icrinc.com
Investor Contact: Mike CavanaughICR
Westwickemike.cavanaugh@westwicke.com
i Younossi ZM, Koenig AB, Abdelatif D, Fazel Y, Henry L, Wymer
M. Global epidemiology of nonalcoholic fatty liver
disease—meta-analytic assessment of prevalence, incidence, and
outcomes. Hepatology. 2016;64(1):73–84. doi:10.1002/hep.28431ii
Dulai PS, Singh S, Patel J, Soni M, Prokop LJ, Younossi Z, et al.
Increased risk of mortality by fibrosis stage in nonalcoholic fatty
liver disease: systematic review and meta-analysis. Hepatology
2017;65:1557-65.iii Pickhardt PJ, Blake GM, Kimmel Y, et al.
Detection of Moderate Hepatic Steatosis on Portal Venous Phase
Contrast-Enhanced CT: Evaluation Using an Automated Artificial
Intelligence Tool. Amer Jour Roentgen 2023;221(6): 748 – 758.iv Le
MH, Yeo YH, Li X, Li J, Zou B, Wu Y, et al. 2019 Global NAFLD
prevalence: a systematic review and meta-analysis. Clin
Gastroenterol Hepatol 2022;20:2809-17.v Dulai PS, Singh S, Patel J,
Soni M, Prokop LJ, Younossi Z, et al. Increased risk of mortality
by fibrosis stage in nonalcoholic fatty liver disease: systematic
review and meta-analysis. Hepatology 2017;65:1557-65.
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