Full Press Release Details
REPORTS SUCCESSFUL COMPLETION OF FIRST REPORTED LONG-TERM PRECLINICAL STUDY OF ITS EPIDURAL GLUCOSE MONITORING SENSOR
of the novel epidural continuous glucose monitoring study confirms its potential for providing simplified disease management for patients
with painful diabetic neuropathy
NJ, June 13, 2024 (GLOBE NEWSWIRE) - Glucotrack, Inc. (Nasdaq: GCTK) ("Glucotrack" or the "Company"),
a medical device company focused on the design, development, and commercialization of novel technologies for people with diabetes, today
announced that its implantable continuous glucose monitor has successfully completed a 60-day long-term preclinical study demonstrating
the feasibility of glucose monitoring in the epidural space.
Glucotrack sensor, implanted in the epidural space of animals, closely tracked glucose values from both a commercially available blood
glucose monitor and a subcutaneous continuous glucose monitor (CGM) throughout the 60-day period. No abnormal clinical signs were observed
throughout the study period, and no abnormal findings were observed in the spinal cord or surrounding tissues during post-explant analysis.
The study also confirmed that the implanted sensor did not cause any delayed latent effects over the long-term period, which is particularly
important as a complete healing process in animal studies with implanted devices may take several weeks.
"With the successful completion of this long-term study, we are confident in the performance of our epidural sensor, and we are
excited to be an innovator in epidural glucose monitoring. We are now exploring opportunities for continued development and application
of our novel technology to benefit people living with diabetes," said Paul V. Goode, PhD, CEO of Glucotrack.
previously announced interim performance and safety results from this long-term animal study assessing sustained epidural glucose
monitoring performance. With the completion of this study, the durability of the epidural approach for continuous glucose monitoring
has now been confirmed over the 60-day period.
is a progressive neurological disorder that affects approximately one-fifth of the more than 38 million Americans with diabetes, equating
to more than 7 million individuals.1,2 The Company believes that, if approved, a continuous glucose monitoring system that
takes readings in the epidural space may be integrated with existing treatments for these patients, simplifying their device and disease
more information about Glucotrack, visit glucotrack.com. Information on the Company's website does not constitute a part
of and is not incorporated by reference into this press release.
Abbott CA, Malik RA, van Ross ER, Kulkarni J,
Boulton AJ. Prevalence and characteristics of painful diabetic neuropathy in a large community-based diabetic population in the
U.K. Diabetes Care 2011;34:2220-2224.
Centers for Disease Control and Prevention. (2022). National Diabetes Statistics Report website. https://www.cdc.gov/diabetes/data/statistics-report/index.html
Inc. (NASDAQ: GCTK) is focused on the design, development, and commercialization of novel technologies for people with diabetes. The
Company is currently developing a long-term implantable continuous blood glucose monitoring system for people living with diabetes.
CBGM is a long-term, implantable system that continually measures blood glucose levels with a sensor longevity of 2+ years, no on-body
wearable component and with minimal calibration. For more information, please visit http://www.glucotrack.com.
news release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Statements
contained in this news release that are not statements of historical fact may be deemed to be forward-looking statements. Without limiting
the generality of the foregoing, words such as "believe", "expect", "plan" and "will"
are intended to identify forward-looking statements. Such forward-looking statements are based on the beliefs of management, as well
as assumptions made by, and information currently available to, management. These statements relate only to events as of the date on
which the statements are made, and Glucotrack undertakes no obligation to publicly update any forward-looking statements, whether as
a result of new information, future events or otherwise, except as required by law. All of the forward-looking statements made in this
press release are qualified by these cautionary statements, and there can be no assurance that the actual results anticipated by Glucotrack
will be realized or, even if substantially realized, that they will have the expected consequences to or effects on us or our business
or operations. Readers are cautioned that certain important factors may affect Glucotrack's actual results and could cause such
results to differ materially from any forward-looking statements that may be made in this news release. Factors that may affect Glucotrack's
results include, but are not limited to, the ability of Glucotrack to raise additional capital to finance its operations (whether through
public or private equity offerings, debt financings, strategic collaborations or otherwise); risks relating to the receipt (and timing)
of regulatory approvals (including U.S. Food and Drug Administration approval); risks relating to enrollment of patients in, and the
conduct of, clinical trials; risks relating to Glucotrack's future distribution agreements; risks relating to its ability to hire
and retain qualified personnel, including sales and distribution personnel; and the additional risk factors described in Glucotrack's
filings with the U.S. Securities and Exchange Commission (the "SEC"), including its Annual Report on Form 10-K for the year
ended December 31, 2023 as filed with the SEC on March 28, 2024.