STOCK TITAN

Glucotrack to Highlight Implantable Continuous Blood Glucose Monitoring Technology at the American Diabetes Association’s 2026 Scientific Sessions

(Moderate)
(Positive)
Tags

Glucotrack (Nasdaq:GCTK) will showcase its fully implantable continuous blood glucose monitoring (CBGM) technology at the American Diabetes Association’s 2026 Scientific Sessions in New Orleans, June 5–8, 2026.

The company highlights direct blood measurements, multi-year implant longevity, no on-body wearables, new peer-reviewed data, and a recent FDA IDE submission.

Loading...
Loading translation...

Positive

  • None.

Negative

  • None.

News Market Reaction – GCTK

+18.92%
14 alerts
+18.92% Session close to close
+36.4% Peak in 23 hr 8 min
$4.57M Market Cap
0.1x Rel. Volume

In the May 26 session, GCTK gained 18.92%, reflecting a significant positive market reaction. Argus tracked a peak move of +36.4% during that session. Our momentum scanner triggered 14 alerts that day, indicating notable trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock surged +18.9% in the session following this news. A strong positive reaction aligns with t...
Analysis

The stock surged +18.9% in the session following this news. A strong positive reaction aligns with the constructive nature of this update, which showcases Glucotrack’s implantable CBGM platform and highlights prior data such as a 6.8% MARD over 240 days and multiple peer‑reviewed publications. However, the stock still trades 96.86% below its 52‑week high and under its 3.78 200‑day MA. An effective S-3 registering 3,224,803 resale shares also signals notable potential dilution and overhang.

Key Figures

Conference dates: June 5–8, 2026 Presentation time: 2:10–2:30 p.m. CDT MARD: 6.8% +5 more
8 metrics
Conference dates June 5–8, 2026 ADA 2026 Scientific Sessions in New Orleans
Presentation time 2:10–2:30 p.m. CDT ADA 2026 Innovation Hub session on June 6
MARD 6.8% Ovine model accuracy over 240 days and 79 glucose tolerance tests
Study duration 240 days Ovine model study period for implantable CBGM sensor
Glucose tolerance tests 79 tests Intravenous glucose tolerance tests in ovine accuracy study
Peer-reviewed studies 2 publications April 2026 publications supporting long-term sensor design
Price vs 52-week high -96.86% Current price relative to 52-week high of 15.9
Price vs 52-week low 15.98% Current price above 52-week low of 0.4311

Historical Context

5 past events · Latest: May 14 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 14 Earnings and IDE update Positive -3.0% Reported Q1 2026 results, debt reduction, and IDE progress for U.S. study.
May 07 IDE submission Positive +0.8% Filed FDA IDE application to initiate U.S. clinical study of CBGM system.
Apr 30 Ovine accuracy study Positive -7.3% Published ovine study showing long‑term accuracy and stability of implantable CBGM.
Apr 21 Sensor longevity study Positive -4.0% Published IEEE Sensors Journal data supporting long‑life implantable sensor design.
Mar 30 FY25 earnings and financing Positive -14.1% Reported 2025 results, new patents, $4.0M placement, and planned IDE filing timeline.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Positive development and data releases have often seen weak or negative next-day price reactions, with only the IDE submission showing a modest gain.

Recent Company History

Over the last few months, Glucotrack reported earnings updates, multiple peer‑reviewed publications, and its FDA IDE submission for a U.S. clinical study. Despite fundamentally positive clinical and corporate milestones, four of the last five news events (from Mar 30 through May 14) were followed by negative 24‑hour price moves, including a -14.11% reaction to 2025 results. Today’s conference-focused announcement builds on April’s accuracy and sensor‑longevity data and the early‑May IDE filing.

Key Terms

continuous blood glucose monitoring, cbgm, investigational device exemption, mard, +1 more
5 terms
continuous blood glucose monitoring medical
"fully implantable continuous blood glucose monitoring (CBGM) technology at the American"
A continuous blood glucose monitoring system is a wearable sensor and accompanying device or app that measures a person’s blood-sugar level frequently throughout the day and night, sending real-time readings and alerts for highs or lows. For investors, these systems matter because they can drive steady product sales, recurring data or service revenue, and influence healthcare costs and treatment choices the same way a smart thermostat changes heating habits—wider adoption can reshape the market for diabetes care.
cbgm medical
"fully implantable continuous blood glucose monitoring (CBGM) technology at the American"
Capillary blood glucose monitoring (CBGM) is the common finger‑stick method that measures blood sugar from a tiny drop of capillary blood using a portable meter and test strip. For investors, CBGM matters because it drives demand, regulation and reimbursement in the diabetes device market—accuracy, cost and convenience determine which products succeed, much like fuel efficiency and price steer car buyers.
investigational device exemption regulatory
"Glucotrack submitted its Investigational Device Exemption application to the FDA earlier"
An investigational device exemption (IDE) is a regulatory permission that allows a medical device maker to test an unapproved device in people so the device’s safety and effectiveness can be studied. For investors, an IDE matters because it marks a formal step toward regulatory approval—like getting a temporary test-drive permit—and influences clinical cost, timelines, and the likelihood a device will reach the market and generate revenue.
mard medical
"demonstrating sustained accuracy with a 6.8% MARD over 240 days in an ovine model"
MARD (Mean Absolute Relative Difference) is a numerical measure of how far, on average, readings from a medical sensor or diagnostic device differ from a reference or true value, expressed as a percentage. Investors care because a lower MARD means more reliable and competitive products—similar to a scale that consistently shows weight close to the true number—affecting product adoption, regulatory acceptance and commercial success.
glucose oxidase medical
"study in the IEEE Sensors Journal demonstrating year-long glucose oxidase enzyme stability"
An enzyme that reacts with glucose to produce hydrogen peroxide and a small electrical or color change, making blood sugar levels measurable. Think of it as the tiny detector inside many glucose test strips and biosensors that turns sugar into a readable signal. Investors care because its performance, supply and regulatory approval directly affect companies that make diabetes tests, point‑of‑care devices, certain food processing steps and related biotech products.

AI-generated analysis. How Rhea-AI works. Not financial advice.

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google

RUTHERFORD, N.J., May 26, 2026 (GLOBE NEWSWIRE) -- Glucotrack, Inc. (Nasdaq: GCTK) (“Glucotrack” or the “Company”), a medical technology company focused on the design, development, and commercialization of novel technologies for people with diabetes, today announced that company leadership will present on its fully implantable continuous blood glucose monitoring (CBGM) technology at the American Diabetes Association’s (ADA) 2026 Scientific Sessions, taking place in New Orleans, June 5 – 8, 2026.

As part of the ADA’s Innovation Hub, Mark Tapsak, PhD, Glucotrack’s Chief Scientific Officer, will present on the potential of next-generation CGM technology that addresses unmet patient needs through direct blood measurements (providing more accurate readings), multi-year implant longevity, and a fully implantable design that eliminates on-body wearables.

Presentation Details:

  • Update on Continuous Blood Glucose Monitoring Technology
    • Date and Time: Saturday, June 6, 2:10 – 2:30 p.m. CDT
    • Location: Innovation Hub, ADA 2026

“We look forward to presenting at ADA’s Scientific Sessions,” said Paul V. Goode, PhD, President and Chief Executive Officer. “With our IDE submission now before the FDA and two peer-reviewed publications supporting our long-term sensor design, this is an important opportunity to share our progress and engage with the diabetes community on the future of continuous blood glucose monitoring.”

Glucotrack will also be available throughout the conference in the Innovation Hub of the Exhibit Hall.

Glucotrack has continued to advance its CBGM technology. In April 2026, the company published two peer-reviewed studies supporting its long-term sensor design: a study in the Institute of Electrical and Electronics Engineers Sensors Journal demonstrating year-long glucose oxidase enzyme stability and a study in The Journal of Diabetes Research demonstrating sustained accuracy with a 6.8% MARD over 240 days in an ovine model across 79 glucose tolerance tests. Building on this scientific foundation, Glucotrack submitted its Investigational Device Exemption application to the FDA earlier this month, marking a key step toward initiating a U.S. clinical study.

For more information about Glucotrack's CBGM, visit www.glucotrack.com.

About Glucotrack, Inc.

Glucotrack, 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.

Glucotrack’s Continuous Blood Glucose Monitor (CBGM) is a long-term, implantable system that continually measures blood glucose levels with a sensor longevity of 3 years, no on-body wearable component and with minimal calibration. The Glucotrack CBGM is an Investigational Device and is limited by federal (or United States) law to investigational use.

For more information, please visit http://www.glucotrack.com. Information on the Company’s website does not constitute a part of and is not incorporated by reference into this press release.

Forward-Looking Statements

This 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 “anticipate”, “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, 2025 as filed with the SEC on March 30, 2026.

Contacts: 
  
Investor Relations:
investors@glucotrack.com
Media:
GlucotrackPR@icrinc.com



FAQ

What CBGM technology will Glucotrack (Nasdaq:GCTK) present at the ADA 2026 Scientific Sessions?

Glucotrack will present a fully implantable continuous blood glucose monitoring (CBGM) technology using direct blood measurements. According to Glucotrack, key features include multi-year implant longevity, improved accuracy and a design that eliminates external on-body wearables for people living with diabetes.

When and where is Glucotrack (GCTK) presenting at the ADA 2026 Scientific Sessions?

Glucotrack is scheduled to present on Saturday, June 6, 2026, from 2:10–2:30 p.m. CDT. According to Glucotrack, the session takes place in the Innovation Hub at the American Diabetes Association’s 2026 Scientific Sessions in New Orleans.

What clinical data supports Glucotrack (GCTK) long-term CBGM sensor design?

Glucotrack reports two peer-reviewed studies supporting its long-term sensor design. According to Glucotrack, one study showed year-long glucose oxidase enzyme stability, and another reported 6.8% MARD accuracy over 240 days in an ovine model across 79 glucose tolerance tests.

What does Glucotrack’s FDA IDE submission mean for its CBGM technology?

Glucotrack recently submitted an Investigational Device Exemption (IDE) application to the FDA. According to Glucotrack, this filing is a key step toward initiating a U.S. clinical study of its fully implantable continuous blood glucose monitoring technology based on its long-term sensor design.

How could Glucotrack (GCTK) implantable CBGM address unmet diabetes care needs?

Glucotrack’s CBGM aims to address unmet needs through direct blood measurements and implant longevity. According to Glucotrack, the fully implantable design may improve accuracy, reduce maintenance and remove the need for external on-body wearables, potentially enhancing comfort and discretion for patients.

Will Glucotrack (GCTK) be available to meet attendees during ADA 2026?

Glucotrack plans to be available throughout the ADA 2026 conference in the Innovation Hub of the Exhibit Hall. According to Glucotrack, attendees can learn more about its implantable CBGM technology and recent scientific data during and beyond the scheduled presentation.