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Glucotrack Reports First Quarter 2026 Financial Results and Recent Corporate Highlights

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Glucotrack (Nasdaq:GCTK) reported first quarter 2026 results and progress on its fully implantable continuous blood glucose monitoring (CBGM) program.

Key updates include FDA IDE submission for a U.S. clinical study targeted for 2H 2026, supportive peer-reviewed data, debt reduction, and lower net loss year-over-year.

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

Positive

  • Submitted FDA IDE for U.S. clinical study of fully implantable CBGM, targeting 2H 2026 start
  • Peer-reviewed data showed 6.8% MARD and 240-day sensor stability in ovine CBGM study
  • Reduced $3.6 million promissory note balance to approximately $1.6 million
  • Net loss decreased to $4.3 million from $6.8 million year-over-year
  • Other expense declined to $0.1 million from $3.3 million year-over-year
  • Equity line draw of approximately $1.0 million post-quarter strengthened liquidity

Negative

  • Research and development expenses increased to $2.1 million from $1.9 million
  • General and administrative expenses rose to $2.1 million from $1.6 million
  • Cash and cash equivalents declined to $3.9 million from $7.4 million since year-end
  • Company expects existing cash to fund operations only into early third quarter 2026

News Market Reaction – GCTK

-2.97%
5 alerts
-2.97% News Effect
-7.5% Trough in 38 hr 9 min
-$42K Valuation Impact
$1.36M Market Cap
46.24K Volume

On the day this news was published, GCTK declined 2.97%, reflecting a moderate negative market reaction. Argus tracked a trough of -7.5% from its starting point during tracking. Our momentum scanner triggered 5 alerts that day, indicating moderate trading interest and price volatility. This price movement removed approximately $42K from the company's valuation, bringing the market cap to $1.36M at that time.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement combines Q1 2026 financials with key CBGM milestones, including IDE submission and...
Analysis

This announcement combines Q1 2026 financials with key CBGM milestones, including IDE submission and supportive long-term accuracy data with a 6.8% MARD over 240 days. Net loss narrowed to $4.3M, but cash fell to $3.9M with stated runway into early Q3 2026, underscoring financing dependence. Investors may watch IDE progress, upcoming clinical data, and potential share sales under existing registered resale capacity as drivers of future dilution and execution risk.

Key Figures

R&D expenses Q1 2026: $2.1 million G&A expenses Q1 2026: $2.1 million Net loss Q1 2026: $4.3 million +5 more
8 metrics
R&D expenses Q1 2026 $2.1 million Quarter ended March 31, 2026
G&A expenses Q1 2026 $2.1 million Quarter ended March 31, 2026
Net loss Q1 2026 $4.3 million vs. $6.8 million in Q1 2025
Cash balance $3.9 million As of March 31, 2026 (vs. $7.4M on Dec 31, 2025)
Promissory note balance $1.6 million Reduced from $3.6 million via debt-for-equity exchange
Equity line draw Approximately $1.0 million Drawn after quarter-end under equity line facility
Cash used in operations $4.1 million Q1 2026 operating cash outflow
MARD 6.8% In-vivo ovine CBGM study over 240 days

Previous Earnings Reports

5 past events · Latest: Mar 30 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Mar 30 FY 2025 earnings Positive -14.1% Reported 2025 results, new patents, cash of $7.4M, and IDE plan.
Nov 13 Q3 2025 earnings Positive -8.6% Secured new financing, higher cash, and outlined IDE and trial plans.
Aug 14 Q2 2025 earnings Positive +0.9% Detailed Australia feasibility study, strong MARD data, and $9.6M cash.
May 14 Q1 2025 earnings Neutral +0.1% Advanced CBGM plans with higher net loss and a stronger cash position.
Mar 31 FY 2024 earnings Positive +28.9% First human CBGM study success, higher R&D and losses, and $5.6M cash.

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

Pattern Detected

Earnings releases often came with sizable price swings, frequently negative despite generally constructive operational updates, suggesting a history of volatile and sometimes contrarian reactions around results.

Recent Company History

Over the last year, Glucotrack’s earnings updates have mixed financing steps, CBGM development progress, and growing losses. In 2024, the company transitioned to clinical stage with a first human CBGM study and raised $16.3M, yet shares jumped only around some reports. Subsequent quarters in 2025 highlighted new studies, added advisors, and cash balances between roughly $5.6M–$9.6M, but several earnings days saw notable declines. Today’s Q1 2026 release continues that pattern of operational progress alongside ongoing losses and financing dependence.

Key Terms

investigational device exemption (ide), u.s. food and drug administration (fda), continuous blood glucose monitoring (cbgm), mean absolute relative difference (mard), +2 more
6 terms
investigational device exemption (ide) regulatory
"Submitted Investigational Device Exemption (IDE) application to the U.S. Food and Drug Administration"
An investigational device exemption (IDE) is a regulatory permission that allows a medical device to be used in clinical studies so companies can gather safety and effectiveness data before full market approval. For investors, an IDE is a key milestone because it lets a company test real-world performance and move toward commercial clearance or approval—much like a trial run that, if successful, can unlock larger revenue opportunities and reduce regulatory risk.
u.s. food and drug administration (fda) regulatory
"Submitted Investigational Device Exemption (IDE) application to the U.S. Food and Drug Administration"
The U.S. Food and Drug Administration (FDA) is a government agency responsible for protecting public health by ensuring the safety and effectiveness of food, medicines, vaccines, and other health-related products. For investors, the FDA’s decisions can significantly impact companies in the healthcare and food industries, as approval or rejection of products can influence a company's success and stock performance.
continuous blood glucose monitoring (cbgm) medical
"fully implantable continuous blood glucose monitoring (CBGM) technology"
Continuous blood glucose monitoring (cbgm) is a wearable medical system that measures a person’s blood sugar levels automatically and continuously throughout the day using a small sensor under the skin and a reader or smartphone. For investors, cbgm matters because its adoption drives recurring device and subscription revenue, affects regulatory and reimbursement risk, and signals market demand for related technologies and data services—similar to how smart meters changed utility billing and customer insights.
mean absolute relative difference (mard) medical
"The in-vivo ovine study showed a 6.8% Mean Absolute Relative Difference (MARD)"
Mean absolute relative difference (MARD) is a numerical measure of how far a series of measurements deviate, on average, from a trusted reference, expressed as a percentage. For medical devices (commonly glucose monitors) it summarizes typical percent error between device readings and lab measurements; investors use it as a simple gauge of accuracy and reliability, which can affect regulatory approval, clinical adoption, customer trust and ultimately sales — like knowing how many percent a thermometer is usually off.
promissory note financial
"reduced the outstanding balance of its $3.6 million promissory note to approximately $1.6 million"
A promissory note is a written IOU in which one party promises to pay a specific sum, often with interest, to another party by a set date or on demand. Investors care because it functions like a loan: it creates a legal claim on future cash flows, carries credit and timing risk, and can affect valuation or liquidity—think of it as a formal, tradable promise to be repaid that can be assessed like any other debt investment.
equity line of credit financial
"drew approximately $1.0 million under its existing equity line of credit facility"
An equity line of credit is a loan that allows homeowners to borrow money against the value of their property, similar to having a flexible credit card secured by their home. It matters to investors because it provides a way for property owners to access cash for various needs, which can influence real estate markets and overall economic activity. This type of credit offers ongoing borrowing capacity, making it a valuable financial tool for those with significant property equity.

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

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Submitted Investigational Device Exemption (IDE) application to the U.S. Food and Drug Administration (FDA) to initiate a U.S. clinical study for fully implantable continuous blood glucose monitoring (CBGM) technology

Company targeting U.S. clinical trial launch in second half of 2026

Peer-Reviewed Studies published in The Journal of Diabetes Research and in the Institute of Electrical and Electronics Engineers (IEEE) Sensors Journal support advancement of Company’s implantable CBGM technology

Rutherford, NJ, May 14, 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 reported financial results and recent corporate highlights for the first quarter ended March 31, 2026.

“During the quarter, we made meaningful progress advancing our CBGM program while further strengthening our foundation as a company,” said Paul V. Goode, PhD, President and Chief Executive Officer of Glucotrack. “We successfully completed our presub process with FDA, culminating in the submission of our IDE to the FDA, an important milestone that brings us closer to initiating U.S. clinical studies. We also published two key sets of preclinical and in-vitro data in peer-reviewed journals, further supporting the development of our technology, and strengthened our balance sheet by reducing debt and extending our financial runway.”

First Quarter 2026 & Recent Highlights

Corporate Highlights

  • The Company held its third Patient Advisory Board (PAB) meeting during which patients shared perspectives on diabetes device prescribing and initiation, as well as their experiences with healthcare provider education and preparedness.
  • Strengthened balance sheet with debt reduction. The Company reduced the outstanding balance of its $3.6 million promissory note to approximately $1.6 million, primarily through the exchange of a portion of the note into shares of common stock at market price. Subsequent to quarter end, the Company drew approximately $1.0 million under its existing equity line of credit facility, further strengthening its cash position.

Advanced Product and Clinical Development

  • The Company successfully submitted its IDE application to the FDA to initiate a U.S. clinical study for its fully implantable CBGM technology. The submission represents a key milestone in advancing the Company's CBGM technology into U.S. clinical evaluation, supported by several years of focused engineering, preclinical evaluation, and iterative design work.
  • In a peer-reviewed article titled, “Year-Long Measurement of Glucose Oxidase Deactivation in Electrochemical Glucose Sensors,” published in the IEEE Sensors Journal, the Company reported data validating the long-term stability of its glucose oxidase sensor, providing foundational scientific evidence to support the device’s intended three-year longevity.
  • In a peer-reviewed article titled, “In Vivo Evaluation of a Novel Long-Term Intravascular Implantable Continuous Blood Glucose Monitor in an Ovine Model: A Glucotrack Inc. Investigation,” published in The Journal of Diabetes Research, the Company reported data demonstrating the long-term accuracy and stability of the Company’s fully implantable CBGM system. The in-vivo ovine study showed a 6.8% Mean Absolute Relative Difference (MARD) and sustained sensor performance over 240 days, supporting the platform’s progression toward clinical studies.

Anticipated Milestones

  • Initiate U.S. clinical study of the Company’s CBGM in 2H 2026.
  • Present clinical data demonstrating the safety and accuracy of the CBGM technology at additional industry conferences, with timing and venues to be determined as data become available.
  • Continue to gain insight from patients living with diabetes on current management challenges and receive feedback on Glucotrack’s product development and commercialization strategies through additional PAB meetings.

Financial Results for the Quarter ended March 31, 2026

Research and Development Expenses: Research and development expenses were $2.1 million for first quarter of 2026 compared to $1.9 million for first quarter of 2025. The increase of $0.2 million was primarily due to timing in product and manufacturing development activities.

General and Administrative Expenses: General and Administrative expenses were $2.1 million for the first quarter of 2026 compared to $1.6 million for first quarter of 2025. The increase of $0.5 million was primarily attributable to increased professional fees and personnel costs.

Other (Income) Expense, Net: Other expense was $0.1 million for the first quarter 2026, as compared to $3.3 million for the first quarter of 2025. The decrease in other expense is primarily attributed to the current year’s reduction in the change of derivative liabilities.

Net Loss: Net loss for the first quarter of 2026 was $4.3 million compared to a net loss of $6.8 million for the first quarter of 2025. The decrease in net loss is primarily attributed to the non-cash change in derivative liabilities.

Cash Position: Cash and cash equivalents as of March 31, 2026, were $3.9 million, compared with $7.4 million in cash and cash equivalents as of December 31, 2025. The net decrease in cash and cash equivalents was attributable to $4.1 million of cash used in operating activities offset by net proceeds received from financing activities of $0.6 million.

Based on current plans and assumptions, the Company believes that its existing cash and cash equivalents will provide sufficient runway into early 3Q 2026, allowing for the initiation of its U.S. human clinical trial shortly thereafter.

The Glucotrack Continuous Blood Glucose Monitor is an Investigational Device and is limited by federal (or United States) law to investigational use.

For more information about Glucotrack’s CBGM, 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.

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:Media:
investors@glucotrack.comGlucotrackPR@icrinc.com


GLUCOTRACK INC.

CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands of US dollars except share data)

  In thousands of US dollars

(except stock data)
 
  March 31,

2026
  December 31,

2025
 
  Unaudited    
Current Assets        
Cash and cash equivalents $3,929  $7,383 
Other current assets  285   284 
Total current assets  4,214   7,667 
         
Operating lease right-of-use asset, net  26   33 
Property and equipment, net  116   138 
TOTAL ASSETS $4,356  $7,838 
         
LIABILITIES AND STOCKHOLDERS’ (DEFICIT) EQUITY        
Current Liabilities        
Accounts payable $1,299  $1,317 
Operating lease liability, current  26   28 
Promissory notes  3,330   3,182 
Other current liabilities  320   246 
Total current liabilities  4,975   4,773 
         
Non-Current Liabilities        
Derivative financial liabilities  -   1 
Operating lease liability, non-current  -   5 
Loans from stockholders  232   231 
Total liabilities  5,207   5,010 
         
Commitments and contingent liabilities (Note 5)        
         
Stockholders’ Equity (Deficit)        
Common Stock of $0.001 par value (“Common Stock”):        
250,000,000 shares authorized as of March 31, 2026 and as of December 31, 2025; 2,524,279 and 910,688 shares issued and outstanding as of March 31, 2026 and December 31, 2025, respectively  3   1 
         
Additional paid-in capital  155,274   151,080 
Receipts on account of shares  -   3,544 
Accumulated other comprehensive income  44   41 
Accumulated deficit  (156,172)  (151,838)
Total stockholders’ equity (deficit)  (851)  2,828 
         
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT) $4,356  $7,838 


GLUCOTRACK INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
(in thousands of US dollars except share data) (unaudited)

  Three-month period ended

March 31,
 
  2026  2025 
Operating expenses:        
Research and development $2,132  $1,871 
General and administrative  2,071   1,627 
Total operating expenses  4,203   3,498 
Loss from operations  4,203   3,498 
Other (income) expense:        
Change in fair value of derivative liabilities  (1)  3,376 
Other (income) expense, net  132   (4)
Finance expenses (income), net  -   (37)
Total other (income) expense  131   3,335 
Net Loss  4,334   6,833 
Other comprehensive income:        
Foreign currency translation adjustment  (3)  (36)
Comprehensive loss for the period $4,331  $6,797 
Basic and diluted loss per share $2.65  $40.14 
Weighted average number of Common Stock outstanding used in computing basic and diluted loss per share  1,638,128   169,345 



FAQ

What did Glucotrack (GCTK) report for its Q1 2026 net loss?

Glucotrack reported a Q1 2026 net loss of $4.3 million, compared with $6.8 million in Q1 2025. According to Glucotrack, the smaller loss mainly reflects a lower non-cash change in derivative liabilities rather than reduced operating spending.

How did Glucotrack (GCTK) Q1 2026 operating expenses change year-over-year?

Glucotrack’s Q1 2026 research and development and general and administrative expenses both rose year-over-year. According to Glucotrack, R&D increased to $2.1 million from $1.9 million and G&A rose to $2.1 million from $1.6 million, driven by development timing and higher professional and personnel costs.

What clinical progress did Glucotrack (GCTK) announce for its implantable CBGM in May 2026?

Glucotrack submitted an Investigational Device Exemption (IDE) to the FDA to start a U.S. CBGM study, targeting launch in 2H 2026. According to Glucotrack, peer-reviewed data showed 6.8% MARD and 240-day performance in an ovine model, supporting advancement toward human trials.

What is Glucotrack (GCTK) cash position and runway after Q1 2026?

Glucotrack ended March 31, 2026 with $3.9 million in cash and cash equivalents, down from $7.4 million at year-end 2025. According to Glucotrack, existing cash is expected to fund operations into early third quarter 2026, supporting U.S. trial initiation shortly afterward.

How did Glucotrack (GCTK) strengthen its balance sheet in Q1 2026?

Glucotrack reduced the outstanding balance of its $3.6 million promissory note to about $1.6 million, mainly by exchanging debt for common stock at market price. According to Glucotrack, it also drew roughly $1.0 million from its existing equity line after quarter end.

What peer-reviewed results support Glucotrack (GCTK) implantable CBGM technology?

Glucotrack reported long-term sensor stability and performance in two peer-reviewed articles. According to Glucotrack, IEEE Sensors Journal data support three-year sensor longevity, while a Journal of Diabetes Research ovine study showed 6.8% MARD and sustained function over 240 days, backing progression to clinical studies.