GlucoTrack, Inc.
7.30+0.56 (+8.23%)
Oct 28, 4:00:01 PM EDT · NasdaqCM · GCTK · USD
Key Stats
Market Cap
6.65MP/E (TTM)
-Basic EPS (TTM)
-2441.21Dividend Yield
0%Recent Filings
8-K
8-K
Glucotrack issues $3M note
Glucotrack secured $3 million in funding on September 12, 2025, via a zero-interest convertible promissory note with a $3.6 million principal, carrying a $600,000 original issue discount; it matures in 12 months or upon a qualified financing exceeding $5 million, with conversion at the financing price but no lower than $4.87 per share. Proceeds tie to an existing $20 million equity line of credit, mandating full repayment from initial draws until stockholder approval, then half thereafter. This bolsters liquidity while granting the investor a 25% participation right in future offerings. Default risks include bankruptcy triggers demanding immediate repayment.
8-K
Glucotrack secures $20M equity line
Glucotrack inked a deal on September 11, 2025, with Sixth Borough Capital Fund for up to $20 million in common stock sales over 24 months, via regular, add-on, and intraday purchases at discounted VWAP rates. The pact includes a 1.5% commitment fee payable in cash or shares, with proceeds earmarked for working capital and general corporate needs. Yet dilution looms large, capped initially at 19.99% of outstanding shares without stockholder nod.
8-K
Q2 2025 results and CBGM progress
Glucotrack reported a $11.6 million net loss for the six months ended June 30, 2025, up from $7.4 million last year, driven by a $3.3 million non-cash derivative liability charge and higher operating expenses, yet bolstered cash to $9.6 million via equity raises. The company advanced its implantable CBGM with positive first-in-human study results showing 7.7% MARD accuracy and no serious adverse events. On track for Australian trial implants in Q3 2025. Cash funds operations through year-end.
10-Q
Q2 FY2025 results
Glucotrack posted an operating loss of $4.8M for Q2 FY2025 ended June 30, 2025, up 6.8% y/y from $4.5M yet down from $3.4M in Q1 (derived), driven by higher general and administrative costs on legal fees and personnel, while research expenses dipped 12.2% y/y to $3.2M amid lower manufacturing accruals. Net loss widened to $4.8M from $4.5M y/y, with the gap to operating loss under 20% tied to a $95K warrant repurchase loss. Cash swelled to $9.6M after $10.7M from equity offerings, funding a first-in-human study that hit all endpoints with 7.7% MARD accuracy; a long-term trial starts Q3 outside the US, with FDA IDE filing eyed for Q4. Cash burn hit $6.7M YTD, no FCF as capex was minor. Reverse splits in February and June adjusted shares. Regulatory hurdles could stall trials.
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