GALECTIN THERAPEUTICS INC (GALT) SEC Filings & Earnings Calls
EquiReason read 13 GALECTIN THERAPEUTICS INC SEC filings in the last 12 months. Latest: DEF 14A on 2026-10-13 — Proxy statement for 2026 annual meeting, including proposals to increase authorized shares and equity plan shares, and disclosure of Chairman's debt-to-equity conversion..
Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason
- Market cap
- 321.7M
- P/E TTM
- —
- Dividend yield
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- 52-week
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- Next earnings
- 16 Nov, in 23 days
Every filing, read
last 12 months · SECWhat happened, the numbers inside, guidance and risks. The original is one click away.
13 Oct 2026DEF 14AProxy statement for 2026 annual meeting, including proposals to increase authorized shares and equity plan shares, and disclosure of Chairman's debt-to-equity conversion.open
Figures in the filing · each found in the filing text
| Net Loss Applicable to Common Stockholders · FY2025 | $-31M |
Risks flagged
Dilution from authorized share increase
“To adopt and approve an amendment to our Restated Articles of Incorporation increasing the number of authorized common voting shares (“common stock”) from 150,000,000 to 250,000,000.” · word for word
Concentrated ownership and control by Chairman
“Richard E. Uihlein, the Company’s Chairman of the Board and largest stockholder, has provided the Company with various credit facilities to finance the Company’s working capital needs.” · word for word
14 Aug 202610-QFDA agreed on primary endpoint and regulatory path for potential full approval of belapectin in MASH cirrhosis; Phase 3 protocol to be filed in Q3 2026.open
Figures in the filing · each found in the filing text
| Cash and cash equivalents · Q2-2026 | $13M | |
| Net cash used in operations · H1-2026 | $6M | -56% y/y |
Risks flagged
Going concern uncertainty
“These factors raise substantial doubt about the Company’s ability to continue as a going concern for a period of 12 months from the issuance date of this Form 10-Q.” · word for word
Dependence on financing
“We will require more cash to fund our operations after June 2027. There can be no assurance that we will be successful in obtaining such new financing or, if available, that such financing will be on terms favorable to us.” · word for word
14 Aug 20268-K · 2.02Galectin Therapeutics reaches FDA agreement on Phase 3 trial design for belapectin in MASH cirrhosis; publishes positive NAVIGATE trial data in Hepatology; $105.8M debt converted to equity.open
Figures in the filing · each found in the filing text
| Cash and Cash Equivalents · Q2-2026 | $13M | |
| Research and Development Expenses · Q2-2026 | $2M | -36% y/y |
| General and Administrative Expenses · Q2-2026 | $2M | +29% y/y |
| Net Loss Applicable to Common Stockholders · Q2-2026 | $9M | |
| Debt Converted to Equity · Q2-2026 | $106M |
Risks flagged
Clinical trial risk; Phase 3 trial not yet initiated.
“Registrational Phase 3 trial protocol submission for belapectin is anticipated in 3Q 2026.” · word for word
Cash burn risk; cash runway only through June 2027.
“The Company believes it has sufficient cash to fund currently planned operations and research and development activities through June 2027.” · word for word
4 Aug 2026SC 13D/ARichard E. Uihlein converted ~$105.8M of debt into equity, increasing his beneficial ownership to 49.3% in Galectin Therapeutics, stated as for investment purposes without control intent.open
Figures in the filing · each found in the filing text
| Beneficial Ownership Percentage · 2026-07-31 | 49.3% |
Risks flagged
Concentrated ownership risk
“Richard E. Uihlein holds 49.3% beneficial ownership, giving significant control.”
4 Aug 20268-K · 3.02Issued 34.4M shares upon conversion of $105.8M debt to a single insider, increasing share count by ~52% and voting power to ~49%.share dilutionopen
Figures in the filing · each found in the filing text
| Converted debt principal · 2026-07-31 | $91M | |
| Converted accrued interest · 2026-07-31 | $15M | |
| Shares issued upon conversion · 2026-07-31 | 34,376,167 | |
| Total shares outstanding post-conversion · 2026-07-31 | 100,849,644 | |
| Blended average conversion price · 2026-07-31 | $3.07 |
Risks flagged
Insider control concentration risk: Chairman's voting power increases to ~49%, potentially enabling unilateral decisions.
“Mr. Uihlein beneficially owns approximately 44.3% of the outstanding voting power on an actual basis and approximately 49.3% of the outstanding voting power” · word for word
Dilution risk: Existing shareholders face ~52% dilution from this single transaction.
“issued 34,376,167 shares ... Company has approximately 100,849,644 shares of Common Stock”
Future registration risk: Shares are unregistered and subject to resale restrictions, but registration rights may lead to future selling pressure.
“Company is obligated to register the resale of such shares within 180 days of the conversion date” · word for word
4 Aug 2026SC 13D/ARichard E. Uihlein converted ~$105.8M of debt into equity, increasing his beneficial ownership to 49.3% in Galectin Therapeutics, stated as for investment purposes without control intent.open
Figures in the filing · each found in the filing text
| Beneficial Ownership Percentage · 2026-07-31 | 49.3% |
Risks flagged
Concentrated ownership risk
“Richard E. Uihlein holds 49.3% beneficial ownership, giving significant control.”
23 Jun 20268-K · 7.01Galectin Therapeutics announced positive Type C meeting with FDA, reaching agreement on primary endpoint and regulatory path for belapectin in MASH cirrhosis and portal hypertension; Phase 3 protocol submission planned for Q3 2026.open
Risks flagged
Execution risk remains for Phase 3 trial enrollment and eventual approval.
“Company intends to file the Phase 3 protocol in Q3 2026 and is actively exploring strategic and financial partnership opportunities” · word for word
15 May 202610-QNAVIGATE trial results: missed primary endpoint in ITT but showed statistically significant reduction in varices in per-protocol and US subgroups; FDA Type C meeting granted for Q2 2026.open
Figures in the filing · each found in the filing text
| Research and development expense · Q1-2026 | $2M | -66% y/y |
| General and administrative expense · Q1-2026 | $2M | +31% y/y |
| Cash and cash equivalents · Q1-2026 | $14M | |
| Net cash used in operations · Q1-2026 | $-4M | -50% y/y |
Risks flagged
Clinical trial failure risk
“In the intent-to-treat (ITT) population (N=355), while the incidence of varices was 43.2% reduced ... the composite endpoint did not reach statistical significance.” · word for word
Dependence on financing from chairman
“our dependence on Mr. Uihlein for financing” · word for word
No approved products / revenue
“we have incurred significant operating losses since our inception and cannot assure you that we will generate revenue or profit” · word for word
Regulatory uncertainty
“we are subject to extensive and costly regulation by the U.S. Food and Drug Administration (FDA)” · word for word
15 May 20268-K · 2.02Galectin Therapeutics reports Q1 2026 financials and provides belapectin program update. Additional NAVIGATE trial analyses show statistically significant reductions in liver stiffness (FibroScan) for belapectin 2 mg/kg arm vs placebo. Upcoopen
Figures in the filing · each found in the filing text
| Cash and cash equivalents · Q1-2026 | $14M | |
| Research and development expenses · Q1-2026 | $2M | -66% y/y |
| General and administrative expenses · Q1-2026 | $2M | +29% y/y |
| Net loss applicable to common stockholders · Q1-2026 | $-5M | -47% y/y |
| Net loss per share · Q1-2026 | $-0.08 | |
| Credit line available · Q1-2026 | $10M |
Risks flagged
Belapectin still in clinical development; no approved product or revenue. Regulatory and commercial uncertainty remains high.
“No revenue-generating products; cash burn continues; FDA meeting outcome uncertain.”
Cash runway only through May 2027; may require additional financing if development timeline extends.
“The Company believes it has sufficient cash to fund currently planned operations and research and development activities through May 2027.” · word for word
31 Mar 20268-K · 2.02Galectin Therapeutics reported FY2025 financial results with cash $17.7M and $10M line of credit. Belapectin NAVIGATE trial data shows reduced varices incidence in MASH cirrhosis. Upcoming FDA meeting in Q2 2026. Cash runway extended througearningsopen
Figures in the filing · each found in the filing text
| Unrestricted cash and cash equivalents · FY2025 | $18M | |
| Line of credit available · FY2025 | $10M |
Risks flagged
Clinical and regulatory risks for belapectin in MASH cirrhosis; NAVIGATE trial did not meet primary endpoint with statistical significance
“Composite endpoint did not reach statistical significance in ITT population; per-protocol results nominal p=0.04.”
Cash burn risk with limited revenue; reliance on line of credit and potential financing
“Cash $17.7M plus $10M line of credit; no approved products generating revenue.”
31 Mar 202610-KAnnual results show continued net losses, no revenue, and clinical trial failure; going concern risk persists.earningsopen
Figures in the filing · each found in the filing text
| Net loss · FY2025 | $-30M | |
| Cash used in operations · FY2025 | $-24M | |
| Accumulated deficit · FY2025 | $431M | |
| Cash and cash equivalents · FY2025 | $18M | |
| Research and development expense · FY2025 | $14M | -61% y/y |
| General and administrative expense · FY2025 | $6M | -1% y/y |
Risks flagged
Going concern risk
“We have from time to time faced substantial doubt about our ability to continue as a going concern.” · word for word
Financing dependency on single individual
“We are significantly dependent on Mr. Uihlein for financing, and there is no assurance that he will continue to provide funding.” · word for word
Clinical trial failure
“The composite endpoint did not reach statistical significance.” · word for word
14 Nov 202510-QNAVIGATE trial results: missed primary endpoint in ITT but showed statistical significance in per-protocol and US subgroups.open
Figures in the filing · each found in the filing text
| Cash and cash equivalents · 2025-09-30 | $12M | |
| Net cash used in operations · 9M-2025 | $18M | -39% y/y |
Risks flagged
Clinical trial failure risk
“In the intent-to-treat (ITT) population (N=355), while the incidence of varices was 43.2% reduced in the belapectin 2 mg/kg dose group vs placebo, the composite endpoint did not reach statistical significance.” · word for word
Dependence on future financing
“We will require more cash to fund our operations after June 30, 2026. There can be no assurance that we will be successful in obtaining such new financing” · word for word
14 Nov 20258-K · 2.02Galectin Therapeutics reports positive 18-month biomarker data from NAVIGATE trial for belapectin in MASH cirrhosis, showing consistent antifibrotic activity and reduced portal hypertension risk.open
Risks flagged
Regulatory and clinical development risks remain; FDA feedback on next steps is pending.
“We submitted the NAVIGATE data package to the FDA and requested feedback on proposed next steps, with guidance anticipated by year-end.” · word for word
GALECTIN THERAPEUTICS INC — questions
- What did GALECTIN THERAPEUTICS INC file recently?
- 13 SEC filings in the last 12 months. Latest: DEF 14A on 2026-10-13 — Proxy statement for 2026 annual meeting, including proposals to increase authorized shares and equity plan shares, and disclosure of Chairman's debt-to-equity conversion.
Every figure on this page comes from GALECTIN THERAPEUTICS INC's own SEC filings — see them on SEC EDGAR. Price data is licensed and shown only inside the product.
How these figures are read: methodology · EquiReason.