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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

GALTGALECTIN THERAPEUTICS INCFollow GALT — free
Drug Manufacturers - General · Healthcare
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Market cap
321.7M
P/E TTM
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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 · SEC

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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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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 · 2026-07-3149.3%

Risks flagged

Concentrated ownership risk

“Richard E. Uihlein holds 49.3% beneficial ownership, giving significant control.”
Read the original on SEC EDGAR ↗
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 · 2026-07-3134,376,167
Total shares outstanding post-conversion · 2026-07-31100,849,644
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
Read the original on SEC EDGAR ↗
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 · 2026-07-3149.3%

Risks flagged

Concentrated ownership risk

“Richard E. Uihlein holds 49.3% beneficial ownership, giving significant control.”
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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.”
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗
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
Read the original on SEC EDGAR ↗

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.