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GALTNasdaq

GALECTIN THERAPEUTICS INC

Biopharma developer (SEC filing verified)·Phase 2·Norcross, GA, United States·CEO: Mr. Joel Lewis CPA
OncologyInfectious DiseaseMetabolicGastroenterology

GALT evidence brief

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Prepared research question

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BioSniper AI · GALT

Galectin Therapeutics is a clinical-stage biopharmaceutical company developing therapies for fibrotic disease, cancer, and other conditions based on targeting galectin proteins, with its lead candidate belapectin (GR-MD-02) having completed a Phase 2b/3 trial in NASH cirrhosis that was terminated.

Key risk: Clinical trial failure

2.5/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$405.4M

Cash Runway

16.8 mo

Next Catalyst

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate · 2 clinical trials for GALECTIN THERAPEUTICS INC.

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AI OverviewAI overview is shown in English only.

Galectin Therapeutics is a clinical-stage biopharmaceutical company developing therapies for fibrotic disease, cancer, and other conditions based on targeting galectin proteins, with its lead candidate belapectin (GR-MD-02) having completed a Phase 2b/3 trial in NASH cirrhosis that was terminated.

  • Galectin Therapeutics is a clinical-stage biopharmaceutical company focused on drug research and development for fibrotic disease, cancer, and selected other diseases, using galectin protein targeting [sec_mda · as of 2026-03-31].
  • The company's lead drug candidate, belapectin (GR-MD-02), is a proprietary complex carbohydrate derived from naturally occurring plant products [sec_mda · as of 2026-03-31].
  • A Phase 2b/3 clinical trial (NAVIGATE, NCT04365868) for belapectin in NASH cirrhosis was terminated [catalyst].
  • As of 2026-06-30, the company reported cash and equivalents of $13.3M, a net loss of $9.1M, and negative shareholders' equity of $127.9M [sec].
  • The company faces risks including inability to demonstrate efficacy in human trials, extensive FDA regulation, and limited trading volume [sec_mda · as of 2026-08-14].

What works

  • Belapectin has completed a pharmacokinetic study in subjects with hepatic impairment (NCT04332432), which became fully enrolled in February 2022 and reported favorable results in 2023 [sec_mda · as of 2026-08-14].
  • The company leverages established relationships with outside sources for preclinical models, toxicology, clinical trial operations, and manufacturing to achieve cost-effective drug development [sec_mda · as of 2026-08-14].
  • Galectin's technology uses naturally occurring, readily-available plant products as starting material, which may provide a scalable manufacturing advantage [sec_mda · as of 2026-03-31].

What to weigh

  • The company's Phase 2b/3 NAVIGATE trial for belapectin in NASH cirrhosis was terminated, raising uncertainty about the drug's clinical path [catalyst].
  • As of 2026-06-30, the company had negative shareholders' equity of $127.9M and a net loss of $9.1M, indicating a weak financial position [sec].
  • The company is subject to extensive and costly FDA regulation and may be unable to demonstrate the efficacy and safety of its product candidates in human trials [sec_mda · as of 2026-08-14].
  • Limited trading volume and concentration of stock ownership are noted risks that could affect liquidity and stock price [sec_mda · as of 2026-08-14].

From the filings

Quoted directly from source documents.

  • Galectin is a clinical-stage biopharmaceutical company targeting galectin proteins for fibrotic disease and cancer.

    We are a clinical stage biopharmaceutical company engaged in drug research and development to create new therapies for fibrotic disease, cancer and selected other diseases. Our drug candidates are based on our method of targeting galectin proteins, which are key mediators of biologic and pathologic functions.

    SEC MD&A · March 31, 2026

  • Belapectin is a proprietary complex carbohydrate derived from plant products.

    We use naturally occurring, readily-available plant products as starting material in manufacturing processes to create proprietary, patented complex carbohydrates with specific mole

    SEC MD&A · March 31, 2026

  • The NAVIGATE Phase 2b/3 trial was terminated.

    Phase 3 Topline: A Seamless, Adaptive, Phase 2b/3, Double-Blind, Randomized, Placebo-controlled, Multicenter, Interna - NCT: NCT04365868. Status: Terminated.

    Catalysts

Catalyst timeline

  • 2020-06-16 · Phase 1 Start: A Single-dose, Open-label, Pharmacokinetic Study of Belapectin (GR-MD-02) in Subjects With Normal HeThis study (NCT04332432) was completed and reported favorable results in 2023, but no new catalysts are listed beyond this.
  • 2025-03-31 · Earnings: Earnings Report - SEC 8-K filingThis is a past earnings event; no future catalyst dates are provided.
  • 2025-04-10 · Phase 3 Topline: A Seamless, Adaptive, Phase 2b/3, Double-Blind, Randomized, Placebo-controlled, Multicenter, InternaThis trial (NCT04365868) was terminated, so no future topline results are expected.
Risks & what to watch (4)

Key risks

  • Clinical trial failureThe Phase 2b/3 NAVIGATE trial for belapectin was terminated, casting doubt on the drug's future [catalyst].
  • Negative equity and lossesAs of 2026-06-30, shareholders' equity was -$127.9M and net loss was $9.1M, indicating financial distress [sec].
  • Regulatory and efficacy risksThe company may be unable to demonstrate efficacy in human trials and is subject to extensive FDA regulation [sec_mda · as of 2026-08-14].
  • Low liquidity and ownership concentrationLimited trading volume and concentrated stock ownership are noted risks [sec_mda · as of 2026-08-14].

What to watch

  • Any updates on belapectin's clinical development path following the termination of the NAVIGATE trial [catalyst].
  • The company's ability to raise additional capital given its negative equity and cash burn [sec].
  • Potential strategic partnerships or licensing deals that could provide funding or development support [sec_mda · as of 2026-08-14].
  • Regulatory decisions or feedback from the FDA regarding belapectin's future [sec_mda · as of 2026-08-14].

Sources: Catalysts · SEC MD&A · Generated August 28, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway4.7

16.8 months

Financial Health0.5

OCF -$2M · Net income -$9M

Pipeline Maturity4.0

Lead: Phase 1

Pipeline Breadth3.3

1 candidate

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal0.0

0 buys · 8 sells (180d)

Runway

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

99

Total value held

$45.8M

Showing top 10 of 99 institutional holders of GALECTIN THERAPEUTICS INC. Open the full 13F history after sign-in.

Short Interest

as of May 21, 2026
% of float
17.6%
Days to cover
21.9
Shares short
7,388,749
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

GALT short interest

Governance

Frequently asked questions

What is the AI investment thesis for GALECTIN THERAPEUTICS INC?

Galectin Therapeutics is a clinical-stage biopharmaceutical company developing therapies for fibrotic disease, cancer, and other conditions based on targeting galectin proteins, with its lead candidate belapectin (GR-MD-02) having completed a Phase 2b/3 trial in NASH cirrhosis that was terminated.

What is GALECTIN THERAPEUTICS INC's lead drug candidate?

GALECTIN THERAPEUTICS INC's most advanced tracked candidate is belapectin (Phase 1) for Hepatic Impairment; Prevention of Esophageal Varices.

Who is the CEO of GALECTIN THERAPEUTICS INC?

Mr. Joel Lewis CPA is the chief executive officer of GALECTIN THERAPEUTICS INC (GALT).

Where is GALECTIN THERAPEUTICS INC headquartered?

GALECTIN THERAPEUTICS INC (GALT) is headquartered in Norcross, GA, United States.

What therapeutic areas does GALECTIN THERAPEUTICS INC focus on?

GALECTIN THERAPEUTICS INC develops therapies across Oncology, Infectious Disease, Metabolic, Gastroenterology.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.