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GALT Overview

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ET
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Intellectia

Loading chart...

High
4.660
Open
4.600
VWAP
4.53
Vol
437.23K
Mkt Cap
303.60M
Low
4.310
Amount
1.98M
EV/EBITDA(TTM)
--
Total Shares
65.86M
EV
428.72M
EV/OCF(TTM)
--
P/S(TTM)
--
Galectin Therapeutics, Inc. is a clinical-stage biopharmaceutical company dedicated to developing therapies to improve the lives of patients with chronic liver disease and cancer. The Company’s drug candidates are based on its method of targeting galectin proteins, which are key mediators of biologic and pathologic functions. The Company’s lead drug, belapectin, is a carbohydrate-based drug that inhibits the galectin-3 protein, which is directly involved in multiple inflammatory, fibrotic, and malignant diseases for which it has Fast Track designation by the U.S. Food and Drug Administration. The lead development program is in metabolic dysfunction-associated steatohepatitis (MASH, formerly known as nonalcoholic steatohepatitis, or NASH) with cirrhosis, the most advanced form of MASH-related fibrosis. The Company's additional development programs are in the treatment of combination immunotherapy for advanced head and neck cancers and other malignancies.
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Events Timeline

(ET)
2026-06-23
08:31:00
Galectin Therapeutics FDA Meeting Supports Belapectin for MASH Cirrhosis
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2026-05-27 (ET)
2026-05-27
09:20:00
Galectin Therapeutics Presents New Analyses of Belapectin at EASL 2026
select
2026-05-11 (ET)
2026-05-11
09:30:00
Galectin Therapeutics Publishes Belapectin Clinical Trial Results
select
2026-03-31 (ET)
2026-03-31
16:20:00
Galectin Therapeutics Files $200M Mixed Securities Shelf
select
2026-03-17 (ET)
2026-03-17
08:20:00
Galectin Therapeutics Appoints Henry Brem as Independent Director
select
2025-12-19 (ET)
2025-12-19
08:10:00
Galectin Therapeutics Receives FDA Written Response on Belapectin Development Program
select
2025-11-14 (ET)
2025-11-14
08:08:15
Galectin Therapeutics announces Q4 earnings per share of 13 cents, compared to a loss of 18 cents last year.
select
2025-11-10 (ET)
2025-11-10
08:25:07
Galectin Therapeutics showcases NAVIGATE trial findings at AASLD
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2025-08-18 (ET)
2025-08-18
08:45:02
Significant Borrowing Rate Hikes Among Liquid Assets
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News

NASDAQ.COM
7.5
06-25NASDAQ.COM
Pulsenmore Soars 280% on Ouma Health Collaboration
  • Strategic Partnership: Pulsenmore Ltd. has entered into a collaboration with Ouma Health, a provider of virtual maternity care solutions in the U.S., enabling the integration of its FDA-authorized home ultrasound platform, which is expected to significantly enhance customer satisfaction and strengthen market competitiveness.
  • Stock Surge: Following the announcement of the partnership, Pulsenmore's stock soared by as much as 280%, closing up 93.26%, reflecting strong market confidence in its future growth potential.
  • Technological Innovation: By introducing ultrasound monitoring into homes, Pulsenmore not only increases the frequency of contact between expectant mothers and their care teams but also potentially drives the adoption of virtual healthcare services, aligning with the industry's shift towards digital transformation.
  • Market Outlook: This collaboration marks a significant positioning for Pulsenmore in the rapidly growing virtual healthcare market, likely attracting more investor attention and enhancing its standing within the industry.
NASDAQ.COM
8.5
06-24NASDAQ.COM
Boundless Bio Merges with Serapha in All-Stock Deal
  • Merger Overview: Boundless Bio has agreed to merge with privately held Serapha Bio in an all-stock transaction expected to close in Q4 2026, with the combined entity to operate under the name Serapha Bio, Inc. and trade on Nasdaq as "AATD", enhancing its competitive position in the biopharmaceutical market.
  • Cash Dividend Plan: Prior to the merger's completion, Boundless Bio plans to declare a cash dividend to existing shareholders, aimed at boosting shareholder confidence and laying a solid foundation for the upcoming merger, which is expected to attract more investor interest.
  • Clinical Candidate Development: Serapha's lead clinical candidate, SERP-01, is being developed for severe Alpha-1 Antitrypsin Deficiency, which is anticipated to provide new revenue streams for the company and strengthen its market position in the therapeutic area.
  • Stock Performance: Boundless Bio's stock surged 85.71% to close at $2.60, reflecting a positive market reaction to the merger news and indicating investor optimism regarding future growth potential.
stocktwits
8.5
06-23stocktwits
Galectin Therapeutics Reaches Agreement with FDA for Late-Stage Trial
  • FDA Agreement: Galectin Therapeutics has reached an agreement with the U.S. FDA to conduct a late-stage trial for belapectin in patients with MASH cirrhosis and portal hypertension, which is expected to provide a clearer roadmap for potential marketing approval, contributing to a 22% stock price increase on Tuesday.
  • Trial Design: The trial will evaluate a single 2 mg dose of belapectin, aiming to prevent esophageal varices, using the same centralized, blinded endoscopy review process as in a previous trial, with a similar expected size, and plans to submit the final protocol to the FDA in Q3 2026.
  • Market Sentiment Shift: Over the past 24 hours, retail sentiment around GALT shifted from 'bearish' to 'bullish', with message volume rising from 'normal' to 'high', indicating investor optimism regarding an upcoming partnership announcement and the market potential of belapectin.
  • Strategic Partnership Exploration: CEO Joel Lewis noted that the agreement provides “important clarity” and renewed confidence, as Galectin actively seeks strategic partnerships to support the development of belapectin, although approval will follow the traditional full-approval pathway.
NASDAQ.COM
9.0
06-23NASDAQ.COM
Galectin Aligns with FDA on Belapectin Regulatory Path for MASH Cirrhosis
  • FDA Meeting Outcome: Galectin Therapeutics achieved alignment with the U.S. FDA during a recent in-person Type C meeting, clarifying the primary endpoint and regulatory path for Belapectin in Metabolic Dysfunction-Associated Steatohepatitis (MASH) cirrhosis and portal hypertension, marking a significant advancement in the company's clinical development.
  • Phase 3 Trial Plans: The company intends to submit the Phase 3 protocol in Q3 2026, conducting a randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of Belapectin in preventing disease progression in patients with MASH cirrhosis and portal hypertension, indicating potential benefits for patients.
  • Clinical Endpoint Alignment: The FDA and Galectin agreed on a composite clinical endpoint that includes prevention of disease progression and the development of large esophageal varices greater than 5 mm, which is a meaningful indicator of worsening portal hypertension and MASH cirrhosis.
  • Dose Evaluation Plan: Based on efficacy observed in prior clinical studies, the company plans to evaluate a single 2mg dose of Belapectin in the Phase 3 trial, aiming to advance clinical progress and attract strategic and financial partnership opportunities.
seekingalpha
9.0
06-23seekingalpha
Galectin Reaches Agreement with FDA on Phase 3 Trial for Belapectin
  • FDA Agreement: Galectin Therapeutics announced an agreement with the FDA to conduct a Phase 3 trial testing its lead asset belapectin for cirrhosis and portal hypertension linked to metabolic dysfunction-associated steatohepatitis, marking a significant advancement in drug development.
  • Trial Design Confirmation: The FDA has agreed to key components of the Phase 3 program, including its design and primary endpoint, paving the way for potential full approval of belapectin, despite the previous Phase 2b/3 trial failing to meet its primary endpoint.
  • Negative Market Reaction: Despite the agreement, Galectin's shares fell approximately 9% in premarket trading, reflecting market concerns regarding the company's future clinical trial outcomes, which could impact investor confidence.
  • Future Plans: The company expects the planned study to be comparable in size to the NAVIGATE trial, targeting similar patient types, with the final Phase 3 protocol submission anticipated in Q3 2026, demonstrating the company's ongoing commitment to future research.
Newsfilter
8.5
06-23Newsfilter
Galectin Reaches Key Agreement with FDA on Belapectin Approval Path
  • FDA Agreement: Galectin has reached an agreement with the FDA on the primary endpoint and regulatory pathway for belapectin, marking a significant advancement in the treatment of metabolic dysfunction-associated steatohepatitis (MASH) cirrhosis, which is expected to enhance its market competitiveness.
  • Phase 3 Trial Plans: The company intends to submit the Phase 3 protocol in Q3 2026 to assess the safety and efficacy of belapectin in preventing disease progression in MASH cirrhosis patients, demonstrating a commitment to addressing substantial unmet medical needs.
  • Clinical Assessment Methodology: The FDA accepted the company's proposed blinded central endoscopy review process, ensuring standardized and consistent assessment of esophageal varices across global studies, thereby enhancing the scientific rigor of the clinical trial.
  • Strategic Partnership Opportunities: Galectin is actively exploring strategic and financial partnerships to support the continued development and commercialization of belapectin, reflecting the company's confidence in future growth and focus on patient needs.
Wall Street analysts forecast GALT stock price to rise
1 Analyst Rating
Wall Street analysts forecast GALT stock price to rise
1 Buy
0 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
11.00
Averages
11.00
High
11.00
Current: 0.000
sliders
Low
11.00
Averages
11.00
High
11.00
H.C. Wainwright
Matthew Keller
Buy
maintain
$6 -> $11
AI Analysis
2025-12-17
Reason
H.C. Wainwright
Matthew Keller
Price Target
$6 -> $11
AI Analysis
2025-12-17
maintain
Buy
Reason
H.C. Wainwright analyst Matthew Keller raised the firm's price target on Galectin Therapeutics to $11 from $6 and keeps a Buy rating on the shares. The firm says recent biomarker data continue to strengthen confidence in Galectin's metabolic dysfunction-associated steatohepatitis program.

Valuation Metrics

The current forward P/E ratio for Galectin Therapeutics Inc (GALT.O) is 4.54, compared to its 5-year average forward P/E of -2.66. For a more detailed relative valuation and DCF analysis to assess Galectin Therapeutics Inc's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
-2.66
Current PE
4.54
Overvalued PE
0.91
Undervalued PE
-6.23

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
0.00
Current EV/EBITDA
0.00
Overvalued EV/EBITDA
0.00
Undervalued EV/EBITDA
0.00

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PS
1.16
Current PS
0.00
Overvalued PS
6.00
Undervalued PS
-3.67

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Frequently Asked Questions

What is Galectin Therapeutics Inc (GALT) stock price today?

The current price of GALT is 4.61 USD — it has decreased -0.43

What is Galectin Therapeutics Inc (GALT)'s business?

Galectin Therapeutics, Inc. is a clinical-stage biopharmaceutical company dedicated to developing therapies to improve the lives of patients with chronic liver disease and cancer. The Company’s drug candidates are based on its method of targeting galectin proteins, which are key mediators of biologic and pathologic functions. The Company’s lead drug, belapectin, is a carbohydrate-based drug that inhibits the galectin-3 protein, which is directly involved in multiple inflammatory, fibrotic, and malignant diseases for which it has Fast Track designation by the U.S. Food and Drug Administration. The lead development program is in metabolic dysfunction-associated steatohepatitis (MASH, formerly known as nonalcoholic steatohepatitis, or NASH) with cirrhosis, the most advanced form of MASH-related fibrosis. The Company's additional development programs are in the treatment of combination immunotherapy for advanced head and neck cancers and other malignancies.

What is the price predicton of GALT Stock?

Wall Street analysts forecast GALT stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for GALT is11.00 USD with a low forecast of 11.00 USD and a high forecast of 11.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is Galectin Therapeutics Inc (GALT)'s revenue for the last quarter?

Galectin Therapeutics Inc revenue for the last quarter amounts to -4.08M USD, decreased -48.37

What is Galectin Therapeutics Inc (GALT)'s earnings per share (EPS) for the last quarter?

Galectin Therapeutics Inc. EPS for the last quarter amounts to USD, decreased

How many employees does Galectin Therapeutics Inc (GALT). have?

Galectin Therapeutics Inc (GALT) has 9 emplpoyees as of July 08 2026.

What is Galectin Therapeutics Inc (GALT) market cap?

Today GALT has the market capitalization of 303.60M USD.