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Galmed Pharmaceuticals

Full company profile

uuid0003p68

Namestring
Galmed Pharmaceuticals
Legal namestring
Galmed Research & Development Ltd.
Company typeenum
Public
Founded yearint
2000
Descriptiontext

Galmed Pharmaceuticals is an Israeli clinical-stage biopharmaceutical company founded in 2000 by Tuvia Gilat and Allen Baharaff, listed on NASDAQ under the ticker GLMD, and focused on developing therapies for metabolic, inflammatory, and gastrointestinal diseases. Its lead asset is Aramchol, an oral small-molecule inhibitor of stearoyl-CoA desaturase 1 (SCD1), which is being evaluated in the ARMOR Phase 3 study for NASH/MASH and is being reformulated as a meglumine salt to reduce COGS by approximately 50% and improve manufacturing yield. The company is also developing new formulations, including an LNP cardiac-targeted version and an oral-disintegrating-film brain-penetrating version, expanding into cardiac fibrosis, Parkinson's disease, ulcerative colitis, and GI oncology, and has filed a patent covering co-administration of Aramchol with resmetirom (Madrigal's Rezdiffra).

In June 2026, Galmed diversified beyond pure pharma by acquiring Colospan and its CG-100 intraluminal colorectal anastomosis device for approximately $4.5 million; CG-100 carries FDA Breakthrough Device Designation, has CE marking, and is being commercially launched in the DACH region (Germany, Austria, Switzerland), giving Galmed its first revenue-generating product. The company partners with Barcode Nanotech for AI-enabled nanoparticle engineering and with Tissue Dynamics for cardiac organoid testing with embedded metabolic sensors, and has adopted a digital-asset treasury strategy to manage its approximately $19.2M cash position as of Q3 2025. With 11-50 employees, a market capitalization of roughly $3-4M, and ongoing reliance on equity-line and ATM issuance (~$9.3M raised in 2025), Galmed remains thinly capitalized relative to its expanded pipeline and is reliant on continued equity issuance, strategic transactions, or non-dilutive capital to fund ARMOR and the device launch.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersTel Aviv, Israel
HQ citystring
Tel Aviv
HQ countrystring
Israel
HQ regionstring
Middle East
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
clinical-stage biopharmaceutical, NASH/MASH therapeutics, SCD1 inhibitor development, fibrosis drug pipeline, intr luminal bypass device
Industry2 codes
1Gastroenterology Specialty Pharmaceuticals
CodeHLAIACAEPrimaryYes
2Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity)
CodeHLAIAAAEPrimaryNo
NAICS code3 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Scientific Research and Development Services5417
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Surgical & Medical Instruments & Apparatus3841
Product category
Clinical-stage Biopharmaceuticals
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model3 records
1Aramchol (NASH/MASH)
TypeOne Time License
Description

Pre-commercial clinical-stage drug. Aramchol Meglumine is in Phase 3 (ARMOR study) for NASH and fibrosis. Potential future revenue from pharmaceutical product sales upon regulatory approval.

prnewswire.com
2CG-100 Intraluminal Bypass Device
TypeHardware Sales
Description

Commercial-stage medical device acquired via Colospan acquisition. CE marked in EU and approved in Israel. FDA Breakthrough Device Designation with active U.S. pivotal IDE trial. European commercial launch planned for H2 2026 in Germany, Austria, Switzerland ($6M investment).

in.investing.com
3Digital Asset Strategy
TypeData Monetisation
Description

In August 2025, Galmed adopted a digital asset management strategy including potential allocation of up to 50% of its ~$10M cash reserves to digital assets, with a Crypto Committee and Tectona Ltd. advisory engagement.

prnewswire.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Technology or R&D, Operations, Marketing or Sales, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Galmed Pharmaceuticals is a clinical-stage biopharmaceutical company that develops Aramchol, a first-in-class Stearoyl-CoA desaturase 1 (SCD1) inhibitor, in multiple formulations (Meglumine, ODF, LNP cardiac-targeted) for fibrotic and metabolic diseases including NASH/MASH, liver fibrosis, Parkinson's disease, cardiac fibrosis, and GI oncology. The company also markets the CG-100 intraluminal bypass device for colorectal surgery acquired through the acquisition of Colspa Ltd., and develops the MyBiotics microbiome-based therapeutic program.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • 5-fold greater bioavailability with Aramchol Meglumine 400mg once daily vs. Aramchol free acid 300mg twice daily
+5 more records
Product overview1 text field

Galmed Pharmaceuticals is a clinical-stage biopharmaceutical company developing Aramchol, a first-in-class SCD1 inhibitor, across multiple formulations and indications. The core product Aramchol Meglumine targets NASH and fibrosis in Phase 3, while additional formulations include Aramchol ODF for Parkinson's disease and LNP cardiac-targeted formulation for cardiac fibrosis. The Amilo-5MER peptide targets ulcerative colitis, and the MyBiotics program addresses gut microbiome in NASH. Through the Colospan acquisition, Galmed added the CG-100 intraluminal bypass device to its gastrointestinal medtech portfolio.

Product and service6 records
1Aramchol Meglumine
CategoryClinical-stage pharmaceutical (NASH/MASH)
Description

Oral small-molecule SCD1 inhibitor reformulated as a meglumine salt being developed for the treatment of NASH/MASH with liver fibrosis. It targets the underlying metabolic and fibrotic mechanisms of non-alcoholic steatohepatitis and is intended for adult patients with F2-F3 fibrosis.

2Aramchol ODF (Oral Dissolving Film)
CategoryClinical-stage pharmaceutical (liver disease)
Description

Oral dissolving film formulation of Aramchol that dissolves in the mouth without water, offering improved patient convenience and compliance. Designed as a differentiated formulation for regional licensing and commercialization in Asian markets.

3Aramchol LNP Cardiac-Targeted
CategoryClinical-stage pharmaceutical (cardiac fibrosis)
Description

Lipid nanoparticle formulation of Aramchol engineered for cardiac-targeted delivery, intended to treat cardiac fibrosis by delivering the SCD1 inhibitor directly to cardiac tissue. Designed for patients with heart failure and cardiac fibrotic conditions.

4Amilo-5MER
CategoryPreclinical peptide therapeutic
Description

Peptide therapeutic candidate developed for fibrosis and oncology indications. Represents a distinct chemical entity outside the Aramchol franchise, expanding the company's pipeline into peptide-based therapeutics.

5CG-100 Intraluminal Bypass Device
CategoryCommercial medical device
Description

Commercial-stage single-use intraluminal bypass device used during colorectal surgery to protect the anastomosis site by diverting fecal content, reducing the risk of post-surgical complications including anastomotic leak. Sold to hospitals and surgical centers and used intraoperatively by colorectal surgeons.

6MyBiotics Microbiome Program
CategoryPreclinical microbiome therapeutic
Description

Bacterial-derived microbiome therapeutic program developed using MyBiotics Pharma technology, intended for gut microbiome-related indications including GI oncology and other conditions where the gut microbiome plays a therapeutic role.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-09
Description

Galmed acquired Colospan in a $4.5 million deal ($2.5M cash + $2.0M in Galmed ordinary shares) with earnout capped at $2.0M from Q3 2027. Restructured terms increased cash payment by $800,000 to reduce dilution. Colospan becomes a wholly owned subsidiary as Galmed's GI-focused medtech platform. CG-100 holds CE marking in EU and Israeli approval, with FDA Breakthrough Device Designation.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-05-06
Description

Collaboration to develop a human chronic cardiac fibrosis platform using vascularized, sensor-embedded cardiac organoids to advance Aramchol-based therapeutics. Combines Tissue Dynamics' high-throughput organoid technology with embedded metabolic sensors and AI analysis with Galmed's SCD1 biology expertise. Preclinical results showed 4-fold reduction in fibrotic burden.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-04-14
Description

Research collaboration agreement with Ramot at Tel Aviv University to evaluate brain-penetrating SCD1 inhibitor Aramchol as targeted therapy for metastatic brain cancers. Combines TAU's genomic expertise (Ben-David Lab) and 3D preclinical modeling capabilities (Satchi-Fainaro Lab) to validate Aramchol's efficacy in p53-deficient brain metastases.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2026-04-09
Description

Co-development partnership for lipid nanoparticle (LNP) brain-penetrating formulation of Aramchol using Barcode Nanotech's AI-based nanoparticle screening platform. Also co-developed LNP cardiac-targeted formulation and ODF formulation for improved delivery across multiple therapeutic applications.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-11-26
Description

Joint research collaboration with VCU evaluating Aramchol's effects on gastrointestinal cancer drug resistance. Positive top-line results announced from studies showing Aramchol's effect on overcoming drug resistance in GI cancers. Also supports Phase 1b clinical trials planned for early 2026 for metastatic colorectal cancer, hepatocellular carcinoma, and cholangiocarcinoma patients.

Strategic tierMinorTypeOthersAnnounced on2025-08-28
Description

Advisory services engagement for digital asset management strategy. Galmed adopted a digital asset management strategy including potential allocation of up to 50% of ~$10M cash reserves to digital assets, with a Crypto Committee established and Tectona engaged for advisory services.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Lead FDA-approved MASH player with Rezdiffra (resmetirom). Galmed's own combination patent links Aramchol directly to Rezdiffra, making Madrigal the most directly comparable peer and the de facto standard-of-care benchmark for the ARMOR readout.

TypeDirect peer
Description

Clinical-stage NASH/MASH company developing efruxifermin (FGF21 analog), with pivotal-stage data competing for the same advanced-fibrosis MASH opportunity that ARMOR targets.

TypeDirect peer
Description

Pegozafermin (FGF21 analog) developer focused on MASH with advanced fibrosis; directly comparable late-stage clinical-stage peer competing for the same patient population and prescriber demand.

TypeDirect peer
Description

Lanifibranor (pan-PPAR agonist) developer in NASH/MASH Phase 3; European clinical-stage peer with similar regulatory pathway, indication, and market to Galmed's ARMOR program.

TypeDirect peer
Description

Clinical-stage metabolic-disease company with programs in NASH (VK2809) and obesity/CV; comparable because it pursues both liver and broader cardiometabolic indications, mirroring Galmed's NASH + cardiac fibrosis strategy.

TypeDirect peer
Description

Clinical-stage developer of THR-β agonists (e.g., TERN-501) for MASH, positioning as another resmetirom-follower — directly comparable small-cap NASH competitor for capital and partnership attention.

TypeBroad incumbent
Description

Large incumbent with a dedicated NASH/MASH and cardiometabolic pipeline (survodutumab and others in partnership with Zealand Pharma). Broad incumbent across the same liver/cardiac indications Galmed targets.

TypeBroad incumbent
Description

Diversified large-cap pharma with established metabolic (Mounjaro/Zepbound) and active NASH/cardiometabolic programs; sets the broader competitive backdrop against which Galmed's SCD1 platform must differentiate.

TypeBroad incumbent
Description

Owns legacy liver-franchise assets (Hepsera, Viread, Sovaldi) and has publicly pursued NASH candidates. Board member Carol Brosgart led clinical development of Viread and Hepsera at Gilead, illustrating the direct relevance of its hepatic franchise as a comparable.

TypeEmerging player
Description

Private clinical-stage hepatology company advancing FXR agonists (vonafexor) in NASH and chronic HBV; smaller, emerging player addressing the same disease biology and patient population as Galmed's ARMOR program.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment6 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile4 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles9 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance1 record

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds5 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors2 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment1 record

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Galmed Pharmaceuticals

Clinical-stage Biopharmaceuticalsgalmedpharma.com

What Galmed Pharmaceuticals does

Galmed Pharmaceuticals is an Israeli clinical-stage biopharmaceutical company founded in 2000 by Tuvia Gilat and Allen Baharaff, listed on NASDAQ under the ticker GLMD, and focused on developing therapies for metabolic, inflammatory, and gastrointestinal diseases. Its lead asset is Aramchol, an oral small-molecule inhibitor of stearoyl-CoA desaturase 1 (SCD1), which is being evaluated in the ARMOR Phase 3 study for NASH/MASH and is being reformulated as a meglumine salt to reduce COGS by approximately 50% and improve manufacturing yield. The company is also developing new formulations, including an LNP cardiac-targeted version and an oral-disintegrating-film brain-penetrating version, expanding into cardiac fibrosis, Parkinson's disease, ulcerative colitis, and GI oncology, and has filed a patent covering co-administration of Aramchol with resmetirom (Madrigal's Rezdiffra).

In June 2026, Galmed diversified beyond pure pharma by acquiring Colospan and its CG-100 intraluminal colorectal anastomosis device for approximately $4.5 million; CG-100 carries FDA Breakthrough Device Designation, has CE marking, and is being commercially launched in the DACH region (Germany, Austria, Switzerland), giving Galmed its first revenue-generating product. The company partners with Barcode Nanotech for AI-enabled nanoparticle engineering and with Tissue Dynamics for cardiac organoid testing with embedded metabolic sensors, and has adopted a digital-asset treasury strategy to manage its approximately $19.2M cash position as of Q3 2025. With 11-50 employees, a market capitalization of roughly $3-4M, and ongoing reliance on equity-line and ATM issuance (~$9.3M raised in 2025), Galmed remains thinly capitalized relative to its expanded pipeline and is reliant on continued equity issuance, strategic transactions, or non-dilutive capital to fund ARMOR and the device launch.

Galmed Pharmaceuticals firmographics

Firmographics
Name
Galmed Pharmaceuticals
Legal name
Galmed Research & Development Ltd.
Website
https://galmedpharma.com
Company type
Public
Founded year
2000
Operating status
Operating
Headcount range
11–50 employees
Ownership category
akta.pro rank

Galmed Pharmaceuticals industry classification

Industry
Product category
Clinical-stage Biopharmaceuticals
NAICS
Pharmaceutical Preparation Manufacturing (325412), Research and Development in Biotechnology (except Nanobiotechnology) (541714), Scientific Research and Development Services (5417)
SIC
Pharmaceutical Preparations (2834), Surgical & Medical Instruments & Apparatus (3841)
akta.pro primary industry
Gastroenterology Specialty Pharmaceuticals (HLAIACAE)
akta.pro secondary industry
Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity) (HLAIAAAE)

Keywords

  • Clinical-stage biopharmaceutical
  • NASH/MASH therapeutics
  • SCD1 inhibitor development
  • Fibrosis drug pipeline
  • Intr luminal bypass device

Where Galmed Pharmaceuticals is headquartered

Location

Headquarters

HQ city
Tel Aviv
HQ country
Israel
HQ region
Middle East

Offices1 record

Markets served

Galmed Pharmaceuticals business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Personnel, Technology or R&D, Operations, Marketing or Sales, Supply Chain

Revenue model

  1. Aramchol (NASH/MASH): Pre-commercial clinical-stage drug. Aramchol Meglumine is in Phase 3 (ARMOR study) for NASH and fibrosis. Potential future revenue from pharmaceutical product sales upon regulatory approval.
  2. CG-100 Intraluminal Bypass Device: Commercial-stage medical device acquired via Colospan acquisition. CE marked in EU and approved in Israel. FDA Breakthrough Device Designation with active U.S. pivotal IDE trial. European commercial launch planned for H2 2026 in Germany, Austria, Switzerland ($6M investment).
  3. Digital Asset Strategy: In August 2025, Galmed adopted a digital asset management strategy including potential allocation of up to 50% of its ~$10M cash reserves to digital assets, with a Crypto Committee and Tectona Ltd. advisory engagement.

Go-to-market motion1 record

Distribution channels3 records

Marketing channels5 records

Galmed Pharmaceuticals product offering

Product offering

Core offering

Galmed Pharmaceuticals is a clinical-stage biopharmaceutical company that develops Aramchol, a first-in-class Stearoyl-CoA desaturase 1 (SCD1) inhibitor, in multiple formulations (Meglumine, ODF, LNP cardiac-targeted) for fibrotic and metabolic diseases including NASH/MASH, liver fibrosis, Parkinson's disease, cardiac fibrosis, and GI oncology. The company also markets the CG-100 intraluminal bypass device for colorectal surgery acquired through the acquisition of Colspa Ltd., and develops the MyBiotics microbiome-based therapeutic program.

Product overview

Galmed Pharmaceuticals is a clinical-stage biopharmaceutical company developing Aramchol, a first-in-class SCD1 inhibitor, across multiple formulations and indications. The core product Aramchol Meglumine targets NASH and fibrosis in Phase 3, while additional formulations include Aramchol ODF for Parkinson's disease and LNP cardiac-targeted formulation for cardiac fibrosis. The Amilo-5MER peptide targets ulcerative colitis, and the MyBiotics program addresses gut microbiome in NASH. Through the Colospan acquisition, Galmed added the CG-100 intraluminal bypass device to its gastrointestinal medtech portfolio.

Differentiator

Problem solved

Functional benefit

Products and services

  • Aramchol Meglumine Oral small-molecule SCD1 inhibitor reformulated as a meglumine salt being developed for the treatment of NASH/MASH with liver fibrosis. It targets the underlying metabolic and fibrotic mechanisms of non-alcoholic steatohepatitis and is intended for adult patients with F2-F3 fibrosis.
  • Aramchol ODF (Oral Dissolving Film) Oral dissolving film formulation of Aramchol that dissolves in the mouth without water, offering improved patient convenience and compliance. Designed as a differentiated formulation for regional licensing and commercialization in Asian markets.
  • Aramchol LNP Cardiac-Targeted Lipid nanoparticle formulation of Aramchol engineered for cardiac-targeted delivery, intended to treat cardiac fibrosis by delivering the SCD1 inhibitor directly to cardiac tissue. Designed for patients with heart failure and cardiac fibrotic conditions.
  • Amilo-5MER Peptide therapeutic candidate developed for fibrosis and oncology indications. Represents a distinct chemical entity outside the Aramchol franchise, expanding the company's pipeline into peptide-based therapeutics.
  • CG-100 Intraluminal Bypass Device Commercial-stage single-use intraluminal bypass device used during colorectal surgery to protect the anastomosis site by diverting fecal content, reducing the risk of post-surgical complications including anastomotic leak. Sold to hospitals and surgical centers and used intraoperatively by colorectal surgeons.
  • MyBiotics Microbiome Program Bacterial-derived microbiome therapeutic program developed using MyBiotics Pharma technology, intended for gut microbiome-related indications including GI oncology and other conditions where the gut microbiome plays a therapeutic role.

Quantifiable outcome

  • 5-fold greater bioavailability with Aramchol Meglumine 400mg once daily vs. Aramchol free acid 300mg twice daily
  • +5 more outcomes

Companies that use Galmed Pharmaceuticals

Customer profile

Segments6 records

Ideal customer profiles4 records

Galmed Pharmaceuticals technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature6 records

Galmed Pharmaceuticals partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered core and minor.

  • Colospan Ltd.coreStrategic or Co-development Partner · 9 June 2026Galmed acquired Colospan in a $4.5 million deal ($2.5M cash + $2.0M in Galmed ordinary shares) with earnout capped at $2.0M from Q3 2027. Restructured terms increased cash payment by $800,000 to reduce dilution. Colospan becomes a wholly owned subsidiary as Galmed's GI-focused medtech platform. CG-100 holds CE marking in EU and Israeli approval, with FDA Breakthrough Device Designation.
  • Tissue DynamicscoreStrategic or Co-development Partner · 6 May 2026Collaboration to develop a human chronic cardiac fibrosis platform using vascularized, sensor-embedded cardiac organoids to advance Aramchol-based therapeutics. Combines Tissue Dynamics' high-throughput organoid technology with embedded metabolic sensors and AI analysis with Galmed's SCD1 biology expertise. Preclinical results showed 4-fold reduction in fibrotic burden.
  • Tel Aviv University (Ramot)coreStrategic or Co-development Partner · 14 April 2026Research collaboration agreement with Ramot at Tel Aviv University to evaluate brain-penetrating SCD1 inhibitor Aramchol as targeted therapy for metastatic brain cancers. Combines TAU's genomic expertise (Ben-David Lab) and 3D preclinical modeling capabilities (Satchi-Fainaro Lab) to validate Aramchol's efficacy in p53-deficient brain metastases.
  • Barcode NanotechcoreTechnology or Integration · 9 April 2026Co-development partnership for lipid nanoparticle (LNP) brain-penetrating formulation of Aramchol using Barcode Nanotech's AI-based nanoparticle screening platform. Also co-developed LNP cardiac-targeted formulation and ODF formulation for improved delivery across multiple therapeutic applications.
  • Virginia Commonwealth University (VCU) - Massey Comprehensive Cancer CentercoreStrategic or Co-development Partner · 26 November 2025Joint research collaboration with VCU evaluating Aramchol's effects on gastrointestinal cancer drug resistance. Positive top-line results announced from studies showing Aramchol's effect on overcoming drug resistance in GI cancers. Also supports Phase 1b clinical trials planned for early 2026 for metastatic colorectal cancer, hepatocellular carcinoma, and cholangiocarcinoma patients.
  • Tectona Ltd.minorOthers · 28 August 2025Advisory services engagement for digital asset management strategy. Galmed adopted a digital asset management strategy including potential allocation of up to 50% of ~$10M cash reserves to digital assets, with a Crypto Committee established and Tectona engaged for advisory services.

Scale indicators7 records

Recent moves7 records

Expansion highlights6 records

Galmed Pharmaceuticals competitors and assessment

Company assessment

Direct peers

  • Madrigal Pharmaceuticals: Lead FDA-approved MASH player with Rezdiffra (resmetirom). Galmed's own combination patent links Aramchol directly to Rezdiffra, making Madrigal the most directly comparable peer and the de facto standard-of-care benchmark for the ARMOR readout.
  • Akero Therapeutics: Clinical-stage NASH/MASH company developing efruxifermin (FGF21 analog), with pivotal-stage data competing for the same advanced-fibrosis MASH opportunity that ARMOR targets.
  • 89bio: Pegozafermin (FGF21 analog) developer focused on MASH with advanced fibrosis; directly comparable late-stage clinical-stage peer competing for the same patient population and prescriber demand.
  • Inventiva Pharma: Lanifibranor (pan-PPAR agonist) developer in NASH/MASH Phase 3; European clinical-stage peer with similar regulatory pathway, indication, and market to Galmed's ARMOR program.
  • Viking Therapeutics: Clinical-stage metabolic-disease company with programs in NASH (VK2809) and obesity/CV; comparable because it pursues both liver and broader cardiometabolic indications, mirroring Galmed's NASH + cardiac fibrosis strategy.
  • Terns Pharmaceuticals: Clinical-stage developer of THR-β agonists (e.g., TERN-501) for MASH, positioning as another resmetirom-follower — directly comparable small-cap NASH competitor for capital and partnership attention.

Broad incumbents

  • Boehringer Ingelheim: Large incumbent with a dedicated NASH/MASH and cardiometabolic pipeline (survodutumab and others in partnership with Zealand Pharma). Broad incumbent across the same liver/cardiac indications Galmed targets.
  • Eli Lilly: Diversified large-cap pharma with established metabolic (Mounjaro/Zepbound) and active NASH/cardiometabolic programs; sets the broader competitive backdrop against which Galmed's SCD1 platform must differentiate.
  • Gilead Sciences: Owns legacy liver-franchise assets (Hepsera, Viread, Sovaldi) and has publicly pursued NASH candidates. Board member Carol Brosgart led clinical development of Viread and Hepsera at Gilead, illustrating the direct relevance of its hepatic franchise as a comparable.

Emerging players

  • Enyo Pharma: Private clinical-stage hepatology company advancing FXR agonists (vonafexor) in NASH and chronic HBV; smaller, emerging player addressing the same disease biology and patient population as Galmed's ARMOR program.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights6 records

Customer concentration

Galmed Pharmaceuticals social profiles

Digital presence

Galmed Pharmaceuticals compliance and trust

Trust signal

Compliance1 record

Galmed Pharmaceuticals financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Galmed Pharmaceuticals leadership team

Management profile

Number of profiles

Profiles9 records

Galmed Pharmaceuticals subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Galmed Pharmaceuticals funding detail

Funding detail

Funding overview

Funding rounds5 records

Investors2 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Galmed Pharmaceuticals M&A and investment

M&A and investment

M&A1 record

Investments1 record

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Galmed Pharmaceuticals

What does Galmed Pharmaceuticals do?

Galmed Pharmaceuticals is a clinical-stage biopharmaceutical company that develops Aramchol, a first-in-class Stearoyl-CoA desaturase 1 (SCD1) inhibitor, in multiple formulations (Meglumine, ODF, LNP cardiac-targeted) for fibrotic and metabolic diseases including NASH/MASH, liver fibrosis, Parkinson's disease, cardiac fibrosis, and GI oncology. The company also markets the CG-100 intraluminal bypass device for colorectal surgery acquired through the acquisition of Colspa Ltd., and develops the MyBiotics microbiome-based therapeutic program.

Is Galmed Pharmaceuticals a public or private company?

Galmed Pharmaceuticals is a public company. It is classified as public and is currently operating.

When was Galmed Pharmaceuticals founded?

Galmed Pharmaceuticals was founded in 2000. It employs 11 to 50 people.

Where is Galmed Pharmaceuticals based?

Galmed Pharmaceuticals is headquartered in Tel Aviv, Israel, in the Middle East region.

How does Galmed Pharmaceuticals make money?

Three revenue lines are on record. Aramchol (NASH/MASH) is the primary driver. The others are CG-100 Intraluminal Bypass Device and digital Asset Strategy.

Who are Galmed Pharmaceuticals's main competitors?

Direct peers on record are Madrigal Pharmaceuticals, Akero Therapeutics, 89bio, Inventiva Pharma, Viking Therapeutics and Terns Pharmaceuticals. Broad incumbents are Boehringer Ingelheim, Eli Lilly and Gilead Sciences. Enyo Pharma is listed as an emerging player.

Does Galmed Pharmaceuticals have an API?

No public API is recorded for Galmed Pharmaceuticals.

What industry is Galmed Pharmaceuticals in?

Galmed Pharmaceuticals's product category is Clinical-stage Biopharmaceuticals. Its primary akta.pro industry code is HLAIACAE, Gastroenterology Specialty Pharmaceuticals, with a secondary code of HLAIAAAE, Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity). Its NAICS code is 325412 and its SIC code is 2834.

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Markets DailyGalmed Pharmaceuticals (NASDAQ:GLMD) Stock Price Crosses Above 50-Day Moving Average – What’s Next?Galmed Pharmaceuticals' stock crossed above its 50-day moving average on Thursday, trading at $4.59. Analysts have an average 'Sell' rating, and the company reported Q2 EPS of -$2.86, beating the -$3.12 consensus.American Banking and Market NewsGalmed Pharmaceuticals (NASDAQ:GLMD) Shares Break Above Fifty Day Moving Average – What’s Next?Galmed Pharmaceuticals shares traded above their 50-day moving average on Thursday, reaching $4.63 from a $4.59 close. Weiss Ratings reiterated a sell rating, and the company's consensus rating is Sell. The stock's Q2 EPS of -$2.86 beat the -$3.12 consensus.American Banking and Market NewsGalmed Pharmaceuticals (NASDAQ:GLMD) Share Price Breaks Above 50-Day Moving Average – Time to Sell?Galmed Pharmaceuticals shares crossed above its 50-day moving average on Wednesday, trading at $4.59. Weiss Ratings reaffirmed a sell rating, and the stock has a consensus sell rating. The company reported Q2 EPS of -$2.86, beating the consensus of -$3.12.YahooGalmed Pharmaceuticals Becomes EoCene, Unveiling New Ticker Symbol "EOCN" to Reflect its New Dawn Platform for GI InnovationGalmed Pharmaceuticals rebranded to Eocene Ltd. and changed its Nasdaq ticker to EOCN, effective September 10, 2026. The new name reflects its GI-focused platform, integrating Colospan's medical device technology for colorectal surgery complications.Stock TitanGalmed Plans EoCene Name, EOCN Ticker ChangeGalmed Pharmaceuticals rebranded to EoCene and changed its Nasdaq ticker to EOCN, effective September 10, 2026. The company also terminated its $20 million standby equity line with Yorkville, having raised about $7.3 million. The rebrand reflects its shift to a GI-focused biopharmaceutical and medical device platform after acquiring Colospan.PR NewswireGalmed Pharmaceuticals Becomes EoCene, Unveiling New Ticker Symbol "EOCN" to Reflect its New Dawn Platform for GI InnovationGalmed Pharmaceuticals rebranded to EoCene, changing its Nasdaq ticker to EOCN, effective September 10, 2026. The company also terminated its $20 million standby equity purchase agreement with Yorkville, having raised about $7.3 million. The rebranding reflects its shift to a GI-focused biopharmaceutical and medical device platform.Ticker ReportGalmed Pharmaceuticals Ltd. (NASDAQ:GLMD) Short Interest Down 74.7% in AugustGalmed Pharmaceuticals' short interest fell 74.7% to 37,252 shares as of August 14, down from 146,971 in late July, with about 4.5% of shares short sold and a 0.9-day-to-cover ratio. The stock closed at $4.16, down $0.15, with a market cap of $4.33 million and a "Sell" consensus rating. Two Sigma Investments bought 21,200 shares in the third quarter.AijournGalmed Announces Successful First-in-Human Proof-of-Concept Clinical Study Results for Colospan’s Novel Intraoperative Tissue Assessment TechnologyColospan Ltd., a subsidiary of Galmed Pharmaceuticals Ltd., successfully completed a feasibility study involving 32 colorectal cancer patients at three clinical centers in Israel, demonstrating the viability of a novel intraoperative tissue assessment technology. This technology aims to provide real-time, objective measurements of colon tissue quality during surgeries, potentially aiding in surgical decision-making and improving patient outcomes. The study reinforces Galmed's strategy to innovate in GI oncology and colorectal surgery, expanding Colospan's product pipeline.Investing.comGalmed completes feasibility study for colon tissue assessment tech By Investing.comGalmed Pharmaceuticals completed a feasibility study for a colon tissue assessment platform through its subsidiary Colospan Ltd., demonstrating that quantitative measurement of colon tissue compliance is feasible in 32 colorectal cancer patients. The technology aims to provide surgeons with real-time data on tissue mechanical properties to support intraoperative decision-making during colorectal surgery. This development complements Colospan's existing CG-100 device, which has received FDA Breakthrough Device Designation.PR NewswireGalmed Announces Successful First-in-Human Proof-of-Concept Clinical Study Results for Colospan's Novel Intraoperative Tissue Assessment TechnologyGalmed Pharmaceuticals announced the successful completion of a first-in-human feasibility study for Colospan's novel intraoperative tissue assessment technology, which demonstrated technical feasibility in measuring colon tissue quality across 32 colorectal cancer patients. This development establishes a clinical foundation for a second product platform that complements Colospan's existing CG-100 device and supports Galmed's strategy to diversify its portfolio in colorectal surgery. The results indicate no measurement failures, paving the way for future clinical trials and regulatory submissions.