EOCNNasdaqPharmaceutical PreparationsUS GAAP · USD

Galmed Pharmaceuticals Ltd.

Galmed Pharmaceuticals Ltd. is a biopharmaceutical company focused on developing Aramchol, a synthetic fatty acid-bile acid conjugate, for liver disease and oncology-related indications. The company is incorporated in Israel and operates through subsidiaries in Israel, Malta, and the United Kingdom, with its securities listed in the United States.

Nettotulos−10,3milj. USD
−37,1 %v/v

Tilikausi 2025 · muutos edellisvuodesta

Kehitys 2020–2025

−40−30−20−100milj. USD2020: 0,00 milj. USD2020: EBIT −30 milj. USD202020212022202320242025
LiikevaihtoLiikevoitto (EBIT)
Kysy Clarifolta: Galmed Pharmaceuticals Ltd.

Liiketoiminta

Osuus liikevaihdosta
Lead drug candidate development70 %

Development of Aramchol as a therapeutic candidate for liver disease and oncology indications.

GI-focused oncology pipeline20 %

Research and development programs targeting gastrointestinal and GI-related oncology uses.

Platform and IP assets10 %

Intellectual property, licensing, and development capabilities supporting future programs.

Asiakkaat

Galmed is primarily a development-stage biopharmaceutical company, so its direct “customers” are not end patients but rather future pharmaceutical partners, licensees, and potential commercial collaborators. Its programs are designed for healthcare providers and patients in liver disease, gastrointestinal disease, and oncology settings once a product reaches commercialization.

Pharma licensing partners

Buy or license clinical-stage assets such as Aramchol to expand their therapeutic pipelines.

Future healthcare providers

Would prescribe or administer Galmed’s therapies if approved for liver or GI oncology indications.

Future patients

Patients with liver disease or GI-related cancers who are the eventual end users of approved drugs.

Research and development collaborators

Partners that support development programs, data generation, or clinical advancement.

Strategia

Galmed’s strategy centers on advancing Aramchol through development for GI and oncology indications and positioning the company as a specialty GI biopharmaceutical platform. The company also appears to be building capability through complementary transactions and partnerships that expand its therapeutic scope and potential commercialization options.

Advance Aramchol through clinical developmentLyhyt aikaväli

Clinical progress is the main value driver for a development-stage biopharmaceutical company.

Broaden into GI-related oncologyKeskipitkä aikaväli

A wider indication set can enlarge the addressable market and diversify pipeline risk.

Develop a specialty GI platformKeskipitkä aikaväli

A focused therapeutic platform can improve partnering leverage and strategic differentiation.

Maantiede

Galmed is incorporated in Israel and maintains subsidiaries in Malta, Israel, and the United Kingdom, while its securities trade in the United States. Its business footprint is therefore international even though the core operating and development structure is centered in Israel and adjacent jurisdictions.

Riskit

Galmed faces the classic risks of a development-stage biotech company: clinical failure, regulatory setbacks, and the need to fund long development cycles before commercialization. The company also carries acquisition integration, IP, and going-concern style funding risk, which are especially important because its value depends on advancing a small number of programs successfully.

Järjestetty vakavuuden mukaan
MatalaKohtalainenKorkeaMatalaKohtalainenKorkeaVaikutus →Todennäköisyys →Clinical development failure1Regulatory approval risk3Capital funding risk2Intellectual property litigation4Integration risk from acquisitions5
Vaikutus on riskin vakavuus ja todennäköisyys sen toteutumisen todennäköisyys lähivuosina, molemmat arvioitu yhtiön raporttien perusteella. Numerot vastaavat listaa.
  1. Clinical development failureVaikutus: KriittinenTodennäköisyys: Kohtalainen

    Aramchol is still under evaluation, so negative trial results could materially reduce pipeline value.

    Kohdistuu: Lead asset Aramchol

  2. Capital funding riskVaikutus: KorkeaTodennäköisyys: Korkea

    The company states it will need substantial additional capital to fund operations and development.

    Kohdistuu: Operations and R&D funding

  3. Regulatory approval riskVaikutus: KorkeaTodennäköisyys: Kohtalainen

    Drug candidates must clear safety and efficacy hurdles before commercialization.

    Kohdistuu: Liver disease and oncology indications

  4. Intellectual property litigationVaikutus: KeskitasoTodennäköisyys: Kohtalainen

    The reports reference infringement, damages, royalties, and legal defense costs.

    Kohdistuu: Patent and IP disputes

  5. Integration risk from acquisitionsVaikutus: KeskitasoTodennäköisyys: Kohtalainen

    Acquired assets and businesses must be integrated without disrupting development plans.

    Kohdistuu: Colospan-related transaction

Kirjanpito

Harkinnanvaraiset erät
Research and development expense recognition

Most development costs are expensed as incurred, which makes earnings highly sensitive to pipeline activity.

Vaikutus: Directly affects operating loss and quarterly comparability

Going-concern assessment

The company discloses that continuation depends on future capital resources and operating plans.

Vaikutus: Important for evaluating balance sheet and financing risk

Pro forma acquisition accounting

The Colospan transaction includes revised unaudited pro forma financial statements.

Vaikutus: Can change the presentation of assets, liabilities, and future earnings base

Shares outstanding and diluted EPS

Equity issuance changes the weighted-average share count used in loss per share calculations.

Vaikutus: Affects reported per-share losses

Julkisesti listattuja yhtiöitä, joilla on samankaltainen liiketoiminta.

Päivitetty: 28.9.2026

Galmed Pharmaceuticals Ltd. (Nasdaq) – Pharmaceutical Preparations | Analyysi – Clarifo