Galmed Pharmaceuticals Announces $1.9 Million Loss in Q3; Showcases Advancements in Pipeline
Financial Performance: Galmed Pharmaceuticals reported a net loss of $1.89 million for Q3 2025, a slight improvement from a loss of $1.91 million in Q3 2024, with increased R&D expenses and decreased administrative costs.
Pipeline Developments: The company is advancing its lead drug candidate, Aramchol Meglumine, for nonalcoholic steatohepatitis (NASH) and fibrosis, which showed promising results in a Phase 2b study and is now in a Phase 3 trial.
New Drug Candidate: Galmed is also developing Amilo-5MER, a peptide targeting chronic inflammation, currently in a Phase 1 trial for safety and tolerability, with potential applications in ulcerative colitis.
Collaborative Efforts: The company is collaborating on the MyBiotics program, which focuses on microbiome modulation for potential treatment of NASH and fibrosis.
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Galmed Pharmaceuticals to Initiate Phase 1/2 Trial of Aramchol and Regorafenib in 2026
- Clinical Trial Launch: Galmed Pharmaceuticals announced the initiation of a Phase 1/2 clinical trial for the combination of Aramchol and Regorafenib in 2026, aimed at enhancing treatment efficacy for hepatocellular carcinoma and other GI cancers, marking a significant advancement in the company's liver disease treatment efforts.
- Scientific Rationale Strengthened: Research indicates that Aramchol significantly enhances Bayer's Regorafenib efficacy in GI cancer models through SCD1 inhibition, providing a solid scientific foundation for the upcoming clinical trial.
- Investor Value Enhancement: Positive outcomes from the clinical trial could lay the groundwork for expanding Galmed's oncology pipeline, potentially attracting more investor interest and increasing the company's overall market value.
- Industry Recognition: The acceptance of Galmed's latest research findings at the HEP-DART 2025 meeting underscores the significance of its work in liver disease treatment, further enhancing the company's competitive position in the market.

Galimedix Reports Excellent Phase 1 Results for GAL-101 with No Adverse Events
- Clinical Trial Success: Galimedix presented Phase 1 study results for GAL-101 at CTAD 2025, involving approximately 100 healthy volunteers, demonstrating excellent safety and tolerability with no dose-limiting adverse events, indicating the drug's potential in Alzheimer's treatment.
- Drug Penetration Capability: GAL-101 confirmed effective blood-brain barrier penetration with lumbar CSF concentrations after multiple doses, supporting a once-daily dosing regimen for future trials, which may enhance patient adherence to treatment.
- Future Research Planning: Following positive Phase 1 results, Galimedix is planning a Phase 2 proof-of-concept study in Alzheimer's disease, expected to include cognitive functional endpoints and biomarkers to capture early signs of cognitive improvement.
- Technological Innovation: As a small molecule targeting misfolded amyloid beta monomers to prevent toxic aggregate formation, GAL-101 shows broad application prospects in treating Alzheimer's disease, dry age-related macular degeneration, and glaucoma.








