Biopharma Transcript

MetaVia Inc. MTVA

Nasdaq · Phase 2 · cardio-renal-metabolic · small molecule · EDGAR · Updated Oct 24, 2026

MetaVia Inc. (Nasdaq: MTVA) is a cardio-renal-metabolic drug developer. Its lead program, vanoglipel (DA-1241), is in Phase 2 for MASH / metabolic disease. Its next catalyst on record is vanoglipel: finalize Phase 2a Clinical Study Report (Q4 2026).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: vanoglipel — finalize Phase 2a Clinical Study Report (Q4 2026). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
vanoglipel (DA-1241)MASH (Phase 2a completed; end-of-Phase 2 meeting being scheduled)small moleculePhase 2
DA-1726obesity (GLP-1/glucagon dual agonist), Phase 1 Part 3a/3bprotein/peptidePhase 1

Recent results and decisions

  1. Jan 5, 2026
    positive Non-titrated 48 mg cohort showed 9.1% mean weight loss at day 54, 9.8 cm waist reduction (p=0.022), and 23.7% liver stiffness reduction; no treatment-related discontinuations.By Day 26, patients receiving DA-1726 achieved a statistically significant average weight reduction of 6.1% (14.6 lbs.) (p=0.003) Filing
  2. Nov 6, 2025
    positive DA-1726 32 mg cohort in Phase 1 MAD showed mean weight loss of 4.3% (max 6.3%) at day 26 with no treatment-related discontinuations (re-presented in investor deck).Day 26 shown dose dependent and compelling BWL shown in 8 mg, 16 mg and 32 mg Filing
  3. Nov 6, 2025
    met Vanoglipel Phase 2a primary endpoint met with direct hepatic effects and significant HbA1c reductions vs placebo (re-presented in investor deck).Phase 2a Primary End Point Met and showed direct hepatic effects Filing

For subscribers

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