MetaVia Reveals DA-1241 Outcomes on Liver Health and Diabetes
Exciting Developments in Liver Health Treatment
MetaVia Inc. (Nasdaq: MTVA), a pioneering biotechnology company, recently unveiled significant findings from its Phase 2a clinical trial concerning DA-1241, a G-Protein-Coupled Receptor 119 (GPR119) agonist. This compound aims to benefit patients struggling with metabolic dysfunction-associated steatohepatitis (MASH). The results suggest that DA-1241 not only protects the liver but also regulates glucose levels effectively, providing hope for patients facing these health challenges.
Key Findings on Liver Health Markers
One standout observation from the trial was that DA-1241 substantially decreased plasma alanine transaminase (ALT) levels. After 16 weeks of treatment, participants receiving DA-1241 100 mg experienced an impressive average reduction of 22.8 U/L in ALT. This decline indicates fewer markers of liver injury and could reflect the compound's protective effects against liver damage.
Moreover, the Controlled Attenuation Parameter (CAP) score, which assesses liver fat content, improved by 23.0 dB/m, demonstrating that DA-1241 effectively reduces liver fat. Improvements in systemic inflammatory and fibrosis biomarkers further reinforced the beneficial effects of DA-1241 on liver health.
Clinical Trial Overview
In this trial, 109 subjects were involved, each diagnosed with presumed MASH. They were randomly assigned to receive DA-1241 in various dosages or a placebo for 16 weeks. The primary goal was to measure ALT changes from the baseline level. The results confirmed the efficacy of DA-1241 as a promising treatment for MASH, highlighting its dual capability in promoting liver health while controlling glucose levels.
Hyung Heon Kim, MetaVia’s President and CEO, expressed enthusiasm about the study's outcome, emphasizing that DA-1241 is the first oral GPR119 agonist showcasing these dual effects. The data indicated that patients not only benefitted from reduced liver injury and inflammation but also enjoyed improved glycemic control.
Dramatic Improvements in Glycemic Control
Patients receiving DA-1241 displayed substantial improvements in hemoglobin A1c (HbA1c) levels—decreasing by 0.37%, 0.41%, and 0.54% at weeks 4, 8, and 16, respectively. For those with existing type 2 diabetes, the HbA1c reduction averaged an even more striking 1.08%p. Such outcomes highlight the medication's effectiveness in managing glucose levels, especially given that nearly half of the trial participants were non-diabetic.
The trial proved DA-1241's excellent tolerability, with no serious adverse events leading to treatment discontinuation observed. This aspect presents DA-1241 not only as an effective agent in treating metabolic concerns but also as a safe option for patients.
Highlighted Presentation at EASL Congress 2025
The findings from this groundbreaking study were presented as a late-breaking poster during the European Association for the Study of the Liver (EASL) Congress 2025. Insights from this congress are vital as they underscore emerging treatment modalities in the ever-evolving landscape of liver diseases.
Future Directions and Expanded Research Potential
Looking ahead, MetaVia is committed to further exploring the therapeutic potential of DA-1241, considering both monotherapy and combination options for managing MASH and type 2 diabetes. The company is actively pursuing additional studies to broaden DA-1241's applicability and effectiveness for patients across various stages of metabolic disease.
Frequently Asked Questions
What is DA-1241 and its primary use?
DA-1241 is a GPR119 agonist developed to treat metabolic dysfunction-associated steatohepatitis (MASH) and offers both liver protection and glucose regulation.
How does DA-1241 affect liver health?
DA-1241 significantly reduces plasma ALT levels and liver fat content, as indicated by improvements in CAP scores and inflammatory biomarkers.
What was the outcome of the Phase 2a clinical trial?
The trial demonstrated that DA-1241 effectively improves liver health and glucose control in patients with presumed MASH, showcasing promising efficacy and safety.
Why is MetaVia's research on DA-1241 important?
This research highlights a novel approach to tackling liver health issues while managing glucose levels, potentially addressing key concerns in metabolic diseases.
Will DA-1241 be further developed?
Yes, MetaVia plans to advance DA-1241's development, exploring the possibility of using it as a standalone or combination therapy for MASH and related conditions.
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