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  • 24 Jun 2025

MTVA: DA-1241 in Combination with Efruxifermin Shows Additive Hepatoprotective Effects in Mouse MASH Model


MetaVia Inc. (MTVA:NAS) | 0 0 0.0%


  • Zacks Small Cap Research
    • David Bautz

    • 6 pages


 

On June 21, 2025, MetaVia Inc. (MTVA) announced the presentation of preclinical data for DA-1241, the company's novel GPR119 agonist, that showed hepatoprotective effects when administered in combination with Efruxifermin, a fibroblast growth factor 21 (FGF21) analogue, in a mouse model of metabolic dysfunction-associated steatohepatitis (MASH). The results were presented in a poster session at the American Diabetes Association 85th Scientific Sessions. The data showed that 94% of mice receiving the combination therapy achieved a =2-point improvement in the non-alcoholic fatty liver disease (NAFLD) activity score and immunohistochemistry revealed significantly reduced inflammatory and fibrotic gene expression in the liver. These results further support utilizing DA-1241 as part of a combination MASH therapy with an agent that has a complementary mechanism of action.

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MTVA: DA-1241 in Combination with Efruxifermin Shows Additive Hepatoprotective Effects in Mouse MASH Model


MetaVia Inc. (MTVA:NAS) | 0 0 0.0%


  • Published: 24 Jun 2025
  • Author: David Bautz
  • Pages: 6
  • Zacks Small Cap Research


On June 21, 2025, MetaVia Inc. (MTVA) announced the presentation of preclinical data for DA-1241, the company's novel GPR119 agonist, that showed hepatoprotective effects when administered in combination with Efruxifermin, a fibroblast growth factor 21 (FGF21) analogue, in a mouse model of metabolic dysfunction-associated steatohepatitis (MASH). The results were presented in a poster session at the American Diabetes Association 85th Scientific Sessions. The data showed that 94% of mice receiving the combination therapy achieved a =2-point improvement in the non-alcoholic fatty liver disease (NAFLD) activity score and immunohistochemistry revealed significantly reduced inflammatory and fibrotic gene expression in the liver. These results further support utilizing DA-1241 as part of a combination MASH therapy with an agent that has a complementary mechanism of action.

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