Novo Nordisk semaglutide phase 3 trial for MASH meets primary endpoints

seekingalpha
2024-11-20

Mohammed Haneefa Nizamudeen

  • A phase 3 trial examining Novo Nordisk's (NVO) GLP-1 medicine semaglutide as a treatment for metabolic dysfunction-associated steatohepatitis (MASH) met its primary endpoints.
  • Those endpoints were significant improvement in liver fibrosis with no worsening of steatohepatitis, and no worsening of liver fibrosis in those with MASH compared to placebo.
  • In the study, 2.4 mg semaglutide was given subcutaneously once a week.
  • Results from part 1 of the ESSENCE trial showed that at week 72, 62.9% of people treated with semaglutide achieved resolution of steatohepatitis with no worsening of liver fibrosis compared to 34.1% on placebo. Also, 37% of people treated with semaglutide 2.4 mg achieved improvements in liver fibrosis with no worsening of steatohepatitis compared to 22.5% on placebo.
  • A secondary endpoint found 32.8% of those on semaglutide 2.4 mg achieved both resolution of steatohepatitis with improvements in liver fibrosis vs. 16.2% of placebo patients.
  • Semaglutide is also sold by Novo as a type 2 diabetes medicine under the name Ozempic and as a weight loss treatment called Wegovy.

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