Boehringer Ingelheim said on Monday that its “double G” metabolic dysfunction-associated steatohepatitis (MASH) drug delivered positive topline results in a Phase II trial.
The company said that 83% of participants in the survodutide arm passed the study’s biopsy-driven primary endpoint, compared with 18.2% with placebo (p<0.0001) at 48 weeks. Survodutide, which Boehringer “co-invented” with Zealand Pharma, is a glucagon/GLP-1 receptor dual agonist administered once weekly via a subcutaneous injection.
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