Akero’s drug misses the mark in severe form of NASH
Akero Therapeutics, part of a cohort of biotechs attempting to mark a turnaround in NASH drug development, did not pass the bar in a Phase IIb test of patients with cirrhosis, the most severe form of the fatty liver disease that is also known as stage F4.
The South San Francisco biotech’s lead drug, dubbed efruxifermin, was not statistically significant in beating out placebo in improving liver scarring without worsening of NASH, Akero said before Tuesday’s opening bell. At a 36-week analysis, the p-values were 0.38 and 0.28 for the low and high doses, respectively, according to an investor presentation.
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