Friday, June 10, 2022 3:27:42 PM
"Conclusions: The primary endpoint (PDFF) and secondary endpoints (cT1) were met for the 350 mg group and moderate to severe fibro-inflammation by cT1 350 mg subgroup at baseline. The pooled 350 + 700 mg group also had significant reductions in PDFF, cT1 vs placebo. Treatment with leronlimab was well tolerated. These results are supportive of further trials with leronlimab for NASH."
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My comments are just my opinions and should NOT be taken as investment advice.
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