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NCT03008070 - NATIVE - Lanifibranor vs placebo & Non-alcoholic Steatohepatitis (NASH): The percentage of patients who had a decrease of at least 2 points in the SAF-A score without worsening of fibrosis was significantly higher with the 1200-mg dose of lanifibranor than with placebo. These findings support further assessment of lanifibranor in phase III trials
see also:
Peroxisome proliferator-activated receptor (PPAR) agonists & Non-alcoholic Steatohepatitis (NASH)
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