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The two primary endpoints of the trial at week 52 were defined as the resolution of NASH with non-worsening fibrosis, and an improvement (reduction) in at least one stage of fibrosis with non-worsening of the MASLD activity score
type:serum-ampoule
Size:40ml
A pivotal 2007 study published in the Journal of Physiology and Pharmacology examined rats with experimentally induced esophagitis and sphincter failure
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