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A phase 2, adaptive randomized, double-blind, placebo-controlled, multicenter, 52-week study of HM15211 in patients with biopsy-confirmed non-alcoholic steatohepatitis - Study design and rationale of HM-TRIA-201 study

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Blood was drawn before (0 min) and after the intraperitoneal administration of glucose (2.0 g/kg body weight) at intervals of 2, 6, 10, 30, 60, and 120 min ( n = 34 per time point)

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