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A total of 95 NASH patients were screened, of which 37 patients were randomized, and 36 NAFLD patients were enrolled in three cohorts. Each cohort included 12 patients, 9 of whom received ZSP1601 50 mg QD, 50 mg BID, or 100 mg BID, and 3 of whom received matching placebos for 28 days. All the 36 patients completed the clinical trial and were scheduled to receive a 14-day treatment-free follow-up.

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