A Randomized, Double-blind, Placebo-controlled Study of ZSP1601 in Adult Subjects With Nonalcoholic Steatohepatitis (NASH)

Inclusion Criteria:

1. NASH histological diagnosis on a liver biopsy performed ≤ 24 weeks beforerandomization, and NAS≥4 (at least 1 point each in inflammation and ballooning), andfibrosis score F2 or F3, and no other chronic liver disease

2. Subjects having given her/his written informed consent

3. Good compliance with the protocol and agree to have liver biopsy performed

4. Subjects (including their partners) agreed to use effective contraception throughoutthe study period and up to 24 weeks after discontinuation

Exclusion Criteria:

1. History of cirrhosis or liver biopsy suggestive of cirrhosis

2. Metabolic surgery or new technology treatment for weight loss within 5 years priorto randomization or planned during the study period

3. Type 1 diabetes

4. HIV infection

5. Patients with severe or uncontrollable underlying diseases, unsuitable for treatmentwith ZSP1601, unable to complete study follow-up, or likely to affect the evaluationof trial results judged by investigator

6. Previous malignancy within 5 years

7. Treatment with hepatoprotective drugs

8. Excessive alcohol consumption for 12 or more consecutive weeks within 1 year priorto screening

9. Pregnant and lactating women or those with a positive serum pregnancy test.