A Study to Assess the Safety, Tolerability, Pharmacokinetics and Efficacy of CS0159 in Subjects With NASH

This will be a multicenter, double-blind, randomized, placebo-controlled, dose-ranging study to evaluate the safety, tolerability, PKs, and efficacy of CS0159 in the treatment of patients with NASH over 12 weeks.

Inclusion criteria

• Patients who meet the diagnosis of NASH.
• Evidence of metabolic syndrome, except for those patients with biopsy-proven NASH.
• Body mass index (BMI) >25 kg/m2, NOTE: for Asian-Americans BMI >23 kg/m2.
• Stable use of other antidiabetic, weight loss, or lipid-modifying medications for at least 12 weeks prior to randomization.

Exclusion criteria

• Use of other investigational drugs within 5 half-lives of enrollment, or within 30 days, whichever is longer.
• Previous exposure to farnesoid X receptor (FXR) agonists 3 months prior to the first dosing.
• Current or within 6 months of screening use of drugs associated with steatosis, including but not limited to eg, methotrexate, amiodarone, high-dose estrogen, tamoxifen, long term systemic steroids, anabolic steroids, valproic acid.
• Prothrombin time international normalized ratio >1.3, unless due to therapeutic anticoagulation.
• Total bilirubin >upper limit of normal (ULN; except for patients with Gilbert's syndrome with a normal direct bilirubin value and normal reticulocyte count).

Platelet count <140 000/mm³, absolute neutrophil count <1500 cells/mm3, or total

• white blood cells <3000 cells/mm3.
• Alanine aminotransferase and aspartate aminotransferase (AST) >5 × ULN, or alkaline phosphatase (ALP) >1.5 × ULN.
• Weight changes >10% in 6 months prior to screening, or weight changes >5% from the screening MRI-PDFF to randomization or from the time of the diagnostic liver biopsy to randomization, whichever is longer.
• Poorly controlled hypertension (systolic >160 mm Hg, or diastolic blood pressure >100 mm Hg - mean of 3 measurements).
• Uncontrolled diabetes mellitus (hemoglobin A1c >10.0% during screening).