drugset / Trial / NCT05795517
Study of HSK31679 in Subjects With Hypercholesterolemia With Nonalcoholic Fatty Liver Disease(NAFLD)
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this study is to assess the efficacy and safety of HSK31679 tablets compared with placebo in reducing low-density lipoprotein cholesterol (LDL-C) and MRI-PDFF after 12 weeks of treatment in patients with hypercholesterolemia and non-alcoholic fatty liver disease (NAFLD).
Timeline
- Start
- 2023-04-26
- Primary completion
- 2024-02-20
- Completion
- 2024-03-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Ezetimibe | Unknown | 10 mg | Oral |
| Subject | HSK31679 | Unknown | 40 mg | Oral |
| Subject | HSK31679 | Unknown | 80 mg | Oral |
| Subject | HSK31679 | Unknown | 160 mg | Oral |