drugset / Trial / NCT05795517

Study of HSK31679 in Subjects With Hypercholesterolemia With Nonalcoholic Fatty Liver Disease(NAFLD)

NCT05795517

Phase 2 Completed 210 enrolled Haisco Pharmaceutical Group Co., Ltd.
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

EvaluationDrugModalityDoseRoute
Comparator Ezetimibe Unknown 10 mg Oral
Subject HSK31679 Unknown 40 mg Oral
Subject HSK31679 Unknown 80 mg Oral
Subject HSK31679 Unknown 160 mg Oral

Indications