Beijing Tsinghua Changgung Hospital, Tsinghua University
Beijing, China
NCT Number: NCT05795517
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).
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Notify Me18 year–65 year
All sexes
Interventional
Phase 2
Beijing, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
HSK31679 low dose and placebo of HSK31679 ,QD,oral,Day1 to week 12
HSK31679 medium dose and placebo of HSK31679 ,QD,oral,Day1 to week 12
HSK31679 high dose and placebo of HSK31679 ,QD,oral,Day1 to week 12
placebo ,QD,oral,Day1 to week 12
Ezetimibe 10mg+placebo of HSK31679 ,QD,oral,Day1 to week 12
Time frame: Baseline and Week 12
Percentage change in fasting low-density lipoprotein cholesterol (LDL-C) from baseline after 12 weeks of treatment;
Time frame: Baseline and Week 12
Percentage change of MRI-PDFF(change in liver fat content by nuclear magnetic resonance - Proton Density Fat Fraction) from baseline after 12 weeks of treatment;
Time frame: Week2,4,8
Percentage change in fasting low-density lipoprotein cholesterol (LDL-C) from baseline after 2, 4, and 8 weeks of treatment;
Time frame: Baseline and Week 12
After 12 weeks of treatment, the proportion of patients with MRI-PDFF decreased by > 30%;
Time frame: Baseline and Week 12
After 12 weeks of treatment, the proportion of patients with LDL-C<3.34mmol/L(<130mg/dL)
Time frame: Week2,4,8,12
After 2, 4, 8, 12 weeks of treatment, Percentage change of fasting triglycerides (TG), from baseline;
Time frame: Week2,4,8,12
After 2, 4, 8, 12 weeks of treatment, Percentage change of fasting total cholesterol (TC) from baseline;
Time frame: Week2,4,8,12
After 2, 4, 8, 12 weeks of treatment, Percentage change of fasting high-density lipoprotein cholesterol (HDL-C) from baseline;
Time frame: Baseline and Week 12
Percentage change in body weight from baseline after 12 weeks of treatment.
Time frame: up to 2,4,7 weeks
Time frame: up to 2,4,7 weeks
Haisco Pharmaceutical Group Co., Ltd.
Industry
A Phase 2 ,Multicentre, Randomised, Double Blind Double Simulation, Placebo and Positive Controlled Study to Evaluate the Efficacy and Safety of HSK31679 in Patients With Hypercholesterolemia With Non-alcoholic Fatty Liver Disease
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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