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Completed

NCT Number: NCT05795517

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

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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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Beijing Tsinghua Changgung Hospital, Tsinghua University

Beijing, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must be willing to participate in the study and provide written informed consent.
  • Male or female aged 18 ≤ age < 65 at the time of signing the informed consent.
  • At the time of screening, patients who had not received lipid-regulation therapy within 6 weeks had fasting LDL-C≥3.34mmol/L(130mg/dL).
  • (BMI) ≥18kg/m2 and female subjects ≥45.0 kg and male subjects ≥50.0 kg.
  • During screening, fasting triglyceride (TG) <5.65 mmol/L.
  • During screening,MRI-PDFF≥8%.
  • Weight changes≤5% in the 4 weeks prior to screening.

Exclusion criteria

  • Did not discontinue any lipid-regulating therapy or any drug or supplement that may affect lipid levels 6 weeks before randomization or is expected to do so during the study period.
  • Homozygous familial hypercholesterolemia (HoFH) was diagnosed by genetic or clinical criteria.
  • Dyslipidemia caused by other diseases or drugs, such as rheumatoid arthritis, nephrotic syndrome, Cushing's syndrome, hypothyroidism, renal failure, systemic lupus erythematosus, glycogen accumulation, myeloma, lipodystrophy, acute porphyria, polycystic ovarian syndrome, etc
  • Before screening, LDL-C plasma exchange was performed within 12 months.
  • In the past, PCSK9 inhibitors, Lomitapide and Mipomersen were used for treatment.
  • uncontrolled hypertension had systolic blood pressure ≥160mmHg and/or diastolic blood pressure ≥100mmHg at screening/baseline.
  • type 1 diabetes, or newly diagnosed type 2 diabetes within 1 month, or poorly controlled type 2 diabetes, or who could not maintain the same hypoglycemic regimen during the study.
  • Stroke or transient ischemic attack (TIA), acute coronary syndrome, stable angina attack, severe deep vein thrombosis, or pulmonary embolism occurred in the 12 months prior to screening.
  • Major surgery (including but not limited to: coronary or other revascularization, coronary artery bypass surgery, and transplantation) within 12 months prior to screening or planned during the study period.
  • Chronic systemic disease or history, including but not limited to
  • Have a serious cardiopulmonary disease or history,Neurological disease or history,Autoimmune disease,Chronic digestive disease or history
  • Have thyroid disease or symptomatic abnormalities in thyroid function tests (e.g., thyroid stimulating hormone (TSH) < 1.0 x lower limit of normal (LLN) or > 1.5 x upper limit of normal (ULN))
  • History of malignancy (excluding cured basal cell carcinoma of the skin, carcinoma in situ, and papillary thyroid carcinoma) or history of antitumor therapy within 5 years prior to screening
  • Disease or medical history assessed by the investigator as likely to affect the study
  • Bariatric surgery within 12 months at the time of screening

Treatment and study plan

HSK31679 low dose

Drug

HSK31679 low dose and placebo of HSK31679 ,QD,oral,Day1 to week 12

HSK31679 medium dose

Drug

HSK31679 medium dose and placebo of HSK31679 ,QD,oral,Day1 to week 12

HSK31679 high dose

Drug

HSK31679 high dose and placebo of HSK31679 ,QD,oral,Day1 to week 12

Placebo

Drug

placebo ,QD,oral,Day1 to week 12

Ezetimibe 10mg

Drug

Ezetimibe 10mg+placebo of HSK31679 ,QD,oral,Day1 to week 12

Primary outcomes

  1. Percentage change in LDL-C from baseline at 12 week;

    Time frame: Baseline and Week 12

    Percentage change in fasting low-density lipoprotein cholesterol (LDL-C) from baseline after 12 weeks of treatment;

  2. Percentage change in MRI-PDFF from baseline at 12 week;

    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;

Secondary outcomes

  1. Percentage change in fasting LDL-C from baseline;

    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;

  2. 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 MRI-PDFF decreased by > 30%;

  3. Proportion of patients with LDL-C<3.34mmol/L(<130mg/dL)

    Time frame: Baseline and Week 12

    After 12 weeks of treatment, the proportion of patients with LDL-C<3.34mmol/L(<130mg/dL)

  4. Percentage change of fasting TG from baseline;

    Time frame: Week2,4,8,12

    After 2, 4, 8, 12 weeks of treatment, Percentage change of fasting triglycerides (TG), from baseline;

  5. Percentage change of fasting TC 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;

  6. Percentage change of fasting HDL-C 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;

  7. Percentage change in body weight from baseline

    Time frame: Baseline and Week 12

    Percentage change in body weight from baseline after 12 weeks of treatment.

  8. AUC0-τ of HSK31679 (All subjects)

    Time frame: up to 2,4,7 weeks

  9. Cmax of HSK31679 (All subjects)

    Time frame: up to 2,4,7 weeks

Sponsors and collaborators

Lead sponsor

Haisco Pharmaceutical Group Co., Ltd.

Industry

Registry information

Official study title

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

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Apr 3, 2023
Registry last updated
Apr 9, 2024

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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