A Dose-exploration Study of EDP167 in HoFH

Exclusion Criteria19

• Allergic to the drug in this study, its components or similar drugs.
• Used any antisense oligonucleotide (ASO) or small interfering nucleic acid (siRNA) drugs within 12 months prior to randomization.
• Received treatment targeting ANGPTL3 or Apolipoprotein C3 (ApoC3), or have participated in other clinical trials within 6 months or 5 half-life (whichever longer) prior to screening.
• Received health supplements or other medications that have been used for lipid-lowering purposes within 4 weeks prior to screening.
• Received Lipoprotein apheresis within 8 weeks prior to screening.
• A weight change of \>10% within 4 weeks prior to randomization, or planning to undergo weight-loss surgery or weight intervention treatment during the study period.
• Starting a new diet plan or having significant differences from the previous diet within 4 weeks prior to randomization.
• Presence of diseases that would affect lipid or lipoprotein levels, such as nephrotic syndrome, severe liver diseases, Cushing's syndrome, hypothyroidism or hyperthyroidism, etc., which are poorly controlled, and in the opinion of the Investigator will interfere with the accurate assessment of the study results.
• Had New York Heart Association (NYHA) grade III-IV heart failure within 12 months prior to randomization, or acute coronary syndrome or stroke within 6 months prior to randomization.
• Performed coronary intervention within 6 months prior to randomization, or plan to perform coronary intervention during the study.
• Have a history of major surgery within 3 months prior to screening, or plan to undergo major surgery during the study.
• With a history of malignancy, unless it is believed to have been cured by adequate treatment and there is no evidence of recurrence for at least 3 years.
• Clinical evidence of active infections or other major or poorly controlled serious diseases, any other conditions that in the opinion of the Investigator may interfere with the study results or put the subjects at excessive risk.
• Have a history of current existence of alcohol or drug abuse per evaluation of the investigator.
• Uncontrolled hypertension at screening (blood pressure \>160/100 mmHg).
• Subjects with any of the following laboratory abnormalities at screening: a) fasting serum TG≥5.6 mmol/L; b) Glycosylated hemoglobin A1C (HbA1c)\>8.5%; c) alanine aminotransferase (ALT) or aspartate aminotransferase (AST) or gamma-glutamyl transpeptidase (GGT)\>1.5×ULN (Upper Limit Of Normal), total bilirubin (TBIL)\>2×ULN; d) prothrombin time (PT) or activated partial thromboplastin time (APTT) or International Normalized Ratio (INR) clinically significant abnormal; e) Hepatitis B surface antigen (HBsAg) or antibody to hepatitis C virus (HCVAb) or human immunodeficiency virus (HIV) positive; f) estimated glomerular filtration rate (eGFR)\<30 mL/min/1.73m2.
• Donated or lost blood ≥400 mL within 3 months prior to screening.
• Women who are pregnant, breastfeeding or planning for pregnancy.
• Other conditions that the Investigator would consider the subject is not suitable to participate in this study.