A Study to Evaluate the Efficacy and Safety of AK102 Q6W in Patients With Hyperlipidemia

• Status: Recruiting
• Trial end date: 2022-12-31
• Target enrollment: 0
• Participant gender: All

Summary

This is a randomized, double-blind, placebo-controlled phase # clinical study evaluating the efficacy and safety of AK102 Q6W in patients with primary hypercholesterolemia and mixed hyperlipidemia.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Akeso

Criteria

Inclusion Criteria:

1. Subject understand and voluntarily sign the written Inform Consent Form (ICF).

2. Male or female ≥ 18 to ≤ 80 years of age.

3. The fasting serum LDL-C level of subjects did not meet the treatment goal after at least 4 weeks of stable lipid-lowering background treatment.

4. TG ≤ 4.5 mmol/L (400 mg/dl)

Exclusion Criteria:

1. Known homozygous familial hypercholesterolemia.

2. Received PCSK9 inhibitors within 6 months before randomization.

3. Known sensitivity to PCSK9 inhibitors and any substances to be administered.

4. Severe renal dysfunction.

5. Previously received organ transplantation.

6. Uncontrolled hypothyroidism or hyperthyroidism.

7. Uncontrolled hypertension.

8. Known hyperlipidemia secondary to comorbidity, including nephrotic syndrome, cholestatic liver failure, etc.

9. History of malignancy of any organ system within the past 5 years.