Overview

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.