drugset / Trial / NCT05260411

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

NCT05260411

Phase 3 Completed 246 enrolled Akeso
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2022-01-26
Primary completion
2022-12-19
Completion
2022-12-19

Drugs

EvaluationDrugModalityDoseRoute
Subject AK102 Monoclonal antibody 450 mg Subcutaneous
Subject AK102 Monoclonal antibody 600 mg Subcutaneous

Indications