drugset / Trial / NCT06109831

Evaluate the Efficacy and Safety of SHR-1918 in Patients With Hyperlipidemic

NCT06109831 ↗

Phase 2 Completed 335 enrolled Beijing Suncadia Pharmaceuticals Co., Ltd
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Multicenter, Randomized, Double-Blind, Placebo-Parallel-Controlled, Phase II Clinical Stud to assess the reduction of low-density lipoprotein cholesterol (LDL-C) by SHR-1918 in patients with Hyperlipidemic.

Timeline

Start
2023-11-24
Primary completion
2025-07-04
Completion
2025-07-04

Drugs

EvaluationDrugModalityDoseRoute
Subject SHR-1918 Monoclonal antibody 150 mg Subcutaneous
Subject SHR-1918 Monoclonal antibody 300 mg Subcutaneous
Subject SHR-1918 Monoclonal antibody 600 mg Subcutaneous

Indications