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A Study to Determine the Safety, Tolerability, and Efficacy of SHR-1209 in Patients With Familial Hypercholesterolemia

Familial Hypercholesterolemia Clinical Trial

Official title:
Open-label, Single-arm, Multicentre Study to Evaluate Efficacy and Safety of SHR-1209 in Subjects With Homozygous Familial Hypercholesterolemia

Clinical Trial Summary

The study is being conducted to evaluate the efficacy, safety and tolerability of SHR-1209 in subjects with familial hypercholesterolemia. 8 eligible patients (aged ≥18 years) with familial hypercholesterolemia, on stable maximum tolerable dose lipid-regulating therapy for at least 28 days, to receive subcutaneous SHR-1209, follow up 8 weeks. The primary endpoint was percentage change in LDL cholesterol from baseline at week 12 .

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04455581
Study type Interventional
Source Jiangsu HengRui Medicine Co., Ltd.
Contact Bin Zhang, Medial Manager
Phone +86 13671548369
Email zhangbin@hrglobe.cn
Status Not yet recruiting
Phase Phase 2
Start date September 1, 2020
Completion date August 31, 2021
View Details
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