RecruitingPhase 3NCT07465263

A Study to Evaluate the SYH2053 Injection in Patients With Heterozygous Familial Hypercholesterolemia (HeFH)

A Study to Evaluate the SYH2053 Injection in Patients With Heterozygous Familial Hypercholesterolemia (HeFH): A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase Ⅲ Clinical Trial


Sponsor

CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.

Enrollment

135 participants

Start Date

Mar 31, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

Heterozygous Familial Hypercholesterolemia (HeFH) is an autosomal dominant disorder characterized by markedly elevated low-density lipoprotein cholesterol (LDL-C) and increased risk of atherosclerotic cardiovascular disease (ASCVD). This trial aims to evaluate the SYH2053 Injection in patients with HeFH.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Placebo Injection and a drug called SYH2053 Injection for people with heterozygous familial hypercholesterolemia (hefh). The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSYH2053 Injection

Administered by subcutaneous injection.

DRUGPlacebo Injection

Administered by subcutaneous injection. The placebo is identical to SYH2053 Injection in appearance.


Locations(1)

Peking University First Hospital

Beijing, Beijing Municipality, China

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NCT07465263


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