Clinical Trial

A Study to Evaluate the Safety, Efficacy of SYH2053 in Chinese Participants With Non-familial Hypercholesterolemia and Mixed Hyperlipidemia

Completed Phase 2
View on ClinicalTrials.gov →
Summary
The purpose of this study is to compare the effectiveness, safety of SYH2053 in Participants with primary hypercholesterolemia or mixed dyslipidemia. A total of 156 Participants were actually enrolled
Trial Details
NCT Number NCT07421232
Lead Sponsor CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.
Conditions Hypercholesterolemia and Mixed Hyperlipidemia
Enrollment 156 participants
Start Date 2024-12-03
Primary Completion 2025-08-30 (estimated)
Study Completion 2026-02-12 (estimated)
Updated on ClinicalTrials.gov 2026-02-19