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Clinical Trial Summary

To determine the efficacy of HS-25 (20mg) in reducing low density lipoprotein-cholesterol (LDL-C) levels after a 12-week period of treatment in combination with Atorvastatin in subjects with hypercholesterolemia and coronary heart diseases; To determine the safety of HS-25 (20mg) combination with Atorvastatin in subjects with hypercholesterolemia and coronary heart diseases


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03433196
Study type Interventional
Source Zhejiang Hisun Pharmaceutical Co. Ltd.
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Status Completed
Phase Phase 3
Start date June 7, 2016
Completion date October 10, 2018