drugset / Trial / NCT03413462

Efficacy and Safety Study of HS-25 in Chinese Adults With Primary Hypercholesterolemia

NCT03413462

Phase 3 Completed 374 enrolled Zhejiang Hisun Pharmaceutical Co. Ltd.
RandomizedParallel-groupTriple-blindTreatment

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 adults with primary hypercholesterolemia; To determine the safety of HS-25 (20mg) in subjects with LDL-C

Timeline

Start
2016-04-12
Primary completion
2018-04-20
Completion
2018-09-20

Drugs

EvaluationDrugModalityDoseRoute
Comparator HYZETIMIBE Small molecule 20 mg

Indications