drugset / Trial / NCT03413462
Efficacy and Safety Study of HS-25 in Chinese Adults With Primary Hypercholesterolemia
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | HYZETIMIBE | Small molecule | 20 mg | — |