drugset / Trial / NCT04666298
Study of Efficacy and Safety of Inclisiran in Japanese Participants With High Cardiovascular Risk and Elevated LDL-C
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This was a placebo-controlled, double-blind, randomized trial in Japanese participants with history of coronary artery disease (CAD) or participants categorized in 'high risk' by JAS 2017 guideline, or Japanese participants with heterozygous familial hypercholesterolemia (HeFH) and elevated Low-density lipoprotein cholesterol (LDL-C) despite maximum tolerated dose of statin(s) to evaluate the efficacy, safety, tolerability, and PK of subcutaneous inclisiran injection(s).
Timeline
- Start
- 2021-01-29
- Primary completion
- 2022-04-18
- Completion
- 2022-10-19
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Inclisiran | Small interfering RNA (siRNA) | 100 mg | Subcutaneous |
| Subject | Inclisiran | Small interfering RNA (siRNA) | 200 mg | Subcutaneous |
| Subject | Inclisiran | Small interfering RNA (siRNA) | 300 mg | Subcutaneous |