drugset / Trial / NCT04666298

Study of Efficacy and Safety of Inclisiran in Japanese Participants With High Cardiovascular Risk and Elevated LDL-C

NCT04666298

Phase 2 Completed 312 enrolled Novartis Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
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