drugset / Trial / NCT03399370

Inclisiran for Participants With Atherosclerotic Cardiovascular Disease and Elevated Low-density Lipoprotein Cholesterol

NCT03399370 ↗

Phase 3 Completed 1561 enrolled The Medicines Company
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a Phase III, placebo-controlled, double-blind, randomized study in participants with ASCVD and elevated LDL-C despite maximum tolerated dose of LDL-C lowering therapies to evaluate the efficacy, safety, and tolerability of subcutaneous (SC) inclisiran injection(s). The study will be a multicenter study in the United States.

Timeline

Start
2017-12-21
Primary completion
2019-09-10
Completion
2019-09-17

Outcome

Met primary endpoint

registry analysis (superiority test); Inclisiran vs Placebo; p <.0001; Mean Difference (Final Values) -57.64 (95% CI -60.86 to -54.43) NCT03399370 ↗

registry analysis (superiority test); Inclisiran vs Placebo; p <0.0001; Mean Difference (Final Values) -53.78 (95% CI -56.23 to -51.33) NCT03399370 ↗

release “For the primary endpoints of ORION-10, inclisiran delivered mean placebo-adjusted percentage change in LDL-C reductions of 52% ( P <.0001) at 17 months” novartis.com ↗

release “For the primary endpoints of ORION-10, Leqvio delivered mean placebo-adjusted percentage change in LDL-C reductions of 52% ( P <.0001) at 510 days” novartis.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Inclisiran Small interfering RNA (siRNA) 300 mg Subcutaneous