drugset / Trial / NCT02597127

Trial to Evaluate the Effect of ALN-PCSSC Treatment on Low Density Lipoprotein Cholesterol (LDL-C)

NCT02597127 ↗

Phase 2 Completed 501 enrolled The Medicines Company
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is a Phase II, placebo-controlled, double-blind, randomized trial in 480 participants with atherosclerotic cardiovascular disease (ASCVD) or ASCVD-risk equivalents (for example, diabetes and familial hypercholesterolemia) and elevated LDL-C despite maximum tolerated dose of LDL-C lowering therapies to evaluate the efficacy, safety, and tolerability of ALN-PCSSC injection(s).

Timeline

Start
2016-01
Primary completion
2017-06-07
Completion
2017-06-07

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo (Single Dose) vs 200 mg (Single Dose); p <0.0001 NCT02597127 ↗

release “For all dose groups, at all time points, differences in the primary (LDL-C) and secondary (PCSK9) endpoints between inclisiran and placebo were statistically significant (p < 0.0001).” alnylam.com ↗

Publications

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
Subject Inclisiran Small interfering RNA (siRNA) 500 mg Subcutaneous