drugset / Trial / NCT01763827

Monoclonal Antibody Against PCSK9 to Reduce Elevated LDL-C in Subjects Currently Not Receiving Drug Therapy for Easing Lipid Levels-2

NCT01763827 ↗

Phase 3 Completed 615 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective was to evaluate the effect of 12 weeks of evolocumab subcutaneous (SC) monotherapy every 2 weeks (Q2W) and monthly (QM), compared with placebo and ezetimibe, on percent change from baseline in low-density lipoprotein cholesterol (LDL-C) in adults with a 10-year Framingham risk score of 10% or less.

Timeline

Start
2013-01-21
Primary completion
2013-10-10
Completion
2013-10-29

Outcome

Met primary endpoint

registry Placebo Q2W vs Evolocumab Q2W; p <0.001; LS Mean Treatment Difference -57.14 (95% CI -61.14 to -53.14) NCT01763827 ↗

registry Placebo Q2W vs Evolocumab Q2W; p <0.001; LS Mean Treatment Difference -56.50 (95% CI -59.95 to -53.04) NCT01763827 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Evolocumab Monoclonal antibody 140 mg Subcutaneous
Subject Evolocumab Monoclonal antibody 420 mg Subcutaneous
Comparator Ezetimibe Unknown 10 mg Oral

Indications