drugset / Trial / NCT01763905

Goal Achievement After Utilizing an Anti-PCSK9 Antibody in Statin Intolerant Subjects -2

NCT01763905 ↗

Phase 3 Completed 307 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective was to evaluate the effect of 12 weeks of subcutaneous (SC) evolocumab every 2 weeks (Q2W) and monthly (QM), compared with ezetimibe, on percent change from baseline in low-density lipoprotein cholesterol (LDL-C) in hypercholesterolemic adults unable to tolerate an effective dose of a statin (HMG-CoA (5-hydroxy-3-methylglutaryl-coenzyme A) reductase inhibitors).

Timeline

Start
2013-01-24
Primary completion
2013-11-19
Completion
2013-11-19

Outcome

Met primary endpoint

registry analysis (unspecified test); Ezetimibe (Q2W) vs Evolocumab Q2W; p <0.001; LS Mean Treatment Difference -38.06 (95% CI -43.73 to -32.99) NCT01763905 ↗

registry analysis (unspecified test); Ezetimibe (QM) vs Evolocumab QM; p <0.001; LS Mean Treatment Difference -37.55 (95% CI -42.16 to -32.94) NCT01763905 ↗

registry analysis (unspecified test); Ezetimibe (Q2W) vs Evolocumab Q2W; p <0.001; LS Mean Treatment Difference -36.90 (95% CI -42.26 to -31.55) NCT01763905 ↗

registry analysis (unspecified test); Ezetimibe (QM) vs Evolocumab QM; p <0.001; LS Mean Treatment Difference -38.69 (95% CI -43.06 to -34.22) NCT01763905 ↗

Publications

Drugs

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

Indications