drugset / Trial / NCT01763866

LDL-C Assessment With PCSK9 Monoclonal Antibody Inhibition Combined With Statin Therapy-2

NCT01763866

Phase 3 Completed 2067 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective was to evaluate the effect of 12 weeks of evolocumab administered subcutaneously every 2 weeks (Q2W) and monthly (QM) when used in combination with a statin, compared with placebo, on percent change from baseline in low-density lipoprotein cholesterol (LDL-C) in patients with primary hypercholesterolemia and mixed dyslipidemia.

Timeline

Start
2013-01-15
Primary completion
2013-11-12
Completion
2013-12-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Evolocumab Monoclonal antibody 140 mg Subcutaneous
Subject Evolocumab Monoclonal antibody 420 mg Subcutaneous
Comparator Ezetimibe Unknown 10 mg Oral
Background Atorvastatin Small molecule 10 mg Oral
Background Atorvastatin Small molecule 80 mg Oral
Background Rosuvastatin Small molecule 5 mg Oral
Background Rosuvastatin Small molecule 40 mg Oral
Background Simvastatin Small molecule 10 mg Oral
Background Simvastatin Small molecule 20 mg Oral
Background Simvastatin Small molecule 40 mg Oral

Indications