drugset / Trial / NCT01763918

Reduction of LDL-C With PCSK9 Inhibition in Heterozygous Familial Hypercholesterolemia Disorder Study-2

NCT01763918

Phase 3 Completed 331 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective was to evaluate the effect of 12 weeks of evolocumab subcutaneously once every 2 weeks (Q2W) and once monthly (QM), compared with placebo, on percent change from baseline in low-density lipoprotein cholesterol (LDL-C) in adults with heterozygous familial hypercholesterolemia (HeFH).

Timeline

Start
2013-02-07
Primary completion
2013-11-27
Completion
2013-12-19

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Evolocumab Monoclonal antibody 140 mg Subcutaneous
Subject Evolocumab Monoclonal antibody 420 mg Subcutaneous

Indications