drugset / Trial / NCT01375751

Reduction of Low-Density Lipoprotein Cholesterol (LDL-C) With PCSK9 Inhibition in Heterozygous Familial Hypercholesterolemia Disorder Study

NCT01375751 ↗

Phase 2 Completed 168 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study was to evaluate the effect of 12 weeks of subcutaneous evolocumab (AMG 145), compared with placebo, on percent change from baseline in LDL-C in adults with heterozygous familial hypercholesterolemia (HeFH).

Timeline

Start
2011-08-02
Primary completion
2012-05-16
Completion
2012-05-16

Outcome

Met primary endpoint

registry Placebo vs Evolocumab 350 mg; p <0.001; LS Mean Treatment Difference -43.82 (95% CI -51.56 to -36.09); ANCOVA NCT01375751 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Evolocumab Monoclonal antibody 350 mg Subcutaneous
Subject Evolocumab Monoclonal antibody 420 mg Subcutaneous