drugset / Trial / NCT02392559

Trial Assessing Efficacy, Safety and Tolerability of Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Inhibition in Paediatric Subjects With Genetic Low-Density Lipoprotein (LDL) Disorders

NCT02392559 ↗

Phase 3 Completed 158 enrolled Amgen
RandomizedParallel-groupTriple-blindTreatment

Summary

A study to assess safety and efficacy of evolocumab (AMG-145) in paediatric subjects aged 10-17 years diagnosed with heterozygous familial hypercholesterolemia.

Timeline

Start
2016-03-24
Primary completion
2019-11-25
Completion
2019-11-25

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs EvoMab 420 mg QM; p < 0.0001; treatment difference -38.30 (95% CI -45.54 to -31.06); repeated measures model NCT02392559 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Evolocumab Monoclonal antibody 420 mg Subcutaneous