drugset / Trial / NCT01588496

Trial Evaluating PCSK9 Antibody in Subjects With LDL Receptor Abnormalities

NCT01588496 ↗

Phase 2/3 Completed 58 enrolled Amgen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A study to determine the safety, tolerability, and efficacy of evolocumab (AMG 145) in patients with homozygous familial hypercholesterolemia (HoFH).

Timeline

Start
2012-04-05
Primary completion
2014-01-31
Completion
2014-01-31

Outcome

Met primary endpoint

paper Compared with placebo, evolocumab significantly reduced ultracentrifugation LDL cholesterol at 12 weeks by 30·9% (95% CI -43·9% to -18·0%; p<0·0001). PMID 25282520 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Evolocumab Monoclonal antibody 420 mg Subcutaneous