drugset / Trial / NCT01709500

Study of Alirocumab (REGN727/SAR236553) in Patients With heFH (Heterozygous Familial Hypercholesterolemia) Who Are Not Adequately Controlled With Their LMT (Lipid-Modifying Therapy)

NCT01709500 ↗

Phase 3 Completed 249 enrolled Regeneron Pharmaceuticals Sanofi · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled, parallel-group, multi-national study alirocumab (REGN727/SAR236553) in patients with Heterozygous Familial Hypercholesterolemia (heFH) who are not adequately controlled with their Lipid-Modifying Therapy (LMT).

Timeline

Start
2012-12
Primary completion
2014-05
Completion
2015-01

Outcome

Met primary endpoint

registry Alirocumab 75 mg/up to 150 mg vs Placebo; p <0.0001; LS Mean Difference -51.4 (95% CI -58.1 to -44.8) NCT01709500 ↗

paper At week 24, alirocumab reduced LDL-C levels by -48.8% (75/150 mg Q2W; placebo: +7.1%) PMID 28391886 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Alirocumab Monoclonal antibody 75 mg Subcutaneous
Subject Alirocumab Monoclonal antibody 150 mg Subcutaneous
Background Atorvastatin Small molecule — —
Background Rosuvastatin Small molecule — —
Background Simvastatin Small molecule — —