drugset / Trial / NCT02107898

Efficacy and Safety Evaluation of Alirocumab in Patients With Heterozygous Familial Hypercholesterolemia or High Cardiovascular Risk Patients With Hypercholesterolemia on Lipid Modifying Therapy (ODYSSEY JAPAN)

NCT02107898

Phase 3 Completed 216 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Primary Objective: To demonstrate the reduction of low-density lipoprotein cholesterol (LDL-C) by alirocumab as add-on therapy to stable daily statin therapy with or without other lipid modifying therapy in comparison with placebo after 24 weeks of treatment in heterozygous familial hypercholesterolemia (HeFH) or high cardiovascular risk participants with hypercholesterolemia. Secondary Objectives: * To evaluate the effect of alirocumab in comparison with placebo on LDL-C after 12 weeks of treatment. * To evaluate the effect of alirocumab on other lipid parameters. * To evaluate the long-term effect of alirocumab in comparison with placebo on LDL-C after 52 weeks of treatment. * To evaluate the safety and tolerability of alirocumab. * To evaluate the development of anti-alirocumab antibodies. * To evaluate the pharmacokinetics of alirocumab.

Timeline

Start
2014-03
Primary completion
2015-01
Completion
2015-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Alirocumab Monoclonal antibody 75 mg Subcutaneous
Subject Alirocumab Monoclonal antibody 150 mg Subcutaneous
Background Atorvastatin Small molecule
Background Fluvastatin Other / unclassified
Background Pitavastatin Small molecule
Background Pravastatin Small molecule
Background Rosuvastatin Small molecule
Background Simvastatin Small molecule

Indications