drugset / Trial / NCT01644188

Efficacy and Safety of Alirocumab (SAR236553/REGN727) Versus Ezetimibe on Top of Statin in High Cardiovascular Risk Patients With Hypercholesterolemia (ODYSSEY COMBO II)

NCT01644188 ↗

Phase 3 Completed 720 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Alirocumab (SAR236553/REGN727) is a fully human monoclonal antibody that binds PCSK9 (proprotein convertase subtilisin/kexin type 9). Primary Objective of the study: To demonstrate the reduction of low-density lipoprotein cholesterol (LDL-C) by alirocumab as add-on therapy to stable maximally tolerated daily statin therapy in comparison with ezetimibe after 24 weeks of treatment in participants with hypercholesterolemia at high cardiovascular (CV) risk. Secondary Objectives: * To evaluate the effect of alirocumab in comparison with ezetimibe on LDL-C at other time points * To evaluate the effect of alirocumab on other lipid parameters * To evaluate the safety and tolerability of alirocumab

Timeline

Start
2012-08
Primary completion
2014-05
Completion
2015-07

Outcome

Met primary endpoint

paper 50.6 ± 1.4% for alirocumab vs. 20.7 ± 1.9% for ezetimibe (difference 29.8 ± 2.3%; P < 0.0001) PMID 25687353 ↗

registry analysis (superiority or other test); Alirocumab 75 /up to 150 mg Q2W vs Ezetimibe 10 mg; p <0.0001; LS Mean Difference -29.8 (95% CI -34.4 to -25.3); NCT01644188 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Alirocumab Monoclonal antibody 75 mg Subcutaneous
Subject Alirocumab Monoclonal antibody 150 mg Subcutaneous
Comparator Ezetimibe Unknown 10 mg Oral
Background Atorvastatin Small molecule — —
Background Rosuvastatin Small molecule — —
Background Simvastatin Small molecule — —

Indications