drugset / Trial / NCT01709513

Study of Alirocumab (REGN727/SAR236553) in Patients With Primary Hypercholesterolemia and Moderate, High, or Very High Cardiovascular (CV) Risk, Who Are Intolerant to Statins (ODYSSEY ALTERNATIVE)

NCT01709513 ↗

Phase 3 Completed 314 enrolled Regeneron Pharmaceuticals Sanofi · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-blind, double-dummy, active-controlled, parallel-group, multi-national, multi-center study to compare alirocumab (REGN727/SAR236553) versus ezetimibe in participants with primary hypercholesterolemia and moderate, high, or very high CV risk, who are intolerant to statins. An atorvastatin arm is added to determine that the population selected in the study is a truly statin intolerant population by assessing skeletal muscle-related adverse events.

Timeline

Start
2012-09-30
Primary completion
2014-05-31
Completion
2017-05-31

Outcome

Met primary endpoint

paper Alirocumab reduced mean (standard error) LDL-C by 45.0% (2.2%) vs 14.6% (2.2%) with ezetimibe (mean difference 30.4% [3.1%], P < .0001). PMID 26687696 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Alirocumab Monoclonal antibody 75 mg Subcutaneous
Subject Alirocumab Monoclonal antibody 150 mg Subcutaneous
Subject Atorvastatin Small molecule 20 mg Oral
Comparator Ezetimibe Unknown 10 mg Oral

Indications