drugset / Trial / NCT02584504

Efficacy and Safety of Alirocumab in Patients With Hypercholesterolemia Not Adequately Controlled With Non-statin Lipid Modifying Therapy or the Lowest Strength of Statin

NCT02584504

Phase 3 Completed 163 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Primary Objective: To demonstrate the reduction of low-density lipoprotein cholesterol (LDL-C) by alirocumab administration as add-on therapy to non-statin lipid modifying therapy (LMT) including diet therapy alone or the lowest strength of statin in comparison with placebo after 12 weeks of treatment in participants with hypercholesterolemia. Secondary Objective: * To evaluate the effect of two treatment regimens of alirocumab on other lipid parameters: apolipoprotein B (Apo-B), non-high-density lipoprotein cholesterol (non HDL-C), total cholesterol (TC), lipoprotein (a) (Lp\[a\]), high-density lipoprotein cholesterol (HDL-C), triglyceride (TG), and apolipoprotein A-1 (Apo A-1). * To evaluate the safety and tolerability of alirocumab administration. * To evaluate the development of anti-alirocumab antibodies. * To evaluate the pharmacokinetic and pharmacodynamic profiles of alirocumab administration. * To evaluate the long-term safety in participants receiving open-label alirocumab administration.

Timeline

Start
2015-11-30
Primary completion
2017-04-05
Completion
2018-01-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Alirocumab Monoclonal antibody 150 mg Subcutaneous
Background Atorvastatin Small molecule 5 mg Oral
Background Bezafibrate Small molecule
Background Ezetimibe Unknown
Background Fenofibrate Small molecule

Indications