Completed

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)

Clinicaltrials.gov Identifier: 

nct02107898

Trial details

Trial date:
March 2014 - January 2015
Phase:  3
Birth sex
Male and female gender symbols.
Age range
20 Years to 80 Years
Accepts healthy volunteers
No
Condition(s) being studied: 

Hypercholesterolemia

What is the type of trial? 

Interventional

What is the trial testing? 

Alirocumab, Lipid-Modifying Therapy (LMT), Placebo (for alirocumab)

How many people are being enrolled? 

216

Trial 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.

Trial locations

location(s)