Long-term Safety and Tolerability of Alirocumab (SAR236553/REGN727) Versus Placebo on Top of Lipid-Modifying Therapy in High Cardiovascular Risk Patients With Hypercholesterolemia (ODYSSEY Long Term)

NCT ID: NCT01507831

Last Updated: 2015-12-22

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

2341 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-01-31

Study Completion Date

2014-11-30

Brief Summary

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Alirocumab (SAR236553/REGN727) is a fully human monoclonal antibody that binds PCSK9 (proprotein convertase subtilisin/kexin type 9).

Primary Objective of the study:

To evaluate the long-term safety and tolerability of alirocumab in high cardiovascular risk participants with hypercholesterolemia not adequately controlled with their current lipid modifying therapy (LMT).

Secondary Objectives:

* To evaluate the effect of alirocumab on low-density lipoprotein cholesterol (LDL-C) levels after 24 weeks of treatment in comparison with placebo.
* To evaluate the effect of alirocumab in comparison with placebo on LDL-C at other time points.
* To evaluate the effects of alirocumab on other lipid parameters.

Detailed Description

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The maximum study duration was to be 89 weeks per participant, including a 3-week screening period, a 78-week randomized treatment period and 8-week follow-up period.

Conditions

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Hypercholesterolemia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Placebo

Placebo (for alirocumab) every 2 weeks (Q2W) added to stable Lipid-Modifying Therapy (LMT) for 78 weeks.

Group Type PLACEBO_COMPARATOR

Placebo (for alirocumab)

Intervention Type DRUG

Solution for injection, one subcutaneous injection in the abdomen, thigh, or outer area of upper arm with a pre-filled syringe.

Lipid-Modifying Therapy (LMT)

Intervention Type DRUG

Statin (rosuvastatin, simvastatin or atorvastatin) at stable dose with or without other LMT as clinically indicated.

Alirocumab

Alirocumab 150 mg Q2W added to stable LMT for 78 weeks.

Group Type EXPERIMENTAL

Alirocumab

Intervention Type DRUG

Solution for injection, one subcutaneous injection in the abdomen, thigh, or outer area of upper arm with a pre-filled syringe.

Lipid-Modifying Therapy (LMT)

Intervention Type DRUG

Statin (rosuvastatin, simvastatin or atorvastatin) at stable dose with or without other LMT as clinically indicated.

Interventions

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Placebo (for alirocumab)

Solution for injection, one subcutaneous injection in the abdomen, thigh, or outer area of upper arm with a pre-filled syringe.

Intervention Type DRUG

Alirocumab

Solution for injection, one subcutaneous injection in the abdomen, thigh, or outer area of upper arm with a pre-filled syringe.

Intervention Type DRUG

Lipid-Modifying Therapy (LMT)

Statin (rosuvastatin, simvastatin or atorvastatin) at stable dose with or without other LMT as clinically indicated.

Intervention Type DRUG

Other Intervention Names

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SAR236553 REGN727 Praluent

Eligibility Criteria

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Inclusion Criteria

Either A or B below and who were not adequately controlled with their lipid-modifying therapy:

A) Participants with heterozygous familial hypercholesterolemia (heFH) with or without established coronary heart disease (CHD) or CHD risk equivalents

OR

B) Participants with hypercholesterolemia together with established CHD or CHD risk equivalents.

Exclusion Criteria

* Age \< 18 years
* LDL-C \<70 mg/dL (\< 1.81 mmol/L)
* Fasting serum triglycerides \> 400 mg/dL (\>4.52 mmol/L)

The above information was not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Regeneron Pharmaceuticals

INDUSTRY

Sponsor Role collaborator

Sanofi

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Clinical Sciences & Operations

Role: STUDY_DIRECTOR

Sanofi

Locations

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Investigational Site Number 840159

Huntsville, Alabama, United States

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Investigational Site Number 840028

Gilbert, Arizona, United States

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Investigational Site Number 840035

Sierra Vista, Arizona, United States

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Investigational Site Number 840052

Tempe, Arizona, United States

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Investigational Site Number 840065

Tempe, Arizona, United States

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Investigational Site Number 840079

Tempe, Arizona, United States

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Investigational Site Number 840094

Tempe, Arizona, United States

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Investigational Site Number 840103

Tucson, Arizona, United States

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Investigational Site Number 840209

Beverly Hills, California, United States

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Investigational Site Number 840194

Beverly Hills, California, United States

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Investigational Site Number 840207

Fresno, California, United States

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Investigational Site Number 840101

Lincoln, California, United States

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Investigational Site Number 840076

Long Beach, California, United States

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Investigational Site Number 840214

Pasadena, California, United States

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Investigational Site Number 840045

Sacramento, California, United States

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Investigational Site Number 840163

Santa Rosa, California, United States

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Investigational Site Number 840086

Colorado Springs, Colorado, United States

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Investigational Site Number 840077

Golden, Colorado, United States

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Investigational Site Number 840224

Bridgeport, Connecticut, United States

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Investigational Site Number 840134

Guilford, Connecticut, United States

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Investigational Site Number 840246

Hartford, Connecticut, United States

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Investigational Site Number 840055

Stamford, Connecticut, United States

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Investigational Site Number 840091

Stamford, Connecticut, United States

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Investigational Site Number 840150

Atlantis, Florida, United States

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Investigational Site Number 840020

Bradenton, Florida, United States

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Investigational Site Number 840041

Brandon, Florida, United States

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Investigational Site Number 840184

Clearwater, Florida, United States

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Investigational Site Number 840242

Clearwater, Florida, United States

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Investigational Site Number 840039

Clearwater, Florida, United States

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Investigational Site Number 840182

Crystal River, Florida, United States

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Investigational Site Number 840002

Daytona Beach, Florida, United States

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Investigational Site Number 840166

Daytona Beach, Florida, United States

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Investigational Site Number 840167

Fleming Island, Florida, United States

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Investigational Site Number 840090

Fort Lauderdale, Florida, United States

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Investigational Site Number 840018

Fort Lauderdale, Florida, United States

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Investigational Site Number 840153

Jacksonville, Florida, United States

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Investigational Site Number 840181

Jacksonville, Florida, United States

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Investigational Site Number 840152

Jacksonville, Florida, United States

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Investigational Site Number 840154

Lake Mary, Florida, United States

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Investigational Site Number 840059

Largo, Florida, United States

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Investigational Site Number 840221

Miami, Florida, United States

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Investigational Site Number 840021

New Port Richey, Florida, United States

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Investigational Site Number 840122

New Smyrna Beach, Florida, United States

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Investigational Site Number 840151

Ocala, Florida, United States

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Investigational Site Number 840108

Ormond Beach, Florida, United States

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Investigational Site Number 840067

Palm Harbor, Florida, United States

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Investigational Site Number 840006

Pembroke Pines, Florida, United States

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Investigational Site Number 840168

Ponte Vedra, Florida, United States

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Investigational Site Number 840164

Sarasota, Florida, United States

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Investigational Site Number 840175

Sarasota, Florida, United States

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Investigational Site Number 840001

St. Petersburg, Florida, United States

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Investigational Site Number 840003

St. Petersburg, Florida, United States

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Investigational Site Number 840036

West Palm Beach, Florida, United States

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Investigational Site Number 840117

Cumming, Georgia, United States

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Investigational Site Number 840110

Roswell, Georgia, United States

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Investigational Site Number 840026

Savannah, Georgia, United States

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Meridian, Idaho, United States

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Evansville, Indiana, United States

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Investigational Site Number 840093

Indianapolis, Indiana, United States

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Iowa City, Iowa, United States

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Investigational Site Number 840165

West Des Moines, Iowa, United States

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Kansas City, Kansas, United States

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Wichita, Kansas, United States

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Wichita, Kansas, United States

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Wichita, Kansas, United States

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Wichita, Kansas, United States

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Biddeford, Maine, United States

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Investigational Site Number 840158

Framingham, Maine, United States

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Investigational Site Number 840193

Novi, Michigan, United States

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Investigational Site Number 840162

Saginaw, Michigan, United States

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Investigational Site Number 840033

St Louis, Missouri, United States

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St Louis, Missouri, United States

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Henderson, Nevada, United States

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Henderson, Nevada, United States

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Edison, New Jersey, United States

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Hillsborough, New Jersey, United States

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Investigational Site Number 840049

Trenton, New Jersey, United States

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Bronxville, New York, United States

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Brooklyn, New York, United States

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Poughkeepsie, New York, United States

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Asheville, North Carolina, United States

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Charlotte, North Carolina, United States

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Investigational Site Number 840083

Greensboro, North Carolina, United States

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Investigational Site Number 840104

Raleigh, North Carolina, United States

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Investigational Site Number 840068

Cincinnati, Ohio, United States

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Investigational Site Number 840007

Dayton, Ohio, United States

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Investigational Site Number 840013

Marion, Ohio, United States

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Mentor, Ohio, United States

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Tulsa, Oklahoma, United States

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Beaver, Pennsylvania, United States

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Camp Hill, Pennsylvania, United States

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Duncansville, Pennsylvania, United States

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Jersey Shore, Pennsylvania, United States

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Phoenixville, Pennsylvania, United States

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Scranton, Pennsylvania, United States

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Wyomissing, Pennsylvania, United States

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Charleston, South Carolina, United States

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Greenville, South Carolina, United States

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Simpsonville, South Carolina, United States

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Investigational Site Number 840105

Varnville, South Carolina, United States

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Knoxville, Tennessee, United States

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Dallas, Texas, United States

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Dallas, Texas, United States

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Fort Worth, Texas, United States

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Investigational Site Number 840149

Fort Worth, Texas, United States

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Fort Worth, Texas, United States

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Houston, Texas, United States

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Houston, Texas, United States

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Plano, Texas, United States

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Sugar Land, Texas, United States

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Tyler, Texas, United States

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Salt Lake City, Utah, United States

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Chesapeake, Virginia, United States

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Spokane, Washington, United States

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Milwaukee, Wisconsin, United States

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Investigational Site Number 032006

Buenos Aires, , Argentina

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Caba, , Argentina

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Capital Federal, , Argentina

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Coronel Suárez, , Argentina

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Resistencia, , Argentina

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Zárate, , Argentina

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Antwerp, , Belgium

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Genk, , Belgium

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Natoye, , Belgium

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Wetteren, , Belgium

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Pleven, , Bulgaria

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Plovdiv, , Bulgaria

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Sofia, , Bulgaria

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Sofia, , Bulgaria

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Sofia, , Bulgaria

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Sofia, , Bulgaria

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Sofia, , Bulgaria

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Stara Zagora, , Bulgaria

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Varna, , Bulgaria

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Cambridge, , Canada

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Coquitlam, , Canada

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Hawkesbury, , Canada

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London, , Canada

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Mirabel, , Canada

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Montreal, , Canada

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Ottawa, , Canada

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Québec, , Canada

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Sarnia, , Canada

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St. John's, , Canada

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Terrebonne, , Canada

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Vancouver, , Canada

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Victoria, , Canada

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Woodstock, , Canada

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Osorno, , Chile

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Santiago, , Chile

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Santiago, , Chile

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Temuco, , Chile

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Barranquilla, , Colombia

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Barranquilla, , Colombia

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Barranquilla, , Colombia

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Manizales, , Colombia

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Medellín, , Colombia

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Prague, , Czechia

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Prague, , Czechia

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Prague, , Czechia

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Aarhus, , Denmark

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Hellerup, , Denmark

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Slagelse, , Denmark

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Svendborg, , Denmark

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Viborg, , Denmark

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Joensuu, , Finland

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Kokkola, , Finland

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Kuopio, , Finland

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Vantaa, , Finland

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Bandol, , France

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Broglie, , France

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Bron, , France

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Dijon, , France

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Lille, , France

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Nantes, , France

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Nantes, , France

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Paris, , France

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Pessac, , France

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Rennes, , France

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Vieux-Condé, , France

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Vihiers, , France

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Investigational Site Number 276001

Bad Wörishofen, , Germany

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Berlin, , Germany

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Berlin, , Germany

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Berlin, , Germany

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Bochum, , Germany

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Dresden, , Germany

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Essen, , Germany

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Frankfurt A.M., , Germany

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Görlitz, , Germany

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Investigational Site Number 276019

Hanover, , Germany

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Leipzig, , Germany

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Magdeburg, , Germany

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Investigational Site Number 276003

Magdeburg, , Germany

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Investigational Site Number 276006

Schwerin, , Germany

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Witten, , Germany

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Investigational Site Number 348003

Baja, , Hungary

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Investigational Site Number 348007

Budapest, , Hungary

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Investigational Site Number 348009

Budapest, , Hungary

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Investigational Site Number 348008

Budapest, , Hungary

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Budapest, , Hungary

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Debrecen, , Hungary

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Nagykanizsa, , Hungary

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Nyíregyháza, , Hungary

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Sopron, , Hungary

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Úrhida, , Hungary

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Investigational Site Number 376002

Afula, , Israel

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Holon, , Israel

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Holon, , Israel

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Nazareth, , Israel

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Chieti, , Italy

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Cinisello Balsamo, , Italy

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Milan, , Italy

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Napoli, , Italy

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Palermo, , Italy

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Pozzilli, , Italy

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Vittorio Veneto, , Italy

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Zingonia-Osio Sotto, , Italy

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Df, , Mexico

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México, , Mexico

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Not Provided, , Mexico

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San Luis Potosí City, , Mexico

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Tijuana, , Mexico

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Torreón, , Mexico

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Xalapa, , Mexico

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Amsterdam, , Netherlands

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Amsterdam, , Netherlands

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Breda, , Netherlands

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Eindhoven, , Netherlands

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Groningen, , Netherlands

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Hoogeveen, , Netherlands

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Hoorn, , Netherlands

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Leiderdorp, , Netherlands

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Rotterdam, , Netherlands

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Velp, , Netherlands

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Venlo, , Netherlands

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Zoetermeer, , Netherlands

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Elverum, , Norway

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Hamar, , Norway

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Oslo, , Norway

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Skedsmokorset, , Norway

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Stavanger, , Norway

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Gdynia, , Poland

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Gdynia, , Poland

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Gniewkowo, , Poland

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Katowice, , Poland

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Krakow, , Poland

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Piotrkow Trybunalski, , Poland

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Puławy, , Poland

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Warsaw, , Poland

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Wroclaw, , Poland

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Funchal / Madeira, , Portugal

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Lisbon, , Portugal

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Lisbon, , Portugal

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Porto, , Portugal

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Baia Mare, , Romania

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Brasov, , Romania

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Târgu Mureş, , Romania

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Timișoara, , Romania

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Barnaul, , Russia

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Moscow, , Russia

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Moscow, , Russia

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Perm, , Russia

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Saint Petersburg, , Russia

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Saint Petersburg, , Russia

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Yaroslavl, , Russia

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Centurion, , South Africa

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Meyerspark, , South Africa

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Middelburg, , South Africa

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Parktown, , South Africa

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Pretoria, , South Africa

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Pretoria, , South Africa

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Pretoria, , South Africa

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Roodepoort, , South Africa

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Somerset West, , South Africa

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Witbank, , South Africa

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Worcester, , South Africa

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Córdoba, , Spain

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Granada, , Spain

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Madrid, , Spain

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Málaga, , Spain

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Quart de Poblet, , Spain

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Reus, , Spain

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Sabadell, , Spain

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Seville, , Spain

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Örebro, , Sweden

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Rättvik, , Sweden

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Stockholm, , Sweden

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Stockholm, , Sweden

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Stockholm, , Sweden

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Chernivtsi, , Ukraine

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Dnipropetrovsk, , Ukraine

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Donetsk, , Ukraine

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Kharkiv, , Ukraine

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Kiev, , Ukraine

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Kyiv, , Ukraine

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Kyiv, , Ukraine

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Kyiv, , Ukraine

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Kyiv, , Ukraine

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Kyiv, , Ukraine

Site Status

Investigational Site Number 804005

Zhytomyr, , Ukraine

Site Status

Investigational Site Number 826004

Addlestone, , United Kingdom

Site Status

Investigational Site Number 826009

Birmingham, , United Kingdom

Site Status

Investigational Site Number 826016

Birmingham, , United Kingdom

Site Status

Investigational Site Number 826021

Blackpool, , United Kingdom

Site Status

Investigational Site Number 826023

Cambridge, , United Kingdom

Site Status

Investigational Site Number 826012

Cardiff, , United Kingdom

Site Status

Investigational Site Number 826024

Chichester, , United Kingdom

Site Status

Investigational Site Number 826006

Chorley, , United Kingdom

Site Status

Investigational Site Number 826010

Glasgow, , United Kingdom

Site Status

Investigational Site Number 826003

Irvine, , United Kingdom

Site Status

Investigational Site Number 826008

Liverpool, , United Kingdom

Site Status

Investigational Site Number 826005

Liverpool, , United Kingdom

Site Status

Investigational Site Number 826025

Manchester, , United Kingdom

Site Status

Investigational Site Number 826007

Manchester, , United Kingdom

Site Status

Investigational Site Number 826001

Middlesex, , United Kingdom

Site Status

Investigational Site Number 826019

Penzance, , United Kingdom

Site Status

Investigational Site Number 826011

Reading, , United Kingdom

Site Status

Investigational Site Number 826013

Romford, , United Kingdom

Site Status

Investigational Site Number 826014

Soham, , United Kingdom

Site Status

Countries

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United States Argentina Belgium Bulgaria Canada Chile Colombia Czechia Denmark Finland France Germany Hungary Israel Italy Mexico Netherlands Norway Poland Portugal Romania Russia South Africa Spain Sweden Ukraine United Kingdom

References

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Robinson JG, Farnier M, Krempf M, Bergeron J, Luc G, Averna M, Stroes ES, Langslet G, Raal FJ, El Shahawy M, Koren MJ, Lepor NE, Lorenzato C, Pordy R, Chaudhari U, Kastelein JJ; ODYSSEY LONG TERM Investigators. Efficacy and safety of alirocumab in reducing lipids and cardiovascular events. N Engl J Med. 2015 Apr 16;372(16):1489-99. doi: 10.1056/NEJMoa1501031. Epub 2015 Mar 15.

Reference Type RESULT
PMID: 25773378 (View on PubMed)

Mahmood T, Minnier J, Ito MK, Li QH, Koren A, Kam IW, Fazio S, Shapiro MD. Discordant responses of plasma low-density lipoprotein cholesterol and lipoprotein(a) to alirocumab: A pooled analysis from 10 ODYSSEY Phase 3 studies. Eur J Prev Cardiol. 2021 Jul 23;28(8):816-822. doi: 10.1177/2047487320915803. Epub 2020 Apr 10.

Reference Type DERIVED
PMID: 34298554 (View on PubMed)

Leiter LA, Tinahones FJ, Karalis DG, Bujas-Bobanovic M, Letierce A, Mandel J, Samuel R, Jones PH. Alirocumab safety in people with and without diabetes mellitus: pooled data from 14 ODYSSEY trials. Diabet Med. 2018 Dec;35(12):1742-1751. doi: 10.1111/dme.13817. Epub 2018 Oct 9.

Reference Type DERIVED
PMID: 30183102 (View on PubMed)

Defesche JC, Stefanutti C, Langslet G, Hopkins PN, Seiz W, Baccara-Dinet MT, Hamon SC, Banerjee P, Kastelein JJP. Efficacy of alirocumab in 1191 patients with a wide spectrum of mutations in genes causative for familial hypercholesterolemia. J Clin Lipidol. 2017 Nov-Dec;11(6):1338-1346.e7. doi: 10.1016/j.jacl.2017.08.016. Epub 2017 Sep 4.

Reference Type DERIVED
PMID: 28964736 (View on PubMed)

Kastelein JJ, Hovingh GK, Langslet G, Baccara-Dinet MT, Gipe DA, Chaudhari U, Zhao J, Minini P, Farnier M. Efficacy and safety of the proprotein convertase subtilisin/kexin type 9 monoclonal antibody alirocumab vs placebo in patients with heterozygous familial hypercholesterolemia. J Clin Lipidol. 2017 Jan-Feb;11(1):195-203.e4. doi: 10.1016/j.jacl.2016.12.004. Epub 2016 Dec 28.

Reference Type DERIVED
PMID: 28391886 (View on PubMed)

Ray KK, Ginsberg HN, Davidson MH, Pordy R, Bessac L, Minini P, Eckel RH, Cannon CP. Reductions in Atherogenic Lipids and Major Cardiovascular Events: A Pooled Analysis of 10 ODYSSEY Trials Comparing Alirocumab With Control. Circulation. 2016 Dec 13;134(24):1931-1943. doi: 10.1161/CIRCULATIONAHA.116.024604. Epub 2016 Oct 24.

Reference Type DERIVED
PMID: 27777279 (View on PubMed)

Other Identifiers

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2011-002806-59

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

U1111-1121-3928

Identifier Type: OTHER

Identifier Source: secondary_id

LTS11717

Identifier Type: -

Identifier Source: org_study_id