MedPath

Alirocumab

Generic Name
Alirocumab
Brand Names
Praluent
Drug Type
Biotech
CAS Number
1245916-14-6
Unique Ingredient Identifier
PP0SHH6V16
Background

Alirocumab is a biopharmaceutical that obtained FDA approval in July 2015 as a second line treatment for high cholesterol in adults whose LDL-cholesterol (LDL-C) is not controlled by the combination of diet and statin treatment. It is a human monoclonal antibody part of the family of the PCSK9 inhibitors which are a novel class of anticholesterol therapeutics. From this family, it was the first agent to receive FDA approval. The FDA approval was contingent on the completion of further clinical trials to better determine efficacy and safety. PCSK9 inhibition facilitates more LDL-C clearance from the blood.

Indication

Alirocumab is an antibody eliciting proprotein convertase subtilisin kexin type 9 (PCSK9) inhibitor activity that is indicated for:

(i) use in reducing the risk of myocardial infarction, stroke, and unstable angina requiring hospitalization in adults with established cardiovascular disease , and/or

(ii) use as an adjunct to diet or use alone or in combination with other lipid-lowering therapies (statins, ezetimibe, for example) for the treatment of adults with primary hyperlipidemia (including heterozygous familial hypercholesterolemia) to reduce low-density lipoprotein cholesterol (LDL-C) levels in the body .

Associated Conditions
Heterozygous Familial Hypercholesterolemia (HeFH), Homozygous Familial Hypercholesterolaemia (HoFH), Myocardial Infarction, Stroke, Unstable Angina Pectoris, Primary Hyperlipidemia

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)

Phase 3
Completed
Conditions
Hypercholesterolemia
Interventions
Drug: Placebo (for alirocumab)
Drug: Lipid-Modifying Therapy (LMT)
First Posted Date
2012-01-11
Last Posted Date
2015-12-22
Lead Sponsor
Sanofi
Target Recruit Count
2341
Registration Number
NCT01507831
Locations
🇺🇸

Investigational Site Number 840047, Houston, Texas, United States

🇺🇸

Investigational Site Number 840076, Long Beach, California, United States

🇺🇸

Investigational Site Number 840163, Santa Rosa, California, United States

and more 317 locations

Injection Site Tolerability, Safety, Pharmacokinetics and Pharmacodynamics Study After a Single Dose Subcutaneous Treatment of Alirocumab SAR236553 (REGN727)

Phase 1
Completed
Conditions
Hypercholesterolemia
Interventions
First Posted Date
2011-10-07
Last Posted Date
2013-06-28
Lead Sponsor
Sanofi
Target Recruit Count
24
Registration Number
NCT01448239
Locations
🇺🇸

Sanofi-Aventis Administrative Office, Bridgewater, New Jersey, United States

Study of the Tolerability, Safety, Pharmacokinetics and Pharmacodynamics of Alirocumab SAR236553 (REGN727)

Phase 1
Completed
Conditions
Hypercholesterolemia
Interventions
First Posted Date
2011-10-07
Last Posted Date
2013-06-28
Lead Sponsor
Sanofi
Target Recruit Count
24
Registration Number
NCT01448304
Locations
🇺🇸

Sanofi-Aventis Administrative Office, Bridgewater, New Jersey, United States

Ascending Dose Study of the Safety and Tolerability of Alirocumab (SAR236553/REGN727) in Japanese Healthy Volunteers

Phase 1
Completed
Conditions
Hypercholesterolemia
Interventions
Drug: Placebo (Lyophilized formulation)
Drug: Placebo (Solution)
First Posted Date
2011-10-07
Last Posted Date
2016-09-28
Lead Sponsor
Sanofi
Target Recruit Count
32
Registration Number
NCT01448317
Locations
🇯🇵

Sanofi-Aventis Administrative Office, Tokyo, Japan

Injection Site Tolerability, Safety, Pharmacokinetics, Pharmacodynamics in Different Single-Dose Treatments of Alirocumab SAR236553 (REGN727) in Healthy Subjects

Phase 1
Completed
Conditions
Hypercholesterolemia
Interventions
First Posted Date
2011-09-30
Last Posted Date
2013-06-28
Lead Sponsor
Sanofi
Target Recruit Count
36
Registration Number
NCT01443650
Locations
🇺🇸

Sanofi-Aventis Administrative Office, Bridgewater, New Jersey, United States

Efficacy and Safety Evaluation of Alirocumab (SAR236553/REGN727) When Co-administered With High Dose of Atorvastatin in Patients With Primary Hypercholesterolemia

Phase 2
Completed
Conditions
Hypercholesterolemia
Interventions
Drug: Placebo (for alirocumab)
Drug: Placebo (for atorvastatin)
First Posted Date
2011-02-02
Last Posted Date
2015-09-24
Lead Sponsor
Sanofi
Target Recruit Count
92
Registration Number
NCT01288469
Locations
🇺🇸

Investigational Site Number 840619, Chicago, Illinois, United States

🇺🇸

Investigational Site Number 840621, Richmond, Virginia, United States

🇺🇸

Investigational Site Number 840602, Eugene, Oregon, United States

and more 17 locations

Efficacy and Safety Evaluation of Alirocumab (SAR236553/REGN727) in Patients With Primary Hypercholesterolemia on Stable Atorvastatin Therapy

Phase 2
Completed
Conditions
Hypercholesterolemia
Interventions
Drug: Placebo (for alirocumab)
First Posted Date
2011-02-02
Last Posted Date
2015-09-24
Lead Sponsor
Sanofi
Target Recruit Count
183
Registration Number
NCT01288443
Locations
🇺🇸

Investigational Site Number 840525, Tempe, Arizona, United States

🇺🇸

Investigational Site Number 840521, Bristol, Tennessee, United States

🇺🇸

Investigational Site Number 840516, Los Angeles, California, United States

and more 35 locations

Study of the Safety and Efficacy of REGN727/SAR236553 in Patients With HeFH Hypercholesterolemia

Phase 2
Completed
Conditions
Hypercholesterolemia
Interventions
Drug: Placebo
First Posted Date
2010-12-24
Last Posted Date
2015-09-22
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
77
Registration Number
NCT01266876

Ascending Dose Study of the Safety and Tolerability of REGN727 (SAR236553) in Healthy Volunteers

Phase 1
Completed
Conditions
Healthy Volunteers
Interventions
Drug: Placebo
First Posted Date
2010-02-24
Last Posted Date
2015-01-27
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
32
Registration Number
NCT01074372

Ascending Dose Study of the Safety and Tolerability of REGN727(SAR236553) in Healthy Volunteers

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: Placebo
First Posted Date
2009-12-04
Last Posted Date
2015-01-27
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
40
Registration Number
NCT01026597
© Copyright 2025. All Rights Reserved by MedPath