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.
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 .
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
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
Investigational Site Number 840619, Chicago, Illinois, United States
Investigational Site Number 840621, Richmond, Virginia, United States
Investigational Site Number 840602, Eugene, Oregon, United States
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