Erenumab (AMG-334) (INN; trade name Aimovig) is a human monoclonal antibody designed specifically to bind and antagonize the calcitonin gene-related peptide receptor (CGRPR) as a means to prevent migraines. Aimovig, as released and marketed by Novartis and Amgen, is in fact a novel therapeutic approach as the first and only FDA approved treatment specifically developed to prevent migraine by blocking the CGRP receptor, which is believed to play a critical role in migraine .
In particular, erenumab-aooe is a human immunoglobulin G2 monoclonal antibody that has high affinity binding to the CGRP receptor . The antibody is produced utlilizing recombinant DNA technology in Chinese hamster ovary cells . It is composed of 2 heavy chains, each containing 456 amino acids, and 2 light chains of the lambda subclass, each containing 216 amino acids, with an approximate molecular weight of 150 kDa .
Erenumab is indicated for the preventative treatment of migraine in adults .
Phoenix VA Health Care System, Phoenix, Arizona, United States
Mayo Clinic, Rochester, Minnesota, United States
Mayo Clinic in Arizona, Scottsdale, Arizona, United States
Novartis Investigative Site, Wuerzburg, Germany
Danish Headache Center, Department of Neurology, Rigshospitalet - Glostrup, Glostrup, Denmark
Novartis Investigative Site, Napoli, Italy
Research Site, Salt Lake City, Utah, United States
Paradigm Clinical Research Center Inc, San Diego, California, United States
Childrens Hospital Colorado, Aurora, Colorado, United States
Colorado Springs Neurological Associates, Colorado Springs, Colorado, United States
Research Site, Kai-shi, Yamanashi, Japan
Mayo Clinic in Arizona, Scottsdale, Arizona, United States
Research Site, Madison, Wisconsin, United States
Research Site, Leuven, Belgium
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.