Fremanezumab is a humanized monoclonal antibody targeted against human calcitonin gene-related peptide (CGRP) for the prevention of migraine headaches. It was developed by Teva Pharmaceuticals USA and approved by the FDA in September 2018. Along with other recently approved anti-CGRP therapies such as galcanezumab, erenumab, and the oral CGRP antagonist ubrogepant, fremanezumab represents an important step forward in the treatment and prevention of migraine headaches.
Fremanezumab is indicated for the preventative treatment of migraine in adults.
Department of Neurology, Inselspital, Bern, Switzerland
Hospital Clínico Universitario de Valladolid, Valladolid, Spain
Cleveland Clinic, Main Campus, Cleveland, Ohio, United States
Brigham and Women's Health Care Center, Chestnut Hill, Massachusetts, United States
Teva Investigational Site 88022, Changsha Shi, China
Teva Investigational Site 88015, Suzhou Shi, China
Teva Investigational Site 88023, Tianjin Shi, China
Pharmacovigilance Department, Osaka, Japan
Gilbert Neurology Partners/ CCT Research, Gilbert, Arizona, United States
Ki Clinical Research LLC, dba New England Institute for Clinical Research, Stamford, Connecticut, United States
Innovation Medical Group, Palmetto Bay, Florida, United States
Medical University Innsbruck, Innsbruck, Tirol, Austria
Clinic Hietzing, Vienna, Austria
Medizinische Universität Wien, Wien, Vienna, Austria
BIDMC Headaceh Clinic, Boston, Massachusetts, United States
Medical University of Vienna, Vienna, Austria
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