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 ubro...
Fremanezumab is indicated for the preventative treatment of migraine in adults.
Teva Investigational Site 32734, Leipzig, Germany
Teva Investigational Site 63075, Athens, Greece
Teva Investigational Site 14337, San Diego, California, United States
Teva Investigational Site 14179, Dallas, Texas, United States
Teva Investigational Site 14431, Mesa, Arizona, United States
Teva Investigational Site 14164, San Diego, California, United States
Teva Investigational Site 14119, Albany, New York, United States
Teva Investigational Site 14055, Dallas, Texas, United States
Teva Investigational Site 14064, Philadelphia, Pennsylvania, United States
Teva Investigational Site 14760, Decatur, Georgia, United States
Teva Investigational Site 14739, San Diego, California, United States
Teva Investigational Site 42054, Stockholm, Sweden
Teva Investigational Site 13812, Stamford, Connecticut, United States
Teva Investigational Site 13809, Raleigh, North Carolina, United States
Teva Investigational Site 13824, Philadelphia, Pennsylvania, United States
Teva Investigational Site 13813, Englewood, Colorado, United States
Teva Investigational Site 13820, Princeton, New Jersey, United States
Teva Investigational Site 13824, Philadelphia, Pennsylvania, United States
Teva Investigational Site 13834, Phoenix, Arizona, United States
Teva Investigational Site 13819, Canoga Park, California, United States
Teva Investigational Site 13811, Santa Monica, California, United States
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