Adalimumab is a subcutaneously administered biological disease modifier for the treatment of rheumatoid arthritis and other chronic debilitating diseases mediated by tumor necrosis factor. It was originally launched by Abbvie in the U.S. and approved in 2002 by the FDA. This drug is frequently known as Humira. It is produced by recombinant DNA technology usi...
Adalimumab is indicated for the following conditions:
Adalimumab has also been used off-label to treat Pyoderma gangrenosum.
University of Michigan, Ann Arbor, Michigan, United States
Children's Mercy Hospital, Kansas City, Missouri, United States
Cardinal Glennon Children's Medical Center, Saint Louis, Missouri, United States
Stanford University, Palo Alto, California, United States
Altoona Center for Clinical Research, Duncansville, Pennsylvania, United States
Feinstein Institute for Medical Research NS-LIJ, Manhassett, New York, United States
LUMC, Leiden, Netherlands
St Antonius ziekenhuis, Nieuwegein, Netherlands
UMC Radboud, Nijmegen, Netherlands
Wake Forest University Health Sciences Dermatology, Winston-Salem, North Carolina, United States
Wake Forest University Health Sciences Dermatology, Winston-Salem, North Carolina, United States
The University of Alberta Hospital, Edmonton, Alberta, Canada
Aarhus University Hospital, Aarhus, Denmark
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