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.
Servicio de Oftalmologia. Hospital Universitario Vall d'Hebron, Barcelona, Spain
Dep. of Rheumatology, Glostrup Hospital, Copenhagen, Denmark
Dep. of medicine, Herlev Hospital, Copenhagen, Denmark
Dep. of Radiology, Herlev Hospital, Copenhagen, Denmark
Dep. of Rheumatologym Glostrup Hospital, Copenhagen, Denmark
Dep. of Rheumatology, Helsinør Hospital, Hørsholm, Denmark
Dep. of Radiology, Herlev Hospital, Copenhagen, Denmark
Laureate Clinical Research Group, Atlanta, Georgia, United States
Mountain State Clinical Research, Clarksburg, West Virginia, United States
Arthritis And Rheumatic Disease Specialties, Aventura, Florida, United States
Rafic Hariri University Hospital, Beirut, South Beirut, Lebanon
University of Alabama, Birmingham, Alabama, United States
University of Rochester, Rochester, New York, United States
University of California, San Francisco, San Francisco, California, United States
Centre de Recherche Clinique Ethienne Lebel, Fleurimont, Quebec, Canada
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