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.
Institute of Rheumatic & Musculoskeletal Medicine, Chapel Allerton Hospital, Leeds, West Yorkshire, United Kingdom
Saitama Medical Center, Kawagoe, Saitama, Japan
Keio University Hospital, Shinanomachi, Tokyo, Japan
Department of Rheumatology, Skåne University Hospital, Malmö, Sweden
Site Ref # / Investigator 17682, Kazan, Russian Federation
Site Ref # / Investigator 18081, Saint Petersburg, Russian Federation
Site Ref # / Investigator 17681, Moscow, Russian Federation
Dep of Rheumatology, Stockholm, Sweden
MR Centre, Dep of Clinical Neuroscience, Stockholm, Sweden
Innovaderm Research Inc., Montreal, Quebec, Canada
Regional Hospital of Silkeborg, Silkeborg, Denmark
Department of Rheumatology U, Aarhus Hospital, Aarhus, Denmark
Regional Hospital of Horsens, Department of Medicine, Horsens, Denmark
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