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.
Federal State Budgetary Educational Institution of Higher Education "Altai State Medical University" of the Ministry of Health of the Russian Federation, Barnaul, Russian Federation
State budgetary healthcare institution "Chelyabinsk Regional Clinical Dermatovenerological Dispensary", Chelyabinsk, Russian Federation
State budgetary institution of the Sverdlovsk region "Ural Research Institute of Dermatovenereology and Immunopathology", Ekaterinburg, Russian Federation
Novartis Pharma K.K., Tokyo, Japan
Rheumatology Section, University of Verona, Verona, Italy
Zhongshan Hospital, Fudan University, Shanghai, Shanghai, China
South Valley Hospitals, Qinā, Egypt
Västra Götalandsregionen, Göteborg, Sweden
Centrum Medyczne Melita Medical /ID# 258379, Wrocław, Dolnoslaskie, Poland
Centrum Medyczne LukaMed Joanna Luka /ID# 258457, Chojnice, Pomorskie, Poland
Caribbean Medical Research Center /ID# 268395, San Juan, Puerto Rico
Site 01, Beijing, Beijing, China
APHP - Hôpital Bicêtre, Le Kremlin-Bicêtre, Paris, France
CHU Amiens, Amiens, France
CHRU Lille, Lille, France
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