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.
Reade Rheumatology Research Institute, Amsterdam, Noord Holland, Netherlands
CHRU de Besançon - Hôpital Jean Minjoz, Besançon, France
Centre hospitalier de Cholet, Cholet, Maine Et Loire, France
APHP - Hôpital du Kremlin-Bicêtre, Le Kremlin-Bicêtre, Île-de-France, France
Leeds Teaching Hospitals NHS Trust, Leeds, West Yorkshire, United Kingdom
Medical College of Wisconsin, Milwaukee, Wisconsin, United States
Connecticut Children's Medical Center, Hartford, Connecticut, United States
Nationwide Children's Hospital, Columbus, Ohio, United States
Wake Forest Health Sciences Dermatology, Winston-Salem, North Carolina, United States
Synexus (DRS) - Synexus Magyarorszag Kft. Budapest, Budapest, Hungary
Centrum Medyczne Pratia Gdynia, Gdynia, Poland
Medycyna Kliniczna Marzena Waszczak-Jeka, Warszawa, Poland
Research Site, Sussex, United Kingdom
Hôpitaux Universitaires Paris Sud - Hôpital Bicêtre, Le Kremlin Bicetre, France
Hôpital Universitaire Necker Enfants Malades, Paris, France
Centre Hospitalier Universitaire de Poitiers, Poitiers Cedex, France
The University of Michigan, Ann Arbor, Michigan, United States
Levine Children's Hospital/Atrium Health, Charlotte, North Carolina, United States
New York University, New York, New York, United States
Auckland Clinical Studies, Auckland, New Zealand
Christchurch Clinical Studies Trust Limited, Christchurch, Chistchurch, New Zealand
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