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.
Medisphere Medical Research Center, Llc, Evansville, Indiana, United States
Universitätsklinikum Erlangen, Erlangen, Bavaria, Germany
UZ Leuven Gasthuisberg, Leuven, Belgium
Dana Farber Cancer Institute, Boston, Massachusetts, United States
Memorial Sloan-Kettering Cancer Center, New York, New York, United States
Sheffield Children's Hospital, Sheffield, United Kingdom
Alder Hey Children's Hospital, Liverpool, England, United Kingdom
Oxford University Hospitals - Nuffield Orthopaedic Centre, Oxford, Oxfordshire, United Kingdom
Parexel International GmbH, Early Phase Clinical Unit Berlin, Berlin, Germany
Hospital Universitario La Paz, Madrid, Madrd, Spain
Lekarna Pod Platany, Praha, Czechia
Unimed Medical Centre, Plovdiv, Bulgaria
L.K.N. Arthrocentrum, s.r.o., Hlucin, Czechia
Reade Rheumatology Research Institute, Amsterdam, Noord Holland, Netherlands
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.