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Summary
April 2007, Vol. 8, No. 6, Pages 831-838
, DOI 10.1517/14656566.8.6.831
Adalimumab for the treatment of ankylosing spondylitisJoachim Sieper1Professor, Campus Benjamin Franklin, Rheumatology, Medical Department I,Charité, Hindenburgdamm 30, 12200 Berlin, Germany. joachim.sieper@charite.de 2Doctor, Campus Benjamin Franklin, Rheumatology, Medical Department I,Charité, Hindenburgdamm 30, 12200 Berlin, Germany 3Professor, Rheumazentrum Ruhrgebiet, Herne, Germany Ankylosing spondylitis is a chronic inflammatory disease, with a prevalence of Forward Links to Citing ArticlesW. Ebner, T. Palotai, C. Codreanu, P. Géher, A. Pahor, K. Pavelka, J. Smolen, J. Szechiński, M. Žlnay. (2008) Ankylosierende Spondylitis in Mittel- und Osteuropa. Zeitschrift für Rheumatologie 67:6, 503-510 Online publication date: 1-Nov-2008. CrossRef Pascal Juillerat, Christian Mottet, Valérie Pittet, Florian Froehlich, Christian Felley, Jean-Jacques Gonvers, John-Paul Vader, Pierre Michetti. (2007) Extraintestinal Manifestations of Crohn’s Disease. Digestion 76:2, 141-148 Online publication date: 1-Feb-2007. CrossRef |
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0.5%, which starts in the third decade of life. Treatment was, until recently, limited. Conventional disease-modifying drugs are not effective for the spinal manifestations, and NSAIDs and physical therapy were the standard treatment, without any other options for patients who did not respond to this treatment. Therefore, the high efficacy of the new group of TNF-blockers for the treatment of active ankylosing spondylitis represents a breakthrough for NSAID-refractory patients. Following the introduction of the two TNF-blockers, infliximab and etanercept, the fully humanized, anti-TNF monoclonal antibody adalimumab is now the third product that has been approved for the treatment of ankylosing spondylitis. Adalimumab is given subcutaneously every 2 weeks at a dose of 40 mg. In open and placebo-controlled trials, the drug was shown to be safe and effective in ankylosing spondylitis patients. Long-term treatment data of up to 2 years are now available, confirming efficacy and acceptable safety.
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