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The Role of the Food and Drug Administration in Medical Therapy for Ulcerative Colitis

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Medical Therapy of Ulcerative Colitis

Abstract

Ulcerative colitis (UC) affects approximately 1 in 400 people internationally, with a higher prevalence in the Western hemisphere, although more recently incidence and prevalence rates have been rising in the rest of the world, particularly in Asia. The majority of UC patients are prescribed with medication for induction or maintenance of remission. In addition to standard therapies, recent developments in immunology have identified novel therapeutic pathways and biologic agents to treat inflammatory bowel disease. There are currently 11 drugs and biologic agents (including prednisolone, sulfasalazine, balsalazide, budesonide MMX, infliximab, adalimumab, golimumab, and different preparations of mesalamines) approved by the Food and Drug Administration (FDA) to treat UC. At present, there are 145 registered clinical trials evaluating therapeutics for managing adult UC, including drugs, biologic agents, and clinical tools for therapeutic monitoring of treatment response and disease activity.

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Correspondence to Conor Lahiff M.D. .

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Lahiff, C., Moss, A.C., Cheifetz, A.S. (2014). The Role of the Food and Drug Administration in Medical Therapy for Ulcerative Colitis. In: Lichtenstein, G. (eds) Medical Therapy of Ulcerative Colitis. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-1677-1_2

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  • DOI: https://doi.org/10.1007/978-1-4939-1677-1_2

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