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Patient considerations in the management of ulcerative colitis – role of vedolizumab

Ulcerative colitis (UC) is a subtype of inflammatory bowel disease which causes inflammation of the large intestine and affects approximately 7.6–24.6 per 100,000 persons. The therapeutic goal for UC patients is inducing remission, maintaining remission, and ideally, obtaining mucosal healing. Vedol...

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Detalles Bibliográficos
Autores principales: Kothari, Megha, Mudireddy, Prashant, Swaminath, Arun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4548764/
https://www.ncbi.nlm.nih.gov/pubmed/26316768
http://dx.doi.org/10.2147/TCRM.S65650
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author Kothari, Megha
Mudireddy, Prashant
Swaminath, Arun
author_facet Kothari, Megha
Mudireddy, Prashant
Swaminath, Arun
author_sort Kothari, Megha
collection PubMed
description Ulcerative colitis (UC) is a subtype of inflammatory bowel disease which causes inflammation of the large intestine and affects approximately 7.6–24.6 per 100,000 persons. The therapeutic goal for UC patients is inducing remission, maintaining remission, and ideally, obtaining mucosal healing. Vedolizumab, approved by the US Food and Drug Administration in May 2014 for the treatment of moderate-to-severe UC and Crohn’s disease, is a newly developed anti-integrin therapy. This review focuses on the preclinical development of vedolizumab and data from early trials, and details the results of the landmark trails that led to its approval in the USA with a specific focus on the management of UC. Additionally, data on safety and the current UC management protocols are also discussed.
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spelling pubmed-45487642015-08-27 Patient considerations in the management of ulcerative colitis – role of vedolizumab Kothari, Megha Mudireddy, Prashant Swaminath, Arun Ther Clin Risk Manag Review Ulcerative colitis (UC) is a subtype of inflammatory bowel disease which causes inflammation of the large intestine and affects approximately 7.6–24.6 per 100,000 persons. The therapeutic goal for UC patients is inducing remission, maintaining remission, and ideally, obtaining mucosal healing. Vedolizumab, approved by the US Food and Drug Administration in May 2014 for the treatment of moderate-to-severe UC and Crohn’s disease, is a newly developed anti-integrin therapy. This review focuses on the preclinical development of vedolizumab and data from early trials, and details the results of the landmark trails that led to its approval in the USA with a specific focus on the management of UC. Additionally, data on safety and the current UC management protocols are also discussed. Dove Medical Press 2015-08-19 /pmc/articles/PMC4548764/ /pubmed/26316768 http://dx.doi.org/10.2147/TCRM.S65650 Text en © 2015 Kothari et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Kothari, Megha
Mudireddy, Prashant
Swaminath, Arun
Patient considerations in the management of ulcerative colitis – role of vedolizumab
title Patient considerations in the management of ulcerative colitis – role of vedolizumab
title_full Patient considerations in the management of ulcerative colitis – role of vedolizumab
title_fullStr Patient considerations in the management of ulcerative colitis – role of vedolizumab
title_full_unstemmed Patient considerations in the management of ulcerative colitis – role of vedolizumab
title_short Patient considerations in the management of ulcerative colitis – role of vedolizumab
title_sort patient considerations in the management of ulcerative colitis – role of vedolizumab
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4548764/
https://www.ncbi.nlm.nih.gov/pubmed/26316768
http://dx.doi.org/10.2147/TCRM.S65650
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