Delayed-Release Oral Mesalamine 4.8 g/day (800 mg tablets) Compared with 2.4 g/day (400 mg tablets) for the Treatment of Mildly to Moderately Active Ulcerative Colitis: The ASCEND I Trial
BACKGROUND: Delayed-release oral mesalamine 2.4 g/day to 4.8 g/day has been shown to be effective in treating mildly to moderately active ulcerative colitis (UC), but it is unknown whether an initial dose of 4.8 g/day is more effective than 2.4 g/day in patients with mildly to moderately active UC a...
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Series: | Canadian Journal of Gastroenterology |
Online Access: | http://dx.doi.org/10.1155/2007/862917 |
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doaj-ad3278ef9a5649a2863d0e867761ade82020-11-25T00:37:00ZengHindawi LimitedCanadian Journal of Gastroenterology0835-79002007-01-01211282783410.1155/2007/862917Delayed-Release Oral Mesalamine 4.8 g/day (800 mg tablets) Compared with 2.4 g/day (400 mg tablets) for the Treatment of Mildly to Moderately Active Ulcerative Colitis: The ASCEND I TrialStephen B Hanauer0William J Sandborn1Christian Dallaire2André Archambault3Bruce Yacyshyn4Chyon Yeh5Nancy Smith-Hall6University of Chicago School of Medicine, Chicago, Illinois, USADivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota, USAUniversité Laval, Québec, CanadaUniversité de Montréal, Montréal, Québec, CanadaProcter & Gamble Pharmaceuticals, Mason, Ohio, USAProcter & Gamble Pharmaceuticals, Mason, Ohio, USAProcter & Gamble Pharmaceuticals, Mason, Ohio, USABACKGROUND: Delayed-release oral mesalamine 2.4 g/day to 4.8 g/day has been shown to be effective in treating mildly to moderately active ulcerative colitis (UC), but it is unknown whether an initial dose of 4.8 g/day is more effective than 2.4 g/day in patients with mildly to moderately active UC and in the subgroup with moderate disease.http://dx.doi.org/10.1155/2007/862917 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Stephen B Hanauer William J Sandborn Christian Dallaire André Archambault Bruce Yacyshyn Chyon Yeh Nancy Smith-Hall |
spellingShingle |
Stephen B Hanauer William J Sandborn Christian Dallaire André Archambault Bruce Yacyshyn Chyon Yeh Nancy Smith-Hall Delayed-Release Oral Mesalamine 4.8 g/day (800 mg tablets) Compared with 2.4 g/day (400 mg tablets) for the Treatment of Mildly to Moderately Active Ulcerative Colitis: The ASCEND I Trial Canadian Journal of Gastroenterology |
author_facet |
Stephen B Hanauer William J Sandborn Christian Dallaire André Archambault Bruce Yacyshyn Chyon Yeh Nancy Smith-Hall |
author_sort |
Stephen B Hanauer |
title |
Delayed-Release Oral Mesalamine 4.8 g/day (800 mg tablets) Compared with 2.4 g/day (400 mg tablets) for the Treatment of Mildly to Moderately Active Ulcerative Colitis: The ASCEND I Trial |
title_short |
Delayed-Release Oral Mesalamine 4.8 g/day (800 mg tablets) Compared with 2.4 g/day (400 mg tablets) for the Treatment of Mildly to Moderately Active Ulcerative Colitis: The ASCEND I Trial |
title_full |
Delayed-Release Oral Mesalamine 4.8 g/day (800 mg tablets) Compared with 2.4 g/day (400 mg tablets) for the Treatment of Mildly to Moderately Active Ulcerative Colitis: The ASCEND I Trial |
title_fullStr |
Delayed-Release Oral Mesalamine 4.8 g/day (800 mg tablets) Compared with 2.4 g/day (400 mg tablets) for the Treatment of Mildly to Moderately Active Ulcerative Colitis: The ASCEND I Trial |
title_full_unstemmed |
Delayed-Release Oral Mesalamine 4.8 g/day (800 mg tablets) Compared with 2.4 g/day (400 mg tablets) for the Treatment of Mildly to Moderately Active Ulcerative Colitis: The ASCEND I Trial |
title_sort |
delayed-release oral mesalamine 4.8 g/day (800 mg tablets) compared with 2.4 g/day (400 mg tablets) for the treatment of mildly to moderately active ulcerative colitis: the ascend i trial |
publisher |
Hindawi Limited |
series |
Canadian Journal of Gastroenterology |
issn |
0835-7900 |
publishDate |
2007-01-01 |
description |
BACKGROUND: Delayed-release oral mesalamine 2.4 g/day to 4.8 g/day has been shown to be effective in treating mildly to moderately active ulcerative colitis (UC), but it is unknown whether an initial dose of 4.8 g/day is more effective than 2.4 g/day in patients with mildly to moderately active UC and in the subgroup with moderate disease. |
url |
http://dx.doi.org/10.1155/2007/862917 |
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