Balsalazide is more effective and better tolerated than mesalamine in the treatment of acute ulcerative colitis. The Abacus Investigator Group
- PMID: 9428213
- DOI: 10.1016/s0016-5085(98)70627-4
Balsalazide is more effective and better tolerated than mesalamine in the treatment of acute ulcerative colitis. The Abacus Investigator Group
Abstract
Background & aims: Aminosalicylates are widely used in the treatment of ulcerative colitis (UC). Balsalazide is a novel mesalamine prodrug, activated by colonic bacteria. The aim of this study was to compare the efficacy and safety of balsalazide with that of a pH-dependent formulation of mesalamine in active UC.
Methods: A randomized, double-blind study was performed comparing balasalazide, 6.75 g daily, with mesalamine, 2.4 g daily, administered for 4, 8, or 12 weeks to 101 (99 evaluable) patients with symptomatic, sigmoidoscopically verified UC.
Results: More patients treated with balsalazide achieved symptomatic remission after 2 (64% [balsalazide] vs. 43% [mesalamine]), 4 (70% vs. 51%), 8 (78% vs. 45%), and 12 weeks (88% vs. 57%) and complete remission (none/mild symptoms, sigmoidoscopy grade 0/1, no rectal steroid use within 4 days) after 4 (38% vs. 12%), 8 (54% vs. 22%), and 12 weeks (62% vs. 37%). Patients taking balsalazide experienced more asymptomatic days (4 weeks, 24% vs. 14%) and achieved the first asymptomatic day more rapidly (median, 10 vs. 25 days). Fewer patients in the balsalazide group reported adverse events (48% vs. 71%); four serious adverse events occurred in the mesalamine group.
Conclusions: Balsalazide is more effective and better tolerated than mesalamine as treatment for acute UC.
Comment in
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Efficacy of different mesalamine-releasing drugs.Gastroenterology. 1998 Nov;115(5):1306-7. doi: 10.1016/s0016-5085(98)70119-2. Gastroenterology. 1998. PMID: 9797396 No abstract available.
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Balsalazide and azathiprine or 6-mercaptopurine: evidence for a potentially serious drug interaction.Gastroenterology. 1999 Jun;116(6):1505-6. doi: 10.1016/s0016-5085(99)70524-x. Gastroenterology. 1999. PMID: 10391741 No abstract available.
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