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Cited by 3,902

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Infliximab for Induction and Maintenance Therapy for Ulcerative Colitis

Open access
Rutgeerts, Paul, Sandborn, William J., Feagan, Brian G., Reinisch, Walter, Olson, Allan, Johanns, Jewel, Travers, Suzanne, Rachmilewitz, Daniel, Hanauer, Stephen B., Lichtenstein, Gary R., de Villiers, Willem J.S., Present, Daniel, Sands, Bruce E., Colombel, Jean Frédéric·2005·New England Journal of Medicine

Abstract

BACKGROUND: Infliximab, a chimeric monoclonal antibody directed against tumor necrosis factor alpha, is an established treatment for Crohn's disease but not ulcerative colitis. METHODS: Two randomized, double-blind, placebo-controlled studies--the Active Ulcerative Colitis Trials 1 and 2 (ACT 1 and ACT 2, respectively)--evaluated the efficacy of infliximab for induction and maintenance therapy in adults with ulcerative colitis. In each study, 364 patients with moderate-to-severe active ulcerative colitis despite treatment with concurrent medications received placebo or infliximab (5 mg or 10 mg per kilogram of body weight) intravenously at weeks 0, 2, and 6 and then every eight weeks through week 46 (in ACT 1) or week 22 (in ACT 2). Patients were followed for 54 weeks in ACT 1 and 30 weeks in ACT 2. RESULTS: In ACT 1, 69 percent of patients who received 5 mg of infliximab and 61 percent of those who received 10 mg had a clinical response at week 8, as compared with 37 percent of those who received placebo (P<0.001 for both comparisons with placebo). A response was defined as a decrease in the Mayo score of at least 3 points and at least 30 percent, with an accompanying decrease in the subscore for rectal bleeding of at least 1 point or an absolute rectal-bleeding subscore of 0 or 1. In ACT 2, 64 percent of patients who received 5 mg of infliximab and 69 percent of those who received 10 mg had a clinical response at week 8, as compared with 29 percent of those who received placebo (P<0.001 for both comparisons with placebo). In both studies, patients who received infliximab were more likely to have a clinical response at week 30 (P< or =0.002 for all comparisons). In ACT 1, more patients who received 5 mg or 10 mg of infliximab had a clinical response at week 54 (45 percent and 44 percent, respectively) than did those who received placebo (20 percent, P<0.001 for both comparisons). CONCLUSIONS: Patients with moderate-to-severe active ulcerative colitis treated with infliximab at weeks 0, 2, and 6 and every eight weeks thereafter were more likely to have a clinical response at weeks 8, 30, and 54 than were those receiving placebo. (ClinicalTrials.gov numbers, NCT00036439 and NCT00096655.)

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Metadata

Authors
Rutgeerts, P., Sandborn, W. J., Feagan, B. G., Reinisch, W., Olson, A., Johanns, J., Travers, S., Rachmilewitz, D., Hanauer, S. B., Lichtenstein, G. R., de Villiers, W. J. S., Present, D., Sands, B. E., & Colombel, J. F.
Venue
New England Journal of Medicine
Published
2005-12-08
Volume
353
Issue
23
Pages
2462-2476
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2171297959
Cited by
3,902
References
1
FWCI
77.98
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Infliximab for Induction and Maintenance Therapy for Ulcerative Colitis. https://app.cochat.ai/papers/10.1056/nejmoa050516
The paper
Rutgeerts, P., Sandborn, W. J., Feagan, B. G., Reinisch, W., Olson, A., Johanns, J., Travers, S., Rachmilewitz, D., Hanauer, S. B., Lichtenstein, G. R., de Villiers, W. J. S., Present, D., Sands, B. E., & Colombel, J. F. (2005). Infliximab for Induction and Maintenance Therapy for Ulcerative Colitis. New England Journal of Medicine. https://doi.org/10.1056/nejmoa050516

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