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A Study of the Safety and Efficacy of Infliximab (Remicade) in Subjects with Fistulizing Crohn''s Disease - Article


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Clinical Trial: A Study of the Safety and Efficacy of Infliximab (Remicade) in Subjects with Fistulizing Crohn''s Disease

This study is not yet open for patient recruitment.
Verified by Centocor Research & Development, Inc., PA, USA September 2005

Sponsored by: Centocor Research & Development, Inc., PA, USA
Information provided by: Centocor Research & Development, Inc., PA, USA
ClinicalTrials.gov Identifier: NCT00207766

Purpose

A study of infliximab in patients with Fistulizing Crohn''''s Disease
Condition Intervention Phase
Crohn Disease
 Drug: Infliximab 5 or 10 mg/kg or placebo
Phase III

MedlinePlus related topics:  Crohn''''s Disease

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Official Title: ACCENT II - A Randomized, Double-Blind, Placebo-Controlled Trial of Anti-TNF Chimeric Monoclonal Antibody (Infliximab, Remicade) in the Long Term Treatment of Patients with Fistulizing CROHN''''S Disease

Further Study Details: 
Primary Outcomes: Reduction in the number of draining fistulas
Secondary Outcomes: Complete fistula response (no draining fistula).
Expected Total Enrollment:  300

This is a medical research study for patients with Crohn''''s disease who have one or more draining enterocutaneous fistula (fistula from the bowel to the skin). Fistulas are a common complication of Crohn''''s disease. Fistulas rarely close spontaneously but they may get better with treatment of the underlying Crohn''''s disease. This study will investigate the safety and efficacy of maintenance dosing of an anti-TNF (anti-tumor necrosis factor) antibody (a protein), called infliximab, compared to a placebo (inactive substance) in providing sustained reductions in the number of draining fistulas.

Subjects will receive infliximab at weeks 0, 2 and 6 followed by infusions of infliximab 5 mg/kg or placebo at weeks 14 and every 8 weeks until week 46. Patients who lose response are eligible for increasing treatment by 5 mg/kg of infliximab.

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria: - Single or multiple draining fistulas - Crohn''''s disease of at least 3 months'''' duration,

Exclusion Criteria: - Crohn''''s disease complications for which surgery might be indicated - positive stool culture

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00207766

For more information please see the link below or email       info@veritasmedicine.com

Study chairs or principal investigators

Centocor Research & Development, Inc., PA, USA Clinical Trial,  Study Director,  Centocor Research & Development, Inc., PA, USA   

More Information

Study ID Numbers:  CR005413
Last Updated:  September 20, 2005
Record first received:  September 13, 2005
ClinicalTrials.gov Identifier:  NCT00207766
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-09-27


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