drugset / Trial / NCT00528073

Placebo Controlled Study of 3 Doses of Rifaximin-EIR Tablet to Treat Moderate, Active Crohn's Disease

NCT00528073

Phase 2 Completed 410 enrolled Alfasigma S.p.A.
RandomizedParallel-groupTriple-blindTreatment

Summary

This study aims to determine which of 3 doses of a non-absorbable antibiotic Rifaximin is most effective in treating active moderate Crohn's disease. Rifaximin tablets are already marketed in some European countries and the USA to treat traveller's diarrhoea. A new gastro-resistant form of Rifaximin called Rifaximin-Extended Intestinal Release (EIR) will be used in this study. These tablets dissolve in the stomach,releasing gastro-resistant granules which pass into the intestines and deliver Rifaximin directly to the site of the disease. Rifaximin is not absorbed, making it more effective and greatly reducing the frequency of side effects.

Timeline

Start
2007-09
Primary completion
2009-03
Completion
2009-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Rifaximin Other / unclassified 400 mg Oral
Subject Rifaximin Other / unclassified 800 mg Oral
Subject Rifaximin Other / unclassified 1200 mg Oral

Indications