drugset / Trial / NCT00720538

Summary

Several open-label studies reported thalidomide efficacy in inducing clinical remission and steroid tapering in refractory Inflammatory Bowel diseases (IBD), both in adults and in children. This is a randomized placebo controlled (RCT) double blind study, to evaluate the efficacy of thalidomide in inducing clinical remission at 8 weeks in refractory IBD patients aged 2-20 years. The primary hypotheses of the study is that thalidomide would be more effective than placebo in inducing clinical remission. The RCT phase is followed by a open-label phase, to further evaluate efficacy and safety of thalidomide in thalidomide responders, with a total follow up of one year.

Timeline

Start
2008-08
Primary completion
2011-09
Completion
2012-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Thalidomide Other / unclassified 1.5 mg/kg
Subject Thalidomide Other / unclassified 2.5 mg/kg