drugset / Trial / NCT00783718

Study of Vedolizumab (MLN0002) in Patients With Moderate to Severe Ulcerative Colitis

NCT00783718

Phase 3 Completed 895 enrolled Millennium Pharmaceuticals, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary purpose of this study was to determine the effect of vedolizumab induction treatment on clinical response at 6 weeks and to determine the effect of vedolizumab maintenance treatment on clinical remission at 52 weeks.

Timeline

Start
2009-01
Primary completion
2011-12
Completion
2012-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vedolizumab Monoclonal antibody 300 mg Intravenous

Indications