drugset / Trial / NCT00783692

Study of Vedolizumab (MLN0002) in Patients With Moderate to Severe Crohn's Disease

NCT00783692

Phase 3 Completed 1116 enrolled Millennium Pharmaceuticals, Inc.
RandomizedFactorialTriple-blindTreatment

Summary

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

Timeline

Start
2008-12
Primary completion
2012-03
Completion
2012-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vedolizumab Monoclonal antibody 300 mg Intravenous

Indications