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

Outcome

Met primary endpoint

registry Placebo vs DB Vedolizumab; p < 0.0001; Risk Difference (RD) 21.7 (95% CI 11.6 to 31.7) NCT00783718 ↗

registry Placebo vs Vedolizumab Q8W; p < 0.0001; Risk Difference (RD) 26.1 (95% CI 14.9 to 37.2) NCT00783718 ↗

registry Placebo vs Vedolizumab Q4W; p < 0.0001; Risk Difference (RD) 29.1 (95% CI 17.9 to 40.4) NCT00783718 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vedolizumab Monoclonal antibody 300 mg Intravenous

Indications