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

Outcome

Mixed primary results

registry Placebo vs DB Vedolizumab; p = 0.0206; Risk Difference (RD) 7.8 (95% CI 1.2 to 14.3) NCT00783692 ↗

registry Placebo vs DB Vedolizumab; p = 0.2322; Risk Difference (RD) 5.7 (95% CI -3.6 to 15.0) NCT00783692 ↗

registry Placebo vs Vedolizumab Q8W; p = 0.0007; Risk Difference (RD) 17.4 (95% CI 7.3 to 27.5) NCT00783692 ↗

registry Placebo vs Vedolizumab Q4W; p = 0.0042; Risk Difference (RD) 14.7 (95% CI 4.6 to 24.7) NCT00783692 ↗

paper Vedolizumab-treated patients with active Crohn's disease were more likely than patients receiving placebo to have a remission, but not a CDAI-100 response, at week 6 PMID 23964933 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vedolizumab Monoclonal antibody 300 mg Intravenous

Indications