drugset / Trial / NCT01369355

A Study to Evaluate the Safety and Efficacy of Ustekinumab Maintenance Therapy in Patients With Moderately to Severely Active Crohn's Disease (IM-UNITI)

NCT01369355

Phase 3 Completed 1282 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of this study is to evaluate the efficacy and safety of 2 maintenance regimens of ustekinumab administered subcutaneously to patients with moderately to severely active Crohn's disease who responded to treatment with intravenous ustekinumab in studies CNTO1275CRD3001 and CNTO1275CRD3002, compared to subcutaneously administered placebo.

Timeline

Start
2011-09-13
Primary completion
2015-06-10
Completion
2019-10-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ustekinumab Monoclonal antibody 90 mg Subcutaneous
Subject Ustekinumab Monoclonal antibody 130 mg Subcutaneous

Indications