drugset / Trial / NCT01369342

A Study to Evaluate the Safety and Efficacy of Ustekinumab Induction Therapy in Patients With Moderately to Severely Active Crohn's Disease (UNITI-2)

NCT01369342

Phase 3 Completed 640 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study (UNITI-2) will compare the effects (both positive and negative) of an initial treatment with ustekinumab to a placebo over 8 weeks in patients with moderately to severely active Crohn's disease.

Timeline

Start
2011-07
Primary completion
2014-08
Completion
2014-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ustekinumab Monoclonal antibody 130 mg Intravenous
Subject Ustekinumab Monoclonal antibody 260 mg Intravenous
Subject Ustekinumab Monoclonal antibody 390 mg Intravenous
Subject Ustekinumab Monoclonal antibody 520 mg Intravenous

Indications