drugset / Trial / NCT01369329

A Study to Evaluate the Safety and Efficacy of Ustekinumab in Patients With Moderately to Severely Active Crohn's Disease Who Have Failed or Are Intolerant to Tumor Necrosis Factor (TNF) Antagonist Therapy (UNITI-1)

NCT01369329 ↗

Phase 3 Completed 769 enrolled Janssen Research & Development, LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study (UNITI-1) will compare the effects (both positive and negative) of an initial treatment with ustekinumab to placebo over 8 weeks, in patients with moderately to severely active Crohn's disease who have either failed or could not tolerate at least one TNF-antagonist medications in the past (specifically, infliximab, adalimumab, or certolizumab pegol).

Timeline

Start
2011-07
Primary completion
2013-06
Completion
2013-07

Outcome

Met primary endpoint

paper were significantly higher than the rates among patients receiving placebo (in UNITI-1, 34.3%, 33.7%, and 21.5%, respectively PMID 27959607 ↗

registry Placebo vs Ustekinumab 130 Milligram (mg); p = 0.002 NCT01369329 ↗

registry Placebo vs Ustekinumab Approximately (~) 6 Milligram Per Kilogram (mg/kg); p = 0.003 NCT01369329 ↗

release “UNITI-1 demonstrated signicantly higher rates of clinical response at Week 6” jnj.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ustekinumab Monoclonal antibody 6 mg/kg Intravenous
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