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

Outcome

Met primary endpoint

registry Placebo vs Ustekinumab 130 mg; p < 0.001; Cochran-Mantel-Haenszel chi-square test NCT01369342 ↗

paper those receiving intravenous ustekinumab had a significantly higher rate of response than did those receiving placebo. PMID 27959607 ↗

release “The Phase 3 Janssen Research & Development, LLC-sponsored UNITI-2 study achieved its primary endpoint” jnj.com ↗

release “UNITI-2 also demonstrated signicantly greater clinical response at Week 6 with IV ustekinumab induction compared to IV placebo” jnj.com ↗

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