drugset / Trial / NCT01635621

A Phase II Study to Assess the Efficacy and Safety of Olokizumab in Patients With Crohn's Disease

NCT01635621

Phase 2 Withdrawn UCB BIOSCIENCES, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this multi-centre, double blind-study is to evaluate the clinical response of patients with moderate to severe Cohn's Disease (CD) following treatment with different doses and dose regimens of Olokizumab, relative to placebo.

Timeline

Start
2012-06
Primary completion
2013-08
Completion
2013-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Olokizumab Monoclonal antibody 120 mg Subcutaneous
Subject Olokizumab Monoclonal antibody 240 mg Subcutaneous

Indications