drugset / Trial / NCT01463059

Efficacy and Safety of Olokizumab With Rheumatoid Arthritis With Previously Failed to Anti-tumor Necrosis Factor (Anti-TNF) Therapy

NCT01463059

Phase 2 Completed 119 enrolled UCB Japan Co. Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to evaluate the efficacy and safety of CDP6038 administered subcutaneous (sc) at various doses compared to placebo.

Timeline

Start
2011-10
Primary completion
2013-02
Completion
2013-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Olokizumab Monoclonal antibody 60 mg Subcutaneous
Subject Olokizumab Monoclonal antibody 120 mg Subcutaneous
Subject Olokizumab Monoclonal antibody 240 mg Subcutaneous

Indications