drugset / Trial / NCT01373151

Phase IIB Rheumatoid Arthritis Dose Ranging Study for BMS-945429 in Subjects Who Are Not Responding to Methotrexate

NCT01373151

Phase 2 Completed 418 enrolled CSL Behring
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the effective dose of BMS-945429 in subjects with inadequate response to Methotrexate in the treatment of moderate to severe Rheumatoid Arthritis.

Timeline

Start
2011-06
Primary completion
2012-09
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Adalimumab Monoclonal antibody 40 mg Subcutaneous
Subject Clazakizumab Monoclonal antibody 25 mg Subcutaneous
Subject Clazakizumab Monoclonal antibody 100 mg Subcutaneous
Subject Clazakizumab Monoclonal antibody 200 mg Subcutaneous
Subject Methotrexate Small molecule 15 mg Oral

Indications