drugset / Trial / NCT01202760

A Rheumatoid Arthritis Study in Participants

NCT01202760

Phase 3 Completed 1004 enrolled Eli Lilly and Company
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary purpose of this study is to help answer if LY2127399 is safe and effective in the treatment of rheumatoid arthritis with or without background disease-modifying anti-rheumatic drug (DMARD) therapy. This study is comprised of 2 periods: Period 1 - 24-week blinded treatment Period 2 - 48-week post-treatment follow-up

Timeline

Start
2011-01
Primary completion
2012-12
Completion
2013-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Tabalumab Monoclonal antibody 90 mg Subcutaneous
Subject Tabalumab Monoclonal antibody 120 mg Subcutaneous

Indications