drugset / Trial / NCT01202773

A Study in Participants With Rheumatoid Arthritis

NCT01202773

Phase 3 Terminated 456 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 in participants with an inadequate response to one or more tumor necrosis factor-alpha (TNF-α) inhibitors. 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
2013-03
Completion
2014-01

Drugs

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

Indications