drugset / Trial / NCT01253226

A Study for Japanese Participants With Rheumatoid Arthritis (RA)

NCT01253226

Phase 1 Completed 32 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will evaluate the safety and tolerability of multiple doses of LY2127399 (tabalumab) in Japanese participants with RA. The study consists of a 20-week treatment period. All participants will be followed for up to 12 weeks after the last study drug administration.

Timeline

Start
2009-09
Primary completion
2011-08
Completion
2011-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Tabalumab Monoclonal antibody 30 mg Subcutaneous
Subject Tabalumab Monoclonal antibody 60 mg Subcutaneous
Subject Tabalumab Monoclonal antibody 120 mg Subcutaneous

Indications