drugset / Trial / NCT00144508

Phase III Comparative Study(Open-Label) of MRA for Rheumatoid Arthritis(RA)

NCT00144508 ↗

Phase 3 Completed 306 enrolled Chugai Pharmaceutical
RandomizedParallel-groupOpen-labelTreatment

Summary

To evaluate clinical efficacy and tolerability of MRA, patients with RA are randomized to receive either MRA or conventional DMARDs.

Timeline

Start
2003-03
Primary completion
2004-05
Completion
2006-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Tocilizumab Monoclonal antibody 8 mg/kg —

Indications