drugset / Trial / NCT01059448

Safety and Efficacy of AMG 827 in Subjects With RA

NCT01059448

Phase 2 Terminated 211 enrolled Amgen
NaSingle-groupOpen-labelTreatment

Summary

This is an extension study for subjects who participated in Protocol 20090061 (NCT00950989). All subjects in this study will receive a 210mg injection of AMG827 for treatment for their Rheumatoid Arthritis for up to 5 years.

Timeline

Start
2010-06-03
Primary completion
2011-04-05
Completion
2011-04-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Brodalumab Monoclonal antibody 210 mg Subcutaneous

Indications