drugset / Trial / NCT01050998

A Study to Evaluate the Efficacy and Safety of CAM-3001 (Drug) in Subjects With Rheumatoid Arthritis

NCT01050998

Phase 2 Completed 516 enrolled MedImmune LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objectives of this study is to assess the safety, tolerability and efficacy of multiple doses of the mavrilimumab (CAM-3001) administered subcutaneously in subjects with moderately active Rheumatoid Arthritis (RA).

Timeline

Start
2010-01-05
Primary completion
2011-06-09
Completion
2012-07-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Mavrilimumab Monoclonal antibody 10 mg Subcutaneous
Subject Mavrilimumab Monoclonal antibody 30 mg Subcutaneous
Subject Mavrilimumab Monoclonal antibody 50 mg Subcutaneous
Subject Mavrilimumab Monoclonal antibody 100 mg Subcutaneous

Indications