drugset / Trial / NCT01706926

A Study of Mavrilimumab in Subjects With Moderate-to-Severe Rheumatoid Arthritis

NCT01706926

Phase 2 Completed 420 enrolled MedImmune LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the efficacy of 3 subcutaneous doses of mavrilimumab compared with placebo in combination with methotrexate (MTX) in subjects with moderate-to-severe adult onset Rheumatoid Arthritis (RA).

Timeline

Start
2012-08
Primary completion
2013-12
Completion
2014-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Mavrilimumab Monoclonal antibody 30 mg Subcutaneous
Subject Mavrilimumab Monoclonal antibody 100 mg Subcutaneous
Subject Mavrilimumab Monoclonal antibody 150 mg Subcutaneous

Indications