Study identifier:CD-IA-CAM-3001-1109
ClinicalTrials.gov identifier:NCT01712399
EudraCT identifier:N/A
CTIS identifier:N/A
An Open-label Extension Study to Evaluate the Long-term Safety of Mavrilimumab in Adult Subjects with Rheumatoid Arthritis
Rheumatoid Arthritis
Phase 2
No
-
All
409
Interventional
19 Years - 79 Years
Allocation: N/A
Endpoint Classification: Safety
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Apr 2017 by MedImmune, LLC
MedImmune, LLC
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Mavrilimumab 100 mg Participants will receive 100 mg mavrilimumab once in every 2 weeks (Q2W) subcutaneously for up to 3 years. | Biological/Vaccine: Mavrilimumab 100 mg Participants will receive 100 mg mavrilimumab once in every 2 weeks (Q2W) subcutaneously for up to 3 years |