drugset / Trial / NCT01768572

To Evaluate The Safety of SAR153191 (REGN88) and Tocilizumab Added to Other RA Drugs in Patients With RA Who Are Not Responding to or Intolerant of Anti-TNF Therapy (SARIL-RA-ASCERTAIN)

NCT01768572

Phase 3 Completed 202 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Primary Objective: To assess, in the same study, the safety of sarilumab and tocilizumab in participants with rheumatoid arthritis (RA) who were inadequate responders to or intolerant of tumor necrosis factor (TNF) antagonists.

Timeline

Start
2013-03
Primary completion
2014-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Sarilumab Monoclonal antibody 150 mg Subcutaneous
Subject Sarilumab Monoclonal antibody 200 mg Subcutaneous
Comparator Tocilizumab Monoclonal antibody 4 mg/kg Intravenous
Comparator Tocilizumab Monoclonal antibody 8 mg/kg Intravenous
Background Hydroxychloroquine Small molecule
Background Leflunomide Small molecule
Background Methotrexate Small molecule
Background Sulfasalazine Small molecule

Indications