drugset / Trial / NCT02693210

A Study to Evaluate the Efficacy and Safety of Mabthera Alone and in Combination With Either Cyclophosphamide or Methotrexate in Patients With Rheumatoid Arthritis

NCT02693210 ↗

Phase 2 Completed 161 enrolled Hoffmann-La Roche
RandomizedParallel-groupTriple-blindTreatment

Summary

WA16291 is a Phase IIa "proof-of-concept" study. The primary objective of this study is to determine the safety and efficacy of rituximab (a B cell depleting chimeric monoclonal antibody) used either as monotherapy or in combination with methotrexate or cyclophosphamide in participants with rheumatoid arthritis who have failed prior Disease Modifying Anti-Rheumatic Drug (DMARD) therapy and currently have an inadequate clinical response to methotrexate.

Timeline

Start
2001-02
Primary completion
2002-08
Completion
2004-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 750 mg —
Subject Methotrexate Small molecule 10 mg Oral
Subject Rituximab Monoclonal antibody 1 g Intravenous

Indications