drugset / Trial / NCT02296775

Comparative Pharmacokinetic, Pharmacodynamic, Safety and Efficacy Study of Three Anti-CD20 Monoclonal Antibodies in Patients With Moderate to Severe Rheumatoid Arthritis

NCT02296775 ↗

Phase 1/2 Completed 276 enrolled Dr. Reddy's Laboratories Limited
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will compare the plasma pharmacokinetic profile and the change in disease activity score in patients with active rheumatoid arthritis following treatment with two 1000 mg doses of DRL\_RI or one of two sources of rituximab (Rituxan® or MabThera®). Patients will also be monitored for safety, B cell depletion and recovery, and for the development of immune responses to the administered study drugs

Timeline

Start
2014-11
Primary completion
2016-11
Completion
2017-10-05

Drugs

EvaluationDrugModalityDoseRoute
Subject DRL_RI Unknown 1000 mg Intravenous
Comparator Rituximab Monoclonal antibody 1000 mg Intravenous

Indications