drugset / Trial / NCT01526057

A Pharmacokinetic/Pharmacodynamic Study Comparing PF-05280586 To Rituximab In Subjects With Active Rheumatoid Arthritis With An Inadequate Response To TNF Inhibitors (REFLECTIONS B328-01)

NCT01526057 ↗

Phase 2 Completed 220 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

In this study, patients with moderate to severe rheumatoid arthritis who are being treated with methotrexate will receive 2 intravenous treatments with either PF-05280586 or Rituxan (Rituximab) or MabThera (Rituximab). During the course of the study, the effects of the drugs will be assessed by sampling the levels of drug in the blood, blood cell counts, and by comparing these levels among the different treatments. Safety, tolerability and immunologic response also will be evaluated throughout.

Timeline

Start
2012-03-20
Primary completion
2013-08-13
Completion
2014-05-07

Drugs

EvaluationDrugModalityDoseRoute
Subject PF-05280586 Unknown 1000 mg Intravenous
Comparator Rituximab Monoclonal antibody 1000 mg Intravenous

Indications