drugset / Trial / NCT00161564

A Trial to Treat Patients With ITP Who Do Not Achieve a Durable Response to Rituxan Alone

NCT00161564 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this research study is to compare the efficacy and safety of higher doses of rituximab to a combination of standard doses of Rituxan + CVP (Cyclophosphamide, Vincristine, and Prednisone) in patients with chronic Idiopathic Thrombocytopenic Purpura (ITP who did not respond to or relapsed after standard doses of rituximab.

Timeline

Start
2004-02
Primary completion
—
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Rituximab Monoclonal antibody 750 mg/m2 —