drugset / Trial / NCT00048555

Safety and Efficacy of IDEC-114 in Combination With Rituxan in the Treatment of Non-Hodgkin's Lymphoma

NCT00048555 ↗

Phase 1/2 Completed 90 enrolled Biogen
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To determine what side effects and what clinical effect, if any, the administration of this investigational product, IDEC-114 in combination with Rituxan® \[Rituxan® as a single agent is approved by the United States Food and Drug Administration (FDA) to treat patients with relapsed or refractory follicular NHL\], has in this patient population.

Timeline

Start
2002-11
Primary completion
2004-03
Completion
2010-11

Drugs

EvaluationDrugModalityDoseRoute
Subject galiximab Monoclonal antibody 125 mg/m2 —
Subject galiximab Monoclonal antibody 250 mg/m2 —
Subject galiximab Monoclonal antibody 375 mg/m2 —
Subject galiximab Monoclonal antibody 500 mg/m2 —
Background Rituximab Monoclonal antibody 375 mg/m2 —

Indications