drugset / Trial / NCT01662102

Rituximab or Zevalin - Efficacy Trial of Therapeutic Alternatives (RoZetta)

NCT01662102

Phase 3 Terminated 1 enrolled Spectrum Pharmaceuticals, Inc
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the effect of consolidation treatment Zevalin® versus maintenance treatment with Rituxan® on progression-free survival (PFS) following response induction with chemotherapy plus rituximab in previously untreated participants with follicular lymphoma.

Timeline

Start
2012-12-11
Primary completion
2013-03-05
Completion
2013-03-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Rituximab Monoclonal antibody 250 mg/m2 Intravenous
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous
Subject ibritumomab tiuxetan Monoclonal antibody 0.3 unknown Intravenous
Subject ibritumomab tiuxetan Monoclonal antibody 14.8 mbq/kg Intravenous

Indications