drugset / Trial / NCT01290549

A Study of Escalating Doses of Polatuzumab Vedotin in Participants With Relapsed or Refractory B-Cell Non-Hodgkins Lymphoma and Chronic Lymphocytic Leukemia and Polatuzumab Vedotin in Combination With Rituximab in Participants With Relapsed or Refractory B-Cell Non-Hodgkins Lymphoma

NCT01290549

Phase 1 Completed 95 enrolled Genentech, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is a Phase I, multicenter, open-label, dose-escalation study of polatuzumab vedotin administered as a single agent by intravenous (IV) infusion to participants with relapsed or refractory hematologic malignancies. In Phase Ib, participants will receive polatuzumab vedotin in combination with rituximab.

Timeline

Start
2011-03-22
Primary completion
2012-06-29
Completion
2014-11-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Polatuzumab Vedotin Other / unclassified 0.1 mg/kg Intravenous
Subject Polatuzumab Vedotin Other / unclassified 0.25 mg/kg Intravenous
Subject Polatuzumab Vedotin Other / unclassified 0.5 mg/kg Intravenous
Subject Polatuzumab Vedotin Other / unclassified 1 mg/kg Intravenous
Subject Polatuzumab Vedotin Other / unclassified 1.8 mg/kg Intravenous
Subject Polatuzumab Vedotin Other / unclassified 2 mg/kg Intravenous
Subject Polatuzumab Vedotin Other / unclassified 2.4 mg/kg Intravenous
Subject Polatuzumab Vedotin Other / unclassified 4 mg/kg Intravenous
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous