drugset / Trial / NCT00546793

Ph I/II Study of Subcutaneously Administered Veltuzumab (hA20) in NHL and CLL

NCT00546793

Phase 1/2 Completed 32 enrolled Gilead Sciences
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine if a subcutaneous (SC) dosing schedule of veltuzumab can be established in NHL or CLL patients and to confirm the safety and efficacy of veltuzumab that was previously established when administered intravenously.

Timeline

Start
2008-01
Primary completion
2013-03
Completion
2013-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject veltuzumab Monoclonal antibody 80 mg Subcutaneous
Subject veltuzumab Monoclonal antibody 160 mg Subcutaneous
Subject veltuzumab Monoclonal antibody 320 mg Subcutaneous