drugset / Trial / NCT00129337

Study of Bavituximab in Patients With Advanced Solid Tumor Malignancies

NCT00129337

Phase 1 Completed 28 enrolled Peregrine Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety of bavituximab when administered via a vein, and to examine how bavituximab behaves in the body - how quickly it is taken up by the body and how long it stays there. The effect of bavituximab on tumor responses will also be examined.

Timeline

Start
2005-06
Primary completion
2009-08
Completion
2009-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Bavituximab Monoclonal antibody 0.1 mg/kg Intravenous
Subject Bavituximab Monoclonal antibody 0.3 mg/kg Intravenous
Subject Bavituximab Monoclonal antibody 1 mg/kg Intravenous
Subject Bavituximab Monoclonal antibody 3 mg/kg Intravenous

Indications