drugset / Trial / NCT00446342

Study of Intravenously Administered SNS-032 in Patients With Advanced B-lymphoid Malignancies

NCT00446342 ↗

Phase 1 Completed 21 enrolled Sunesis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety and tolerability of escalating doses of SNS-032, given in 3 weekly administrations per cycle and to identify a recommended Phase 2 dose.

Timeline

Start
2007-02
Primary completion
2008-12
Completion
2009-03

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-387032 Small molecule 15 mg/m2 Intravenous
Subject BMS-387032 Small molecule 70 mg/m2 Intravenous