drugset / Trial / NCT00408603

Safety and Efficacy Clinical Study of SNS-595 in Patients With Platinum-Resistant Ovarian Cancer

NCT00408603

Phase 2 Completed 183 enrolled Sunesis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the objective response rate, safety and identify potential biomarkers in platinum-resistant ovarian cancer patients treated with voreloxin injection given on a 28-day cycle.

Timeline

Start
2006-12-20
Primary completion
2010-06-09
Completion
2010-06-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Vosaroxin Small molecule 48 mg/m2
Subject Vosaroxin Small molecule 60 mg/m2
Subject Vosaroxin Small molecule 75 mg/m2