CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 31 enrolled
Drug / intervention
SNS-595 Injectiondrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00252382
NCT00252382Phase 2Completed

Phase 2 Open-Label, Multicenter Clinical Study of the Safety and Efficacy of the Intravenous Administration of SNS-595 as Second-Line Chemotherapy in Patients With Advanced Non-Small Cell Lung Cancer (NSCLC)

Sunesis Pharmaceuticals·interventional·Posted Nov 11, 2005·Updated Sep 24, 2018

In Brief

A Phase 2 clinical trial evaluating SNS-595 Injection for Carcinoma, Non-Small-Cell Lung. Completed, enrolled 31 participants across 4 sites.

Detailed Summary

The purpose of this study is to evaluate the objective tumor response rate (based on the RECIST criteria) to SNS-595 as a second-line therapy in patients with advanced NSCLC.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedNov 11, 2005
Enrollment StartDec 27, 2005
Primary CompletionMar 5, 2007
Study CompletionNov 29, 2007
TodayJul 2, 2026
Enrollment to primary: 1.2 yearsPosted 20.6 years ago

Interventions

SNS-595 Injectiondrug

Vosaroxin (formerly voreloxin or SNS-595) is a first in class anticancer quinolone derivative, non anthracycline topoisomerase II inhibitor. It induces replication dependent DNA damage by intercalating DNA and inhibiting topoisomerase II, leading to apoptosis.