Viewing Study NCT00094159



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Last Modification Date: 2024-10-26 @ 9:10 AM
Study NCT ID: NCT00094159
Status: COMPLETED
Last Update Posted: 2007-05-10
First Post: 2004-10-14

Brief Title: Safety Assessment of Weekly Intravenous Infusions of SNS-595 for the Treatment of Solid Tumors
Sponsor: Sunesis Pharmaceuticals
Organization: Sunesis Pharmaceuticals

Study Overview

Official Title: Phase I Open-Label Multicenter Dose-Escalation Clinical Study of the Safety and Pharmacokinetic Profiles of Weekly Intravenous Administrations of SNS-595 in Patients With Advanced Malignancies
Status: COMPLETED
Status Verified Date: 2007-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to determine whether SNS-595 given intravenously weekly for 3 weeks is safe
Detailed Description: Other objectives of this study include measuring pharmacokinetics how long the drug can be measured in the blood and determining the dose and dose schedule for the next phase of studies with SNS-595

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None