Viewing Study NCT00102752



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Study NCT ID: NCT00102752
Status: COMPLETED
Last Update Posted: 2009-04-30
First Post: 2005-02-01

Brief Title: Study of Safety and Efficacy of Glufosfamide in Combination With Gemcitabine in Cancer
Sponsor: Threshold Pharmaceuticals
Organization: Threshold Pharmaceuticals

Study Overview

Official Title: A Phase 12 Dose-Escalation Study of the Safety Efficacy and Pharmacokinetics of Glufosfamide in Combination With Gemcitabine in Advanced Solid Tumors and Pancreatic Adenocarcinoma
Status: COMPLETED
Status Verified Date: 2009-04
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 the safety of glufosfamide when administered in combination with gemcitabine
Detailed Description: This study TH-CR-301 is a Phase 12 study that will evaluate the efficacy and safety of glufosfamide in combination with gemcitabine in advanced solid tumors or in first line treatment of pancreatic cancer

Study Hypothesis Glufosfamide in combination with gemcitabine may provide benefits in survival to patients with advanced solid tumors or metastatic pancreatic cancer

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