Viewing Study NCT00160030



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Last Modification Date: 2024-10-26 @ 9:15 AM
Study NCT ID: NCT00160030
Status: COMPLETED
Last Update Posted: 2009-12-07
First Post: 2005-09-09

Brief Title: Study Comparing Radiochemotherapy With Folfox 4 Regimen or 5FU-Cisplatin in Patients With Inoperable Esophageal Cancer
Sponsor: Sanofi
Organization: Sanofi

Study Overview

Official Title: Phase II Study Comparing Radiochemotherapy With the Folfox 4 Regimen Versus Radiochemotherapy With 5FU-Cisplatin Herskovic Regimen in First Line Treatment of Patients With Inoperable Esophageal Cancer
Status: COMPLETED
Status Verified Date: 2009-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The primary objectives of this study are to assess the feasibility completion of full treatment in both arms and to assess endoscopic complete response rate in both arms

The secondary objective of this study is to assess the toxicity profile of each arm using the National Cancer Institute-Common Toxicity Criteria NCI-CTC scale V3
Detailed Description: None

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