Viewing Study NCT00137878



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Last Modification Date: 2024-10-26 @ 9:13 AM
Study NCT ID: NCT00137878
Status: COMPLETED
Last Update Posted: 2012-02-23
First Post: 2005-08-26

Brief Title: TNFerade Plus ChemoRadiationSurgery for Rectal Cancer
Sponsor: GenVec
Organization: GenVec

Study Overview

Official Title: A Phase II Randomized Trial Comparing TNFerade Biologic With Capecitabine and Radiation Therapy Followed by Surgical Resection Versus Capecitabine and Radiation Therapy Followed by Surgical Resection for the Treatment of Rectal Cancer
Status: COMPLETED
Status Verified Date: 2011-05
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 if the addition of TNFerade to pre-operative chemoradiotherapy increases the number of pathologic complete responses when compared to pre-operative chemoradiotherapy alone as assessed following complete surgical resection of primary rectal cancer
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