Viewing Study NCT01871363



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Last Modification Date: 2024-10-26 @ 11:08 AM
Study NCT ID: NCT01871363
Status: UNKNOWN
Last Update Posted: 2013-06-06
First Post: 2013-05-19

Brief Title: Phase II Study of Preoperative IMRT Combined With Capecitabine and Bevacizumab in Locally Advanced Rectal Cancer
Sponsor: Chinese Academy of Medical Sciences
Organization: ChineseAMS

Study Overview

Official Title: Phase II Study of Preoperative IMRT Combined With Capecitabine and Bevacizumab in Locally Advanced Rectal Cancer
Status: UNKNOWN
Status Verified Date: 2013-06
Last Known Status: RECRUITING
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: Pathological complete response pCR correlates with a favourable overall prognosis in locally advanced rectal cancer patients underwent preoperative chemoradiation so obtaining a pCR might be beneficial The aim of the study is to investigate safety and efficacy of preoperative IMRT combined with bevacizumab and capecitabine primary endpoint is pathological complete remission rate
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