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Clinical Trial Summary

The purpose of this study is to determine the pathological complete response rate of addition of bevacizumab to induction therapy (xelox) and concomitant treatment (capecitabine+radiotherapy), followed by surgery.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00557713
Study type Interventional
Source Associacio catalana per a la recerca oncologica i les seves implicacions sanitaries i socials
Contact
Status Recruiting
Phase Phase 2
Start date February 2007
Completion date October 2013

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