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Clinical Trial Summary

The purpose of this study is to evaluate the safety, tolerability, and efficacy of JX-594 (Pexa-Vec) administered intravenously either alone or in combination with Irinotecan in colorectal carcinoma patients who are refractory to or intolerant to standard therapy.


Clinical Trial Description

This was a Phase 1/2a, open-label, dose-escalation study in patients with advanced colorectal cancer (CRC) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01394939
Study type Interventional
Source SillaJen, Inc.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date January 2012
Completion date October 2015

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