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Clinical Trial Summary

The purpose of this study is to compare OnDose® based pharmacokinetic administration of 5-FU versus standard Body Surface Area (BSA) based administration of 5-FU in patients with metastatic colorectal cancer treated with mFOLFOX6, with or without bevacizumab, to determine if the use of OnDose® achieves an improvement in the Overall Response Rate (ORR) relative to BSA dosing response.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01468623
Study type Interventional
Source Myriad Genetic Laboratories, Inc.
Contact
Status Terminated
Phase Phase 4
Start date September 2011
Completion date August 2012