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Clinical Trial Summary

The objective is to evaluate the efficacy and safety of modified XELOXIRI combined with molecular targeted drug as first-line therapy in patients with metastatic colorectal cancer (mCRC)


Clinical Trial Description

It is an investigator-initiated, single institution, prospective, single-arm clinical study to evaluate the efficacy and safety of modified XELOXIRI combined with molecular targeted drug as first-line therapy in patients with unresectable mCRC. Eligible patients will receive 8 cycles of mXELOXIRI with cetuximab or bevacizumab and then the maintenance therapy until disease progression (PD) or unacceptable toxicity, whichever occurs first. Study evaluation time is defined as up to 16 weeks after the first dosing of the last patient. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04160416
Study type Interventional
Source First Affiliated Hospital of Zhejiang University
Contact Jiang F Weiqin, M.D
Phone +86 15068117618
Email 1312028@zju.edu.cn
Status Recruiting
Phase Phase 2
Start date July 1, 2019
Completion date January 1, 2022

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