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Clinical Trial Summary

This is an interventional, randomized open-label, parallel-group, multicenter, dose escalation phase Ib/II study, to investigate the combination of Regorafenib and XELOX as 2nd line treatment in mCRC patients.


Clinical Trial Description

This is a phase Ib/II trial, comprising Phase Ib and Phase II two parts. Phase Ib study is an open-label, single-arm, multicenter, dose escalation study of Regorafenib plus XELOX. In Phase Ib, max 15 patients(pts) could be enrolled based on the modified toxicity probability interval (mTPI) design. Phase II study is a randomized, open-label, parallel-group, multicenter study comparing Regorafenib + XELOX to XELOX alone. In phase II trial, a total of 39 patients will be recruited and randomized 2:1 into two groups, where 26 patients under Regorafenib + XELOX, and 13 patients under XELOX alone. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04008511
Study type Interventional
Source China Medical University, China
Contact Yunpeng Liu, M.D.,Ph.D.
Phone 86-24-83282312
Email cmu_trial@163.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date July 2019
Completion date March 2024

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