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Clinical Trial Summary

To evaluate the objective response rate, disease control rate, progression-free survival, overall survival, surgical conversion rate and safety of irinotecan liposome combined with 5-FU/LV+ bevacizumab regimen in first-line treatment of advanced metastatic colorectal cancer patients.


Clinical Trial Description

This is a Phase II clinical study to evaluate the efficacy and safety of the combination regimen of irinotecan liposome injection in the first-line treatment of metastatic colorectal cancer. Patients will receive liposomal injections of irinotecan 70mg/m^2 d1, bevacizumab 5mg/kg d1, LV 400mg/m^2 d1, 5-FU 400mg/m^2, then 2400mg/m^2, continuous intravenous infusion for 46-48h, d1-2. 86 eligible patients will be enrolled. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06341296
Study type Interventional
Source West China Hospital
Contact Meng Qiu, MD
Phone 028-85423203
Email qiumeng33@hotmail.com
Status Not yet recruiting
Phase Phase 2
Start date June 2024
Completion date December 2026

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