606
Participants
Start Date
August 14, 2023
Primary Completion Date
December 1, 2025
Study Completion Date
December 1, 2026
HR070803 plus oxaliplatin, 5-FU/LV, bevacizumab
HR070803 plus oxaliplatin, 5-FU/LV, bevacizumab Patients will receive the study drug after randomization, and those with effective efficacy evaluation (CR, PR or SD) will receive intravenous chemotherapy for up to 8-12 cycles, and then enter the maintenance treatment stage until PD, death, intolerable toxicity or withdrawal of informed consent (whichever occurs first)
HR070803 simulator plus oxaliplatin, 5-FU/LV, bevacizumab
HR070803 simulator plus oxaliplatin, 5-FU/LV, bevacizumab Patients will receive the study drug after randomization, and those with effective efficacy evaluation (CR, PR or SD) will receive intravenous chemotherapy for up to 8-12 cycles, and then enter the maintenance treatment stage until PD, death, intolerable toxicity or withdrawal of informed consent (whichever occurs first)
RECRUITING
Sun Yat-Sen University Cancer Center, Guangzhou
Jiangsu HengRui Medicine Co., Ltd.
INDUSTRY