762
Participants
Start Date
May 30, 2025
Primary Completion Date
December 31, 2028
Study Completion Date
April 30, 2030
HS-10370
Participants will receive HS-10370 dose 1 administered orally
HS-20117
Participants will receive HS-20117 given as dose 3 intravenous infusion(IV) once every 14-day cycle.
Adebrelimab
Participants will receive Adebrelimab intravenous infusion(IV) once every 21-day cycle
Capecitabine
Participants will receive Capecitabine administered orally
Oxaliplatin
Participants will receive Oxaliplatin intravenous infusion(IV) once every 21-day cycle.
Folinic Acid, Fluorouracil and Oxaliplatin/Irinotecan
Participants will receive Folinic Acid, Fluorouracil and Oxaliplatin/Irinotecan intravenous infusion(IV) once every 14-day cycle.
HS-20093
Participants will receive HS-20093 intravenous infusion(IV) once every 21-day cycle
platinum (cisplatin or carboplatin)
Participants will receive platinum (cisplatin or carboplatin) administered IV in 21-day cycles.
The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou
Sun Yat-sen University Cancer Center, Shanghai
Lead Sponsor
Jiangsu Hansoh Pharmaceutical Co., Ltd.
INDUSTRY