Clinical Research Directory
Browse clinical research sites, groups, and studies.
Perioprative Study of IBI363 in Patients With MHC-II-Negative Locally Advanced Gastric Cancer
Sponsor: Zhejiang Cancer Hospital
Summary
This is a phase 2 study designed to evaluate the safety and efficacy of IBI363 in combination with oxaliplatin and capecitabine (XELOX) or S-1 and oxaliplatin (SOX) in perioprative treatment of locally advanced MHC-II-negative gastric and gastroesophageal junction adenocarcinoma.
Official title: IBI363 Combined Chemotherapy for Perioperative Treatment of MHC-II-Negative Locally Advanced Gastric/Gastroesophageal Junction Adenocarcinoma: A Single-Center, Single-Arm Phase II Clinical Study
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
60
Start Date
2025-11-03
Completion Date
2027-12-31
Last Updated
2026-01-08
Healthy Volunteers
No
Conditions
Interventions
IBI363 + chemotherapy
IBI363 Q3W +XELOX Q3W (Oxaliplatin 130 mg/m2, IV, Q3W, Capecitabine ,1000mg/ m2, PO, Bid, d1-14, Q3W) or IBI363 Q3W +SOX (Oxaliplatin 130 mg/m2, IV, Q3W, S-1, 40-60mg,PO, Bid, d1-14,Q3W )
Locations (1)
Zhejiang Cancer Hospital
Hangzhou, Zhejiang, China