drugset / Trial / NCT06610799

Study of IBI363 in Patients with Advanced First-line Gastric Cancer

NCT06610799

Phase 1 Recruiting 40 enrolled Xiangdong Cheng
NaSingle-groupOpen-labelTreatment

Summary

This is a phase 1b study designed to evaluate the safety, tolerability and efficacy of IBI363 in combination with oxaliplatin and capecitabine (XELOX) in first-line treatment of unresectable advanced or metastatic gastric and gastroesophageal junction adenocarcinoma.

Timeline

Start
2024-10-15
Primary completion
2025-06-30
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject IBI363 Protein / enzyme biologic
Background Capecitabine Small molecule 1000 mg/m2 Oral
Background Oxaliplatin Small molecule 130 mg/m2 Intravenous

Indications

No indication recorded.