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

RecruitingPhase 1Ages 18 Years - 75 YearsAllXiangdong Cheng
NCT06610799 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Male or female subjects, ≥ 18 years and ≤75 years. 2. Subjects with unresectable advanced or metastatic gastric and gastroesophageal junction adenocarcinoma without prior systematic treatment. 3. Subjects with at least one measurable lesion according to RECIST v1.1. 4. Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1. 5. Expected survival time ≥ 3 months. Exclusion Criteria: 1. Women who are pregnant or lactating, or intending to become pregnant before, during, or within 6 months after the last dose of study drug. 2. Active uncontrolled bleeding or a known bleeding diathesis. 3. Subjects with history of or known active seizure disorder, brain metastases, spinal cord compression, or carcinomatous meningitis, or new evidence of brain or leptomeningeal disease.
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What it tests

  • IBI363
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Where

1 site
Zhejiang Cancer Hospital
Hangzhou, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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