NCT03874897

An Open Label, Single/Multiple Dose Exploratory Clinical Study to Evaluate the Safety, Efficacy, and Cytokinetics of Autologous Humanized Anti-claudin18.2 Chimeric Antigen Receptor T Cell in Advanced Solid Tumor Subjects

Study Summary

An open label, single/multiple dose exploratory clinical study to evaluate the safety, efficacy, and pharmacokinetics of autologous humanized anti-claudin18.2 chimeric antigen receptor T cell in advanced solid tumor.

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Interventions

CAR-CLDN18.2 T-CellsDRUG
Preconditioning with fludarabine, cyclophosphamide, based chemotherapy regimen at sub-clinical doses • Chimeric Antigen Receptor T Cells Targeting Claudin18.2
PD-1 Monoclonal AntibodyDRUG
Chimeric Antigen Receptor T Cells Targeting Claudin18.2 with PD-1
ChemotherapyDRUG
First-line systemic therapy according to physician's choice

Study Locations

FacilityCityStateCountry
Department of GI Oncology, Peking University Cancer HospitalBeijingBeijing MunicipalityChina
The First Affiliated Hospital of Zhengzhou UniversityZhengzhouHenanChina
The First Affiliated Hospital , Zhejiang University School of MedicineHangzhouZhejiangChina

Official Trial Information

View on ClinicalTrials.gov

Data sourced from ClinicalTrials.gov. Last updated: April 14, 2026