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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Request More InfoInterventions
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
| Facility | City | State | Country |
|---|---|---|---|
| Department of GI Oncology, Peking University Cancer Hospital | Beijing | Beijing Municipality | China |
| The First Affiliated Hospital of Zhengzhou University | Zhengzhou | Henan | China |
| The First Affiliated Hospital , Zhejiang University School of Medicine | Hangzhou | Zhejiang | China |