Humanized CAR-T-mesothelin

Phase 1 Study of Human Chimeric Antigen Receptor Modified T Cells in Patients With Mesothelin Expressing Cancers

Principal Investigator

Phase Penn Study Number Clinicaltrials.gov ID
Janos Tanyi, MD PhD 1 UPCC02916 NCT03054298

Purpose

Phase I study to establish safety and feasibility of intravenous or intrapleural administered lentiviral transduced huCART-meso cells with or without lymphodepletion.  Intravenous administration of huCART-meso cells is planned with or without cyclophosphamide as lymphodepleting chemotherapy.

Check Eligibility For This Trial

To inquire about participating in this study, please contact Kim Shea, RN at 215-222-2222 or Email