NCT02498912

A Phase I Clinical Trial of Cyclophosphamide Followed by Intravenous and Intraperitoneal Infusion of Autologous T Cells Genetically Engineered to Secrete IL-12 and to Target the MUC16ecto Antigen in Patients With Recurrent MUC16ecto+ Solid Tumors

Study Summary

The purpose of this phase I study is to test the safety of different dose levels of specially prepared cells collected called "modified T cells". In the screening part of this study the tumor was found to have a protein called MUC16. This protein is present on about 70% of ovarian cancers. The investigators want to find a safe dose of modified T cells for patients with this type of cancer that has progressed after standard chemotherapy. We also want to find out what effects these modified T cells have on the patient and their cancer.

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Interventions

Production of Genetically-modified T cellsPROCEDURE
No description available.
CyclophosphamideDRUG
No description available.
IP Catheter InsertionDEVICE
No description available.
Infusion of 4H11-28z/fIL-12/EGFRt+ Genetically-modified T cellsGENETIC
Patients who do not have sufficient CAR T cells for the assigned dose cohort will be treated in the cohort for which cells are available.
FludarabineDRUG
fludarabine dose 25-30 mg/m2 x 3 days

Study Locations

FacilityCityStateCountry
Memorial Sloan Kettering Cancer CenterNew YorkNew YorkUnited States

Official Trial Information

View on ClinicalTrials.gov

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