drugset / Trial / NCT02650986

Gene-Modified T Cells With or Without Decitabine in Treating Patients With Advanced Malignancies Expressing NY-ESO-1

NCT02650986

Phase 1/2 Active not recruiting 15 enrolled Roswell Park Cancer Institute National Cancer Institute (NCI) · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

This phase I/IIa trial studies the side effects and best dose of gene-modified T cells when given with or without decitabine, and to see how well they work in treating patients with malignancies expressing cancer-testis antigens 1 (NY-ESO-1) gene that have spread to other places in the body (advanced). A T cell is a type of immune cell that can recognize and kill abnormal cells of the body. Placing a modified gene for NY-ESO-1 into the patients' T cells in the laboratory and then giving them back to the patient may help the body build an immune response to kill tumor cells that express NY-ESO-1. Drugs used in chemotherapy, such as decitabine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. It is not yet known whether giving gene-modified T cells with or without decitabine works better in treating patients with malignancies expressing NY-ESO-1.

Timeline

Start
2017-07-14
Primary completion
2021-03-04
Completion
2032-07-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Decitabine Small molecule Intravenous
Subject TGFbDNRII-transduced Autologous Tumor Infiltrating Lymphocytes Cell therapy Intravenous
Background Cyclophosphamide Other / unclassified Intravenous