drugset / Trial / NCT03017131

Genetically Modified T Cells and Decitabine in Treating Patients With Recurrent or Refractory Ovarian, Primary Peritoneal, or Fallopian Tube Cancer

NCT03017131 ↗

NaSingle-groupOpen-labelTreatment

Summary

This phase I trial studies the side effects of genetically modified T cells and decitabine in treating patients with recurrent or refractory epithelial or non-epithelial ovarian, primary peritoneal, or fallopian tube cancer that has come back or has not responded to previous treatments. White blood cells called T cells are collected via a process called leukapheresis, genetically modified to recognize and attack tumor cells, then given back to the patient. Decitabine may induce and increase the amount of the target protein NY-ESO-1 available on the surface of tumor cells. Giving genetically modified T cells and decitabine may kill more tumor cells.

Timeline

Start
2017-12-08
Primary completion
2020-03-23
Completion
2032-03-23

Drugs

EvaluationDrugModalityDoseRoute
Subject Decitabine Small molecule — Intravenous
Subject Genetically Engineered NY-ESO-1-specific T Lymphocytes Cell therapy — Intravenous
Background Cyclophosphamide Other / unclassified — Intravenous
Background aldesleukin Protein / enzyme biologic — Subcutaneous