drugset / Trial / NCT03240861

Genetically Engineered PBMC and PBSC Expressing NY-ESO-1 TCR After a Myeloablative Conditioning Regimen to Treat Patients With Advanced Cancer

NCT03240861

NaSingle-groupOpen-labelTreatment

Summary

This phase I clinical trial evaluates the safety and feasibility of administering NY-ESO-1 TCR (T cell receptor)engineered peripheral blood mononuclear cells (PBMC) and peripheral blood stem cells (PBSC) after a myeloablative conditioning regimen to treat patients with cancer that has spread to other parts of the body. The conditioning chemotherapy makes room in the patient?s bone marrow for new blood cells (PBMC) and blood-forming cells (stem cells) to grow. Giving NY-ESO-1 TCR PBMC and stem cells after the conditioning chemotherapy is intended to replace the immune system with new immune cells that have been redirected to attack and kill the cancer cells and thereby improve immune system function against cancer.

Timeline

Start
2017-07-26
Primary completion
2023-10-19
Completion
2023-10-19

Drugs

EvaluationDrugModalityDoseRoute
Subject LV-NYESO TCR/sr39TK PBSC Unknown Intravenous
Subject RV-NYESO TCR PBMC Cell therapy Intravenous
Background Busulfan Small molecule Intravenous
Background Fludarabine Small molecule Intravenous
Background Plerixafor Small molecule Subcutaneous
Background aldesleukin Protein / enzyme biologic Subcutaneous
Background filgrastim Protein / enzyme biologic Subcutaneous