drugset / Trial / NCT06889766

NY-ESO-1-redirected T Cells in Patients With Advanced Melanoma and Sarcoma

NCT06889766 ↗

Phase 1 Recruiting 9 enrolled Centre Hospitalier Universitaire Vaudois
NaSingle-groupOpen-labelTreatment

Summary

A single center, dose escalaion, Phase I clinical trial to demonstrate safety and efficacy of LauT-1, autologous "New York Esophageal Squamous Cell Carcinoma-1 T-Cell Receptor (NY-ESO-1 TCR)-directed T cells in combination with non-myeloablative (NMA) lymphodepleting chemotherapy and low dose irradiation (LDI) in patients with NY-ESO-1 positive sarcoma and melanoma.

Timeline

Start
2025-03-24
Primary completion
2029-06
Completion
2029-06

Drugs

EvaluationDrugModalityDoseRoute
Subject LauT-1 Cell therapy 3e+08 cells Intravenous
Subject LauT-1 Cell therapy 6e+08 cells Intravenous
Subject LauT-1 Cell therapy 2e+09 cells Intravenous
Background Cyclophosphamide Other / unclassified 900 mg/m2 Intravenous
Background Cyclophosphamide Other / unclassified 1800 mg/m2 Intravenous
Background Cyclophosphamide Other / unclassified 2400 mg/m2 Intravenous
Background Fludarabine Small molecule 30 mg/m2 Intravenous