drugset / Trial / NCT03967223

Master Protocol to Assess the Safety and Antitumor Activity of Genetically Engineered T Cells in NY-ESO-1 and/or LAGE-1a Positive Solid Tumors

NCT03967223 ↗

Phase 2 Active not recruiting 103 enrolled USWM CT, LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This trial will evaluate safety and efficacy of human engineered T-cell therapies, in participants with advanced tumors.

Timeline

Start
2019-12-31
Primary completion
2024-03-01
Completion
2026-07-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Letetresgene autoleucel Cell therapy — —
Background Cyclophosphamide Other / unclassified — —
Background Fludarabine Small molecule — —

Indications