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Clinical Trial Summary

The purpose of this study is to examine the use of activated T cells (ATCs) to assess the safety and tolerability of autologous activated T cells, as measured by the number of Grade 3 or higher toxicities, the number of serious adverse events, and treatment-related toxicities, according to National Cancer Institute Common Toxicity Criteria for Adverse Events (NCI CTCAE) Version 5, to find the maximum tolerated dose. The secondary objectives include evaluating the rate of overall survival, rate of progression-free survival, health-related quality of life parameters, overall response rate, immune response, and tumor stem cell antigen expression.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05341947
Study type Interventional
Source Cedars-Sinai Medical Center
Contact Kortnee Calkins
Phone 310-285-7210
Email Kortnee.Calkins@cshs.org
Status Not yet recruiting
Phase Phase 1
Start date June 2022
Completion date June 2025

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