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Clinical Trial Summary

This study is to investigate the safety and efficacy on TIL engineered with membrane-binding cytokine (GC203 TIL) for the treatment of patients with advanced gynecologic tumors. Autologous TILs from tumor resections or biopsies are first gene modified (engineered with membrane-binding cytokine) and than expanded before i.v. infusion into the patient after NMA lymphodepletion treatment with cyclophosphamide.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05468307
Study type Interventional
Source Shanghai Juncell Therapeutics
Contact Clinical GC
Phone 086-18001759113
Email clinicaltrials@juncell.com
Status Recruiting
Phase Early Phase 1
Start date March 10, 2022
Completion date March 10, 2025

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