A Study of GC203 TIL in Advanced Solid Tumors (NF)

Recruiting Phase 1 Interventional Study
Solid Tumors, Adult
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
8 (estimated)
Sponsor
Shanghai Juncell Therapeutics · Industry
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About This Trial

This study is a prospective, open-label, single-arm clinical trial aimed at evaluating the safety and efficacy of GC203 TIL therapy in treating malignant solid tumors that have failed standard treatment.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * have one the tumor resection for gene-edited GC203 TIL production and successfully produced; * Age: 18 years to 75years; * Histologically diagnosed as solid tumor; * Expected life-span more than 3 months; * ECOG score 0-1; * Test subjects have failed standard treatment regimen…
Contacts

Ying Cheng

+8621-69110327

ying.cheng@juncell.com

CONTACT