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Clinical Trials in China / NCT07256756
Recruiting Phase 1

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

NCT07256756 · tracked via the Priya Life Science China tracker
Sponsor
Shanghai Juncell Therapeutics
Phase
Phase 1
Started
2026-01-30
Last updated
2026-08-05

Condition(s) studied

Solid Tumors, Adult

Investigational drug(s) / intervention(s)

GC203 TIL

GC203 TIL: A tumor sample is resected from each participant and cultured ex vivo to expand the population of engineered tumor infiltrating lymphocytes injection (GC203 TIL). After lymphodepletion, patients are infused GC203 TIL.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
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 regimens, and be willing to receive engineered GC203 TIL therapy; * At least 1 evaluable tumor lesion; Exclusion Criteria: * with other malignant tumors,except for the malignancies that have been cured, have been inactive for ≥5 years prior to study inclusion and have a very low risk of recurrence; Non-melanoma skin cancer or malignant lentigo with adequate treatment and no evidence of disease recurrence; Carcinoma in situ with adequate treatment and no evidence of disease recurrence; * Need glucocorticoid treatment, and daily dose of Prednisone greater than 10mg(or equivalent doses of hormones) or outoimmune diseases requiring immunomodulatory treatment; * Breathe indoor air in a quiet state, and the oxygen saturation of finger pulse is \< 95%; * Human immunodeficiency virus (HIV) infection or anti-HIV antibody positive, active HBV or HCV infection (HBsAg positive and/or anti-HCV positive), syphilis infection or Treponema pallidum antibody positive; * Significant cardiovascular anomalies

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Shenzhen Hospital of Southern Medical University Shenzhen China Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07256756 on ClinicalTrials.gov ↗ ← All trials in China