RecruitingPhase 1Phase 2NCT07193966

NG2 and DLL3 CAR-T Cells Targeting Melanoma

Safety and Efficacy of NG2 and DLL3 CAR-T Therapy Targeting Melanoma


Sponsor

Shenzhen Geno-Immune Medical Institute

Enrollment

100 participants

Start Date

Sep 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to assess the feasibility, safety and efficacy of multiple CAR-T cell therapy which targets NG2 and DLL3 surface antigens in patients with relapsed and refractory melanoma.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing CAR-T cell therapy — immune cells engineered to target two proteins (NG2 and DLL3) found on melanoma and other cancers — in patients whose cancer has progressed after standard first-line treatment. **You may be eligible if...** - You are between 18 and 75 years old - You have a confirmed tumor that expresses NG2 and/or DLL3 proteins (tested by biopsy) - Your cancer is non-resectable, metastatic, progressive, or recurrent - You have already received and progressed on standard first-line treatment - You weigh at least 40 kg and have a life expectancy of at least 8 weeks - Any serious side effects from prior treatments have resolved to grade 2 or lower **You may NOT be eligible if...** - Your tumor does not express NG2 or DLL3 - You have not yet received first-line therapy - You have recently had a stem cell or bone marrow transplant - Your weight is below 40 kg or life expectancy is under 8 weeks Talk to your doctor to see if this trial is right for you.

This is a simplified summary. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interventions

BIOLOGICALNG2 and DLL3 CAR-T cells

Infusion of NG2 and DLL3-specific CAR-T via intravenous route


Locations(1)

Shenzhen Geno-immune Medical Institute

Shenzhen, Guangdong, China

View Full Details on ClinicalTrials.gov

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NCT07193966


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