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OncoMatch/Clinical Trials/NCT07502287

Dual-Target GD2/B7-H3 CAR-NK Cells for Pediatric Relapsed or Refractory Neuroblastoma

Is NCT07502287 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies multiple treatments including EB-DTNB-NK and Fludarabine for relapsed neuroblastoma.

Phase 1/2RecruitingBeijing BiotechNCT07502287Data as of Jun 2026Location: China

Treatment: EB-DTNB-NK · Fludarabine · CyclophosphamideThis illustrative Phase 1/Phase 2 study tests allogeneic dual-target GD2/B7-H3 (CD276) CAR-NK cells in children and young adults with relapsed or refractory neuroblastoma. After lymphodepletion, participants receive IV CAR-NK cells;Part A defines the RP2D and Part B estimates preliminary activity

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Extracted eligibility criteria

Treatments studied

Chemotherapy

FludarabineCyclophosphamide

Other

EB-DTNB-NK

Cancer type

Neuroblastoma

Biomarker criteria

Required: GD2 expression (positive)

Tumor material available for central assessment of GD2 and B7-H3 expression; at least one target must be positive

Required: CD276 expression (positive)

Tumor material available for central assessment of GD2 and B7-H3 expression; at least one target must be positive

Demographics

Ages 1–21

Prior therapy

Must have received: standard neuroblastoma therapy

Prior exposure to standard neuroblastoma therapy, including anti-GD2-based therapy, unless contraindicated, unavailable, or declined for a documented medical reason

Cannot have received: genetically modified cellular therapy

Prior genetically modified cellular therapy within the protocol-defined washout window

Lab requirements

Blood counts

adequate hematologic function considered sufficient by protocol-defined laboratory and clinical thresholds

Kidney function

adequate renal function considered sufficient by protocol-defined laboratory and clinical thresholds

Liver function

adequate hepatic function considered sufficient by protocol-defined laboratory and clinical thresholds

Cardiac function

adequate cardiac function considered sufficient by protocol-defined laboratory and clinical thresholds

Adequate organ function: hematologic, renal, hepatic, cardiac, and pulmonary function considered sufficient by protocol-defined laboratory and clinical thresholds

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07502287 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior genetically modified cellular therapy disqualifies patients from enrollment.

Does this trial require GD2?

Yes, GD2 expression is a required biomarker for enrollment.

Does this trial require CD276?

Yes, CD276 expression is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 21 years or younger and at least 1 years old.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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