OncoMatch

OncoMatch/Clinical Trials/NCT07399821

An Imaging Study of Anti-GD2-800CW in Patients With Neuroblastoma

Is NCT07399821 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies anti-GD2-800CW for neuroblastoma.

Phase 1/2RecruitingPrincess Maxima Center for Pediatric OncologyNCT07399821Data as of Jun 2026Location: Netherlands

Treatment: anti-GD2-800CWThis is a non-randomized, open label phase Ib/II dose-escalation and expansion study designed to define the recommended dose of anti-GD2-800CW in pediatric neuroblastoma patients. The aim of this imaging study is to determine a safe and effective dose of anti-GD2-800CW for intra-operative detection of neuroblastoma using NIR fluorescence.

Check if I qualify

Extracted eligibility criteria

Treatments studied

Other

anti-GD2-800CW

Cancer type

Neuroblastoma

Demographics

Ages 1–18

Prior therapy

Cannot have received: anti-GD2 antibody (Dinutuximab-beta)

Previous treatment with Dinutuximab-beta, either alone or in combination with chemotherapy

Cannot have received: chimeric antibody

Patients that received prior treatment with chimeric antibodies

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

Frequently asked questions

Is NCT07399821 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior anti-GD2 antibody, chimeric antibody disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 18 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.

Check if I qualify