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Taking people in United StatesPhase 2

Tests reduced chemotherapy with an antibody treatment for children with neuroblastoma

Tests whether reduced chemotherapy plus an antibody is safe in children with high-risk neuroblastoma.

Plain-language title generated from the registry record
Registry title: N10: A Study of Reduced Chemotherapy and Monoclonal Antibody (mAb)-Based Therapy in Children With Neuroblastoma

Key facts

Where
New York, United StatesSee the site
Phase
Phase 2

Where in United States

  • Memorial Sloan-Kettering Cancer CenterNew York, United StatesTaking people

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  4. What happens if I want to stop?
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Trial details

Who runs it
Memorial Sloan Kettering Cancer Center
Trial code
NCT06528496
Record updated
28 August 2026
Original description
The purpose of this study is to find out whether N10 chemotherapy is a safe and effective treatment for children with high-risk neuroblastoma.Read full original descriptionShow less

N10: Reduced Therapy for High-Risk Neuroblastoma

The purpose of this study is to find out whether N10 chemotherapy is a safe and effective treatment for children with high-risk neuroblastoma.

Inclusion: Diagnosis of NB as defined by histopathology, BM metastases plus high urine catecholamine levels, or positivity in MIBG scan; HR-NB, defined as MYCN-amplified stage L2/M/MS at any age and stage M in patients >18 months old; No more than one prior cycle of HR-NB chemotherapy; Age <19 years; Signed informed consent indicating awareness of the investigational nature of this treatment.

Exclusion: Severe dysfunction of major organs, i.e., renal, cardiac, hepatic, neurologic, pulmonary, hematologic, or gastrointestinal toxicity >/= to grade 3; °Organ dysfunction due to direct effects of primary tumor or metastatic disease, or due to paraneoplastic syndromes associated with neuroblastoma, will not be considered in exclusion criteria. Similarly, complications of interventions to control above direct effects (e.g., steroid- induced hyperglycemia or hypertension) will also not be considered in exclusion criteria; Inability to comply with protocol requirements; Pregnancy.

ClinicalTrials.gov NCT06528496