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Study identifier: NCT07549321 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Safety and Efficacy Study of hu14 in High-Risk Neuroblastoma Patients

Condition: High-Risk Neuroblastoma  ·  Sponsor: Renaissance Pharma Ltd.

PhasePhase 2/Phase 3
Planned participants144
Who can joinAll sexes, 18 Months to 18 Years
Healthy volunteersNo

About this study

Neuroblastoma is the most common type of solid cancer found outside the brain in young children. Generally, it affects children younger than 5 years old, with the average age when it is found being just 2 years. Most patients have 'high-risk' disease, with spread of the disease to different sites (metastases). This multinational study aims to find out how effective and safe the treatment of a monoclonal anti-GD2 antibody hu14.18K322A (daretabart) is when used together with chemotherapy to treat children and young people who have high-risk neuroblastoma.

This description comes directly from the study's public registry record.

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Contact details are listed per location below or on the registry record.

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Locations (5)

Children's Hospital Colorado Anschutz MedicalAurora, Colorado, United StatesRecruiting
University of Minnesota Masonic Children's HospitalMinneapolis, Minnesota, United StatesRecruiting
The Children's Hospital at MontefioreThe Bronx, New York, United StatesRecruiting
Duke University Medical CenterDurham, North Carolina, United StatesRecruiting
Children's Hospital of PhiladelphiaPhiladelphia, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07549321