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Study identifier: NCT04023331 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Terminated

67Cu-SARTATE™ Peptide Receptor Radionuclide Therapy Administered to Pediatric Patients With High-Risk, Relapsed, Refractory Neuroblastoma

Condition: Neuroblastoma · Relapsed Neuroblastoma · Refractory Neuroblastoma  ·  Sponsor: Clarity Pharmaceuticals Ltd

PhasePhase 1/Phase 2
Planned participants21
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The aim of this study is to evaluate the safety and efficacy of 67Cu-SARTATE in pediatric patients with high-risk neuroblastoma.

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

Talk to the study team

No contact information is available for this study as per the public registry record.

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Locations (8)

Phoenix Children's HospitalPhoenix, Arizona, United States
Washington University School of MedicineSt Louis, Missouri, United States
Memorial Sloan Kettering Cancer CenterNew York, New York, United States
Cincinnati Children's Hospital Medical CentreCincinnati, Ohio, United States
Medical University of South CarolinaCharleston, South Carolina, United States
University of Texas Southwestern Medical CentreDallas, Texas, United States
MD Anderson Cancer CenterHouston, Texas, United States
University of WisconsinMadison, Wisconsin, United States

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