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Clinical Trial Detail

Post-Marketing Assessment of Immunogenicity and Safety of Unituxin™ in High-Risk Neuroblastoma Patients

Complete title: SC-4011, A Post-Marketing Study to Further Assess the Immunogenicity and Safety of UnituxinTM in High-Risk Neuroblastoma Patients

Research Study Number SC-4011
Principal Investigator Julie Park, MD
Phase IV

Research Study Description

The purpose of this study is to assess the incidence of human anti-chimeric antibody (HACA) in high-risk neuroblastoma patients treated with Unituxin combination therapy.

Eligibility Criteria (must meet the following to participate in this study)

** For Eligibility information, please click on the "Look up trial at NIH" link above. **

Other eligibility criteria may apply.

Research Study Number SC-4011
Contact Julie Park, MD
Telephone 206/667-1212

Keywords: Neuroblastoma; Neuroectodermal Tumors, Primitive (PNET); Solid Tumors; Neoplasms, Germ Cell and Embryonal; Neuroectodermal Tumors; Neoplasms, Glandular and Epithelial; Neoplasms, Nerve Tissue; Neoplasms, Neuroepithelial

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