Last updated on August 2019

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


Brief description of study

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.

Detailed Study Description

This is a multi-center, non-randomized, open-label study in patients with high-risk neuroblastoma to assess the immunogenicity, safety and tolerability of Unituxin combination therapy. Patients enrolled in the study were prescribed Unituxin for the treatment of high-risk neuroblastoma.

Clinical Study Identifier: NCT02693171

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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