Clinical study - Pédiatrie Neuroblastomes

EUSA-PASS (EUSA-DB-0001)
Pédiatrie Neuroblastomes
Ouvert depuis le: 04.24.2024
Site: Paris
Public cible
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A Post-Authorisation Safety Study Patient Registry of Patients With High-risk Neuroblastoma Being Treated With the Monoclonal Antibody Dinutuximab Beta
Description de l'essai
This is a non-interventional, multi-national, observational, prospective patient registry to further evaluate the effectiveness and safety of dinutuximab beta - a monoclonal immunoglobulin G 1 (IgG1) antibody, to obtain information on survival, pain severity and incidence of neuro-toxicity, visual impairment, capillary leak syndrome, cardiovascular events, hypersensitivity reactions and long-term safety.
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GUDRUN SCHLEIERMACHER
Investigateur principal