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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Jose-Luis Garcia +34 663 36 34 24
PASS@eusapharma.com


Study Location:

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Be Part of Research - Trial Details - A Post-Authorisation Safety Study Patient Registry of Patients With Neuroblastoma Being Treated With Dinutuximab Beta

A Post-Authorisation Safety Study Patient Registry of Patients With Neuroblastoma Being Treated With Dinutuximab Beta

Recruiting

Open to: ALL

Age: 1.0 - 18.0

Medical Conditions

Neuroblastoma


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


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.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Sep 2019 Mar 2032

OBSERVATIONAL

Intervention Type : OTHER
Intervention Description : Data will be collected on dose, total cumulative amount of dinutuximab beta per course, dose interruptions, dose discontinuations, prophylactic treatment, use of all concomitant analgesia, assessments of pain, and occurrence of neurotoxicity, visual impairment, capillary leak syndrome, cardiovascular events and hypersensitivity reactions and other AEs.




You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Birmingham Children's Hospital
    Birmingham
    B4 6NH
  • University Hospital Southampton
    Southampton
    SO16 6YD
  • The Newcastle upon Tyne Hospitals NHS Foundation Trust
    Newcastle Upon Tyne
    Newcastle
    NE1 4LP


The study is sponsored by EusaPharma (UK) Limited and is in collaboration with United BioSource, LLC.




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Read full details for Trial ID: NCT04253015
Last updated 06 February 2024

This page is to help you find out about a research study and if you may be able to take part

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