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Immunotherapy with dinutuximab beta in combination with chemotherapy for the treatment of patients with primary neuroblastoma refractory to standard therapy and with relapsed or progressive disease.

Phase 1
Conditions
Recurrent or progression of neuroblastoma or neuroblastoma or neuroblastoma refractory to first-line treatment.
MedDRA version: 20.0Level: LLTClassification code: 10029261Term: Neuroblastoma NOS Class: 10029104
Therapeutic area: Diseases [C] - Neoplasms [C04]
Registration Number
CTIS2024-513141-37-00
Lead Sponsor
niwersytet Jagiellonski Collegium Medicum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
28
Inclusion Criteria

Diagnosis of NBL according to international criteria (International Neuroblastoma Risk Group, INRG)., Patients 1-18 years of age with HR-NBL with primary refractory disease, disease progression or recurrence., Adequate function of vital organs (if abnormal, dysfunction below grade 4 according to the CTC AE WHO classification, except for disorders defined in the exclusion criteria)., Life expectancy =6 months.

Exclusion Criteria

Patients with toxicities of =3 CTCAE WHO grade, except hearing impairment, hematological disorders, liver and kidney disorders., Patients with neurological toxicities of =2 CTCAE WHO grade., Active life-threatening infection until stabilization of the patient's condition., Pregnancy and / or lactation, Radiotherapy within 3 weeks prior to the start of the study.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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