CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 41 enrolled
Drug / intervention
Dinutuximab +12 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04385277
NCT04385277Phase 2Active

A Pilot Study of Dinutuximab, Sargramostim (GM-CSF), and Isotretinoin in Combination With Irinotecan and Temozolomide in the Post-Consolidation Setting for High-Risk Neuroblastoma

Children's Oncology Group·interventional·Posted May 12, 2020·Updated Oct 27, 2025

In Brief

A Phase 2 clinical trial evaluating Biospecimen Collection, Bone Marrow Aspiration, and 11 other interventions for Ganglioneuroblastoma, Nodular and Neuroblastoma. Active but no longer recruiting, targeting 41 participants across 77 sites in 4 countries.

Detailed Summary

This phase II trial studies if dinutuximab, GM-CSF, isotretinoin in combination with irinotecan, and temozolomide (chemo-immunotherapy) can be given safely to patients with high-risk neuroblastoma after Consolidation therapy (which usually consists of two autologous stem cell transplants and radiation) who have not experienced worsening or recurrence of their disease. Dinutuximab represents a kind of cancer therapy called immunotherapy. Unlike chemotherapy and radiation, dinutuximab targets the cancer cells without destroying nearby healthy cells. Sargramostim helps the body produce normal infection-fighting white blood cells. Isotretinoin helps the neuroblastoma cells become more mature. These 3 drugs (standard immunotherapy) are already given to patients with high-risk neuroblastoma after Consolidation because they have been proven to be beneficial in this setting. Chemotherapy drugs, such as irinotecan and temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. They may also affect how well immunotherapy works on neuroblastoma cells. Giving chemo-immunotherapy after intensive therapy may work better in treating patients with high-risk neuroblastoma compared to standard immunotherapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Canada, New Zealand, United States

Timeline

Phase 2Active
2021202220232024202520262027
First PostedMay 12, 2020
Enrollment StartDec 31, 2020
Primary CompletionJun 30, 2023
Study CompletionSep 30, 2027
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 6.1 years ago

Interventions

Biospecimen Collectionprocedure

Correlative studies

Bone Marrow Aspirationprocedure

Undergo BM aspiration

Bone Marrow Biopsyprocedure

Undergo BM biopsy

Computed Tomographyprocedure

Undergo CT

Dinutuximabbiological

Given IV

FDG-Positron Emission Tomographyprocedure

Undergo FDG-PET

Iobenguane I-123radiation

Undergo 123I-MIBG

Irinotecandrug

Given IV

Isotretinoindrug

Given PO

Magnetic Resonance Imagingprocedure

Undergo MRI

Multigated Acquisition Scanprocedure

Undergo MUGA

Sargramostimbiological

Given SC or IV

Temozolomidedrug

Given PO or via enteral tube