Overview
A Study of the Effect of Hu3F8/GM-CSF Immunotherapy Plus Isotretinoin in Patients in First Remission of High-Risk Neuroblastoma
Status:
Active, not recruiting
Active, not recruiting
Trial end date:
2022-06-01
2022-06-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to test see the combined effects of the study drug called Humanized 3F8 (Hu3F8) when used with granulocyte-macrophage colony stimulating factor (GM-CSF). Hu3F8 plus GM-CSF could prevent your neuroblastoma from growing, but it could also cause side effects.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Memorial Sloan Kettering Cancer CenterCollaborator:
Y-mAbs TherapeuticsTreatments:
Isotretinoin
Criteria
Inclusion Criteria:- Diagnosis of NB as defined by a) histopathology (confirmed by the MSK Department of
Pathology), or b) BM metastases or MIBG-avid lesion(s) plus high urine catecholamine
levels.
- Patients must have high-risk NB (MYCN-amplified stage 2/3/4/4S of any age and
MYCN-nonamplified stage 4 in patients greater than 18 months of age).
- Patients must be in first CR/VGPR
- Patients must have a negative human anti-hu3F8 antibody (HAHA) titer
Exclusion Criteria:
- Existing major organ dysfunction, i.e., renal., cardiac, hepatic, neurologic,
pulmonary, or gastrointestinal toxicity ≥ grade 3, with the exception of hearing loss
and hematologic toxicity.
- Active life-threatening infection.
- Inability to comply with protocol requirements