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
Trial end date:
2022-06-01
Target enrollment:
0
Participant gender:
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 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Memorial Sloan Kettering Cancer Center
Collaborator:
Y-mAbs Therapeutics
Treatments:
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