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Radioactive Agent
hematopoietic stem cell infusion for Neuroblastoma
N/A
Waitlist Available
Led By Emily Greengard, MD
Research Sponsored by Masonic Cancer Center, University of Minnesota
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
Study Summary
This trial is testing a new therapy for neuroblastoma and pheochromocytoma, two cancer types that are difficult to treat. The trial will evaluate how well the therapy works and how safe it is.
Eligible Conditions
- Neuroblastoma
- Pheochromocytoma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of patients who receive 131 I-MIBG.
Secondary outcome measures
Disease response
Improvement of fatigue
Pain
+3 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: 131 I-MIBG Treatment ArmExperimental Treatment4 Interventions
Therapeutic 131 I-Metaiodobenzylguanidine (131I-MIBG) will be infused intravenously, intravenous fluids will be administered to help maintain urine flow and isotope excretion. Potassium iodide solution will be administered to protect thyroid function. G-CSF will be used if necessary for neutrophil recovery. Hematopoietic stem cell infusion if meets the criteria.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
G-CSF
2014
Completed Phase 4
~1610
Find a Location
Who is running the clinical trial?
Masonic Cancer Center, University of MinnesotaLead Sponsor
271 Previous Clinical Trials
14,525 Total Patients Enrolled
4 Trials studying Neuroblastoma
42 Patients Enrolled for Neuroblastoma
Emily Greengard, MDPrincipal InvestigatorUniversity of Minnesota Department of Pediatrics
Frequently Asked Questions
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