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RecruitingNeuroblastoma

Pediatric Precision Laboratory Advanced Neuroblastoma Therapy

Eligible age

Up to 22 yrs

Accepts

All genders

Locations

19 states

Healthy volunteers

No

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About this study

A prospective open label, multicenter study to evaluate the feasibility and acute toxicity of using molecularly guided therapy in combination with standard therapy followed by a Randomized Controlled Trial of standard immunotherapy with or without DFMO followed by DFMO maintenance for Subjects with Newly Diagnosed High-Risk Neuroblastoma.

Sponsor: Giselle Sholler

You may not qualify if…

  • 1. Subjects who are 12-18 months of age with INSS Stage 4 and all stage 3 subjects with favorable biologic features (ie, nonamplified MYCN, favorable pathology, and DNA index \> 1) are not eligible.
  • 2. Lactating females are not eligible unless they have agreed not to breastfeed their infants.
  • 3. Subjects receiving any investigational drug concurrently.
  • 4. Subjects with any other medical condition, including but not limited to malabsorption syndromes, mental illness or substance abuse, deemed by the Investigator to be likely to interfere with the interpretation of the results or which would interfere with a subject's ability to sign or the legal guardian's ability to sign the informed consent, and subject's ability to cooperate and participate in the study

Where it's recruiting

Alabama

Birmingham

Arkansas

Little Rock

California

Oakland · San Diego

Connecticut

Hartford

Florida

Miami · Orlando · Tampa

Georgia

Augusta

Hawaii

Honolulu

Idaho

Boise

Illinois

Chicago

Kentucky

Louisville

Michigan

Grand Rapids

Minnesota

Minneapolis

Source: ClinicalTrials.gov · NCT02559778 · last updated 2026-04-28

Pediatric Precision Laboratory Advanced Neuroblastoma Therapy · TrialPath