Neuroblastoma Biology Study

N2004-05: Neuroblastoma Biology Study

Medical scientists want to find better ways to treat neuroblastoma and to find ways to prevent the tumor from growing back. To do this, they need more information about the characteristics of neuroblastoma cells. Therefore, they want to study samples of neuroblastoma tissues and neuroblastoma and normal cells in the blood and bone marrow that may be related to the growth of neuroblastoma cells. Doctors and other medical scientists also want to find better ways to detect and measure neuroblastoma to improve the ability to follow the response of tumor cells to therapy.

Study Overview

Status

Recruiting

Conditions

Detailed Description

The purposes of this study are:

To establish a storage place or bank of samples of blood, bone marrow, and/or tumor, and molecular components isolated from these samples from children with neuroblastoma. The stored specimens will be shared with laboratory researchers studying high risk neuroblastoma.

To collect clinical data (such as treatments received, date of diagnosis, tumor stage, etc) and radiology scans to provide this information as needed for the laboratory studies to be done on the specimens.

To obtain neuroblastoma tumor cells from tumor tissue, bone marrow, and/or blood to use to start cell lines, or tumor cells that will keep growing in the laboratory. These cell lines will be shared with laboratory researchers studying high risk neuroblastoma.

Study Type

Observational

Enrollment (Estimated)

1000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Ontario
      • Toronto, Ontario, Canada, M5G 1X8
        • Recruiting
        • Hospital for Sick Children
        • Contact:
          • Daniel Morgenstern, MD
    • California
      • Los Angeles, California, United States, 90027-0700
        • Recruiting
        • Children's Hospital Los Angeles
        • Contact:
          • Araz Marachelian, MD
      • Palo Alto, California, United States, 94305
        • Completed
        • Lucille Salter Packer Children's Hospital, Stanford University
      • San Francisco, California, United States, 94115
        • Recruiting
        • UCSF Helen Diller Family Comprehensive Cancer Center
        • Contact:
          • Kieuhoa Vo, MD
    • Colorado
      • Aurora, Colorado, United States, 80045
        • Recruiting
        • Children Hospital of Colorado
        • Contact:
          • Margaret Macy, MD
    • Georgia
      • Atlanta, Georgia, United States, 30322
        • Recruiting
        • AFLAC Cancer Center and Blood Disorders Service of Children's Healthcare of Atlanta - Egleston Campus
        • Contact:
          • Kelly Goldsmith, MD
    • Illinois
      • Chicago, Illinois, United States, 60637
        • Recruiting
        • University of Chicago, Comer Children's Hospital
        • Contact:
          • Ami Desai, MD
    • Massachusetts
      • Boston, Massachusetts, United States, 02115
        • Recruiting
        • Children's Hospital Boston
        • Contact:
          • Suzanne Shusterman, MD
    • Michigan
      • Ann Arbor, Michigan, United States, 48109
        • Recruiting
        • C.S Mott Children's Hospital
        • Contact:
          • Rajen Mody, MD
    • North Carolina
      • Chapel Hill, North Carolina, United States, 27599
        • Completed
        • University of North Carolina
    • Ohio
      • Cincinnati, Ohio, United States, 45229-3039
        • Recruiting
        • Cincinnati Children's Hospital Medical Center
        • Contact:
          • Katherine Somers, MD
      • Columbus, Ohio, United States, 43205
        • Recruiting
        • Nationwide Children's Hospital
        • Contact:
          • Keri Streby, MD
    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19104-4318
        • Recruiting
        • Children's Hospital of Philadelphia
        • Contact:
          • Yael Mosse, MD
    • Tennessee
      • Memphis, Tennessee, United States, 38105
        • Not yet recruiting
        • St. Jude Children's Research Hospital
        • Contact:
          • Sara Federico, MD
    • Texas
      • Dallas, Texas, United States, 75235
        • Not yet recruiting
        • University of Texas Southwestern
        • Contact:
          • Tanya Watt, MD
      • Fort Worth, Texas, United States, 76104
        • Recruiting
        • Cook Children's Medical Center - Fort Worth
        • Contact:
          • Chelsee Greer, DO
    • Washington
      • Seattle, Washington, United States, 98105
        • Recruiting
        • Seattle Children's Hospital
        • Contact:
          • Mark Fluchel, MD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

1 month to 99 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Neuroblastoma patients from various NANT sites.

Description

Inclusion Criteria:

  • Patients must be greater than or 31 days of age.
  • Patients must have had a diagnosis of high risk neuroblastoma either by histological verification of neuroblastoma and/or demonstration of tumor cells in the bone marrow with increased urinary catecholamines.
  • All patients with refractory or recurrent high risk neuroblastoma at NANT institutions are eligible regardless of disease status (including no measurable or evaluable tumor) as long as they undergo a disease evaluation and appropriate samples are submitted.
  • Additionally, all patients with high risk neuroblastoma without relapse treated at a NANT institution are eligible if undergoing a disease evaluation, as long as Children's Oncology Group specimens are prioritized.

Exclusion Criteria:

  • There are no exclusion criteria on this study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Shahab Asgharzadeh, MD, Children's Hospital Los Angeles

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2011

Primary Completion (Estimated)

December 1, 2099

Study Completion (Estimated)

December 1, 2099

Study Registration Dates

First Submitted

April 26, 2012

First Submitted That Met QC Criteria

April 27, 2012

First Posted (Estimated)

April 30, 2012

Study Record Updates

Last Update Posted (Actual)

March 23, 2026

Last Update Submitted That Met QC Criteria

March 19, 2026

Last Verified

March 1, 2026

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Neuroblastoma

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