- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01587300
Neuroblastoma Biology Study
N2004-05: Neuroblastoma Biology Study
Study Overview
Status
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
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Araz Marachelian, MD
- Phone Number: 323-361-5687
- Email: amarachelian@chla.usc.edu
Study Locations
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Ontario
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Toronto, Ontario, Canada, M5G 1X8
- Recruiting
- Hospital for Sick Children
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Contact:
- Daniel Morgenstern, MD
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California
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Los Angeles, California, United States, 90027-0700
- Recruiting
- Children's Hospital Los Angeles
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Contact:
- Araz Marachelian, MD
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Palo Alto, California, United States, 94305
- Completed
- Lucille Salter Packer Children's Hospital, Stanford University
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San Francisco, California, United States, 94115
- Recruiting
- UCSF Helen Diller Family Comprehensive Cancer Center
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Contact:
- Kieuhoa Vo, MD
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Colorado
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Aurora, Colorado, United States, 80045
- Recruiting
- Children Hospital of Colorado
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Contact:
- Margaret Macy, MD
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Georgia
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Atlanta, Georgia, United States, 30322
- Recruiting
- AFLAC Cancer Center and Blood Disorders Service of Children's Healthcare of Atlanta - Egleston Campus
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Contact:
- Kelly Goldsmith, MD
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Illinois
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Chicago, Illinois, United States, 60637
- Recruiting
- University of Chicago, Comer Children's Hospital
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Contact:
- Ami Desai, MD
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Massachusetts
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Boston, Massachusetts, United States, 02115
- Recruiting
- Children's Hospital Boston
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Contact:
- Suzanne Shusterman, MD
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Michigan
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Ann Arbor, Michigan, United States, 48109
- Recruiting
- C.S Mott Children's Hospital
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Contact:
- Rajen Mody, MD
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North Carolina
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Chapel Hill, North Carolina, United States, 27599
- Completed
- University of North Carolina
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Ohio
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Cincinnati, Ohio, United States, 45229-3039
- Recruiting
- Cincinnati Children's Hospital Medical Center
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Contact:
- Katherine Somers, MD
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Columbus, Ohio, United States, 43205
- Recruiting
- Nationwide Children's Hospital
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Contact:
- Keri Streby, MD
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Pennsylvania
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Philadelphia, Pennsylvania, United States, 19104-4318
- Recruiting
- Children's Hospital of Philadelphia
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Contact:
- Yael Mosse, MD
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Tennessee
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Memphis, Tennessee, United States, 38105
- Not yet recruiting
- St. Jude Children's Research Hospital
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Contact:
- Sara Federico, MD
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Texas
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Dallas, Texas, United States, 75235
- Not yet recruiting
- University of Texas Southwestern
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Contact:
- Tanya Watt, MD
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Fort Worth, Texas, United States, 76104
- Recruiting
- Cook Children's Medical Center - Fort Worth
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Contact:
- Chelsee Greer, DO
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Washington
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Seattle, Washington, United States, 98105
- Recruiting
- Seattle Children's Hospital
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Contact:
- Mark Fluchel, MD
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
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
How is the study designed?
Design Details
Collaborators and Investigators
Investigators
- Study Chair: Shahab Asgharzadeh, MD, Children's Hospital Los Angeles
Study record dates
Study Major Dates
Study Start
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- N2004-05
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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Children's Oncology GroupNational Cancer Institute (NCI)CompletedStage 4S Neuroblastoma | Ganglioneuroblastoma | Stage 2A Neuroblastoma | Stage 2B Neuroblastoma | Stage 3 Neuroblastoma | Stage 4 Neuroblastoma | Stage 1 Neuroblastoma | Stage 2 NeuroblastomaUnited States, Canada, Australia, New Zealand
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Children's Oncology GroupNational Cancer Institute (NCI)CompletedRecurrent Neuroblastoma | Disseminated Neuroblastoma | Localized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S NeuroblastomaUnited States
-
ProgenaBiomeMicrobiome Research FoundationNo longer availableNeuroblastoma | Neuroblastoma. CNS | Neuroblastoma (NB) | Neuroblastoma Recurrent | Neuroblastoma (Measurable Disease) | Neuroblastoma in Children | Neuroblastoma (NBL)United States
-
Children's Oncology GroupNational Cancer Institute (NCI)CompletedLocalized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S Neuroblastoma | Ganglioneuroblastoma | Stage 4 NeuroblastomaUnited States
-
National Cancer Institute (NCI)CompletedRecurrent Neuroblastoma | Localized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S Neuroblastoma | Stage 4 NeuroblastomaUnited States, Canada, Australia, New Zealand, Puerto Rico
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Children's Oncology GroupNational Cancer Institute (NCI)CompletedRecurrent Neuroblastoma | Localized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S Neuroblastoma | Stage 4 NeuroblastomaUnited States, Canada, Australia, New Zealand, Puerto Rico, Switzerland
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Children's Oncology GroupNational Cancer Institute (NCI)Active, not recruitingRecurrent Neuroblastoma | Stage 4S Neuroblastoma | Stage 2A Neuroblastoma | Stage 2B Neuroblastoma | Stage 3 Neuroblastoma | Stage 4 NeuroblastomaUnited States, Canada, Australia, New Zealand
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Children's Oncology GroupNational Cancer Institute (NCI)Active, not recruitingLocalized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S Neuroblastoma | Ganglioneuroblastoma | Stage 4 NeuroblastomaUnited States, Canada, Saudi Arabia, Puerto Rico, Australia, New Zealand, Switzerland, Netherlands
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Children's Oncology GroupNational Cancer Institute (NCI)CompletedLocalized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4S NeuroblastomaUnited States
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Children's Oncology GroupNational Cancer Institute (NCI)CompletedRecurrent Neuroblastoma | Localized Resectable Neuroblastoma | Localized Unresectable Neuroblastoma | Regional Neuroblastoma | Stage 4 NeuroblastomaUnited States