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Completed Not applicable Interventional Results available

Molecular Guided Therapy for Refractory or Recurrent Neuroblastoma

ClinicalTrials.gov ID: NCT01355679

Public ClinicalTrials.gov record NCT01355679. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 10, 2026, 9:42 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Feasibility Trial Using Molecular-Guided Therapy for the Treatment of Patients With Refractory or Recurrent Neuroblastoma

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to test the feasibility (ability to be done) of an experimental test to help plan your cancer treatment. This study plan is not studying the effectiveness of the proposed combinations of therapy for your cancer that you may receive after the experimental testing. This study will look at an experimental technology to determine a tumor's molecular makeup (gene expression profile). This technology (called "OncInsights") is being used to discover new ways to understand cancers and potentially predict the best treatments for patients with cancer in the future. The experimental technology has not been approved by the U.S. Food and Drug Administration.

Study identification

NCT ID
NCT01355679
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Giselle Sholler
Other
Enrollment
16 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range
1 Year and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2011
Primary completion
Aug 31, 2013
Completion
Dec 31, 2014
Last update posted
Aug 5, 2024

2011 – 2015

United States locations

U.S. sites
7
U.S. states
6
U.S. cities
7
Facility City State ZIP Site status
Connecticut Children's Hospital Hartford Connecticut 06106
Arnold Palmer Hospital for Children- MD Anderson Orlando Florida 32806
National Cancer Institute Bethesda Maryland 20877
Helen DeVos Children's Hospital Grand Rapids Michigan 49503
Children's Mercy Hospitals and Clinics Kansas City Missouri 64108
Cardinal Glennon Children's Medical Center St Louis Missouri 63104
Levine Children's Hospital Charlotte North Carolina 28204

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01355679, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 5, 2024 · Synced Sep 10, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01355679 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →