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Completed Phase 1 Interventional

N2007-03: Vorinostat and 131-I MIBG in Treating Patients With Resistant or Relapsed Neuroblastoma

ClinicalTrials.gov ID: NCT01019850

Public ClinicalTrials.gov record NCT01019850. 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 Oct 20, 2026, 11:52 AM EDT

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

Official title

Vorinostat With 131-I MIBG Therapy for Resistant/Relapsed Neuroblastoma: A Phase I Study IND# 105,744

Brief summary

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

RATIONALE: Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Radioactive drugs, such as iobenguane I 131, may carry radiation directly to tumor cells and not harm normal cells. Giving vorinostat together with iobenguane I 131 may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of giving vorinostat together with iobenguane I 131 in treating patients with resistant or relapsed neuroblastoma.

Study identification

NCT ID
NCT01019850
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
27 participants

Conditions and interventions

Conditions

Interventions

Drug · Radiation · Procedure

Eligibility (public fields only)

Age range
2 Years to 30 Years
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
Mar 2010 (Type not available)
Primary completion
Dec 2014 (Actual)
Completion
Feb 2015 (Actual)
Last update posted
Apr 10, 2023

2010 – 2015

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Children's Hospital Los Angeles Los Angeles California 90027 —
Lucile Salter Packer Children's Hospital Palo Alto California 94304 —
UCSF Helen Diller Family Comprehensive Cancer Center San Francisco California 94143 —
AFLAC Cancer Center and Blood Disorders Service of Children's Healthcare of Atlanta - Egleston Campus Atlanta Georgia 30322 —
University of Chicago, Comer Children's Hospital Chicago Illinois 60637 —
Children's Hospital Boston Boston Massachusetts 02115 —
C.S Mott Children's Hospital Ann Arbor Michigan 48109 —
Duke University Medical Center Durham North Carolina 27710 —
Cincinnati Children's Hospital Medical Center Cincinnati Ohio 45229-3039 —
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104-4318 —
Cook Children's Medical Center - Fort Worth Fort Worth Texas 76104 —
Children's Hospital and Regional Medical Center - Seattle Seattle Washington 98105 —

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 NCT01019850, 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 Apr 10, 2023 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01019850 live on ClinicalTrials.gov.

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