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Completed Phase 1 Interventional

Study To Examine Toxicity Of Allogeneic Stem Cell Transplantation For Relapsed Or Therapy Refractory Ewings Sarcoma

ClinicalTrials.gov ID: NCT02472392

Public ClinicalTrials.gov record NCT02472392. 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 May 12, 2026, 2:02 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 Phase I Study to Examine the Toxicity of Allogeneneic Stem Cell Transplantation for Relapsed or Therapy Refractory Ewings

Study identification

NCT ID
NCT02472392
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
University of Louisville
Other
Enrollment
10 participants

Conditions and interventions

Conditions

Interventions

  • Busulfan Drug
  • Cyclophosphamide Drug
  • Fludarabine Drug
  • Melphalan Drug
  • Rabbit anti-thymocyte globulin Drug

Drug

Eligibility (public fields only)

Age range
Up 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 31, 2013
Primary completion
Nov 30, 2016
Completion
Nov 30, 2016
Last update posted
May 8, 2017

2013 – 2016

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
University of Louisville Louisville Kentucky 40202

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 NCT02472392, 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 May 8, 2017 · Synced May 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02472392 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →