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Completed Phase 1 Interventional

URMC Related Haplo-identical Donor BMT

ClinicalTrials.gov ID: NCT02660281

Public ClinicalTrials.gov record NCT02660281. 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 8, 2026, 5:00 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

Haploidentical Donor Hematopoietic Stem Cell Transplantation

Study identification

NCT ID
NCT02660281
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
University of Rochester
Other
Enrollment
74 participants

Conditions and interventions

Interventions

  • Busulfan Drug
  • Fludarabine Drug
  • Melphalan Drug
  • Post-Stem Cell Infusion Cyclophosphamide Drug
  • Post-Stem Cell Infusion Mesna Drug
  • Pre-Stem Cell Infusion Cyclophosphamide Drug
  • Pre-Stem Cell Infusion Mesna Drug
  • Stem Cell Infusion Procedure
  • Thiotepa Drug
  • Total Body Irradiation 1200 cGy Radiation

Drug · Procedure · Radiation

Eligibility (public fields only)

Age range
6 Months to 75 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
Sep 30, 2015
Primary completion
Oct 27, 2019
Completion
Jan 6, 2021
Last update posted
Nov 2, 2021

2015 – 2021

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Wilmot Cancer Institute Rochester New York 14642

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 NCT02660281, 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 Nov 2, 2021 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02660281 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →