ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

HLA-Mismatched Unrelated Donor Bone Marrow Transplantation With Post-Transplantation Cyclophosphamide

ClinicalTrials.gov ID: NCT02793544

Public ClinicalTrials.gov record NCT02793544. 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 18, 2026, 9:27 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

A Multi-Center, Phase II Trial of HLA-Mismatched Unrelated Donor Bone Marrow Transplantation With Post-Transplantation Cyclophosphamide for Patients With Hematologic Malignancies

Study identification

NCT ID
NCT02793544
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Center for International Blood and Marrow Transplant Research
Network
Enrollment
80 participants

Conditions and interventions

Interventions

  • Busulfan Drug
  • Cyclophosphamide 14.5 mg/kg/day IV on Days -6, -5 Drug
  • Cyclophosphamide 50mg/kg/day IV on Days -2,-1 Drug
  • Cyclophosphamide 50mg/kg/day IV on Days -5,-4 Drug
  • Fludarabine Drug
  • G-CSF Drug
  • Infusion of non-T-cell depleted bone marrow on Day 0 Procedure
  • Mycophenolate mofetil Drug
  • Post-HCT Cyclophosphamide 50mg/kg IV on Day+3, +4 Drug
  • Post-HCT Mesna Drug
  • Pre-HCT Mesna on Days -2 and -1 Drug
  • Pre-HCT Mesna on Days -5 and -4 Drug
  • Pre-HCT Mesna on Days -6 and -5 Drug
  • Sirolimus Drug
  • Total Body Irradiation (TBI) 200cGy on Day -1 Radiation
  • Total Body Irradiation (TBI) 200cGy twice a day on Days -3, -2, -1 Radiation

Drug · Procedure · Radiation

Eligibility (public fields only)

Age range
15 Years to 70 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
Nov 30, 2016
Primary completion
Feb 29, 2020
Completion
Feb 29, 2020
Last update posted
Aug 5, 2025

2016 – 2020

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
Shands HealthCare & University of Florida Gainesville Florida 32610
University of Miami Miami Florida 33136
H. Lee Moffitt Cancer Center and Research Institute Tampa Florida 33612
University of Maryland Greenebaum Cancer Center Baltimore Maryland 21201
The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland 21287
Karmanos Cancer Institute Detroit Michigan 48201
Memorial Sloan Kettering Cancer Center - Adults New York New York 10065
University of North Carolina Hospitals Chapel Hill North Carolina 27599
Ohio State Medical Center, James Cancer Center Columbus Ohio 43210
Virginia Commonwealth University Massey Cancer Center Bone Marrow Transplant Program Richmond Virginia 23298
Froedtert Memorial Lutheran Hospital Milwaukee Wisconsin 53226

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 NCT02793544, 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, 2025 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02793544 live on ClinicalTrials.gov.

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