A Study of Hematopoietic Stem Cell Transplantation (HSCT) in Non-Malignant Disease Using a Reduced-Intensity Preparatory Regime

Who is this study for? Patients with non-malignant diseases
What treatments are being studied? Hematopoietic Stem Cell Transplantation using a reduced-intensity preparatory regime
Status: Recruiting
Location: See all (18) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1/Phase 2
SUMMARY

The hypothesis for this study is that a preparative regimen that maximizes host immunosuppression without myeloablation will be well tolerated and sufficient for engraftment of donor hematopoietic cells. It is also to determine major toxicities from these conditioning regimens, within the first 100 days after transplantation.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 20
Healthy Volunteers: f
View:

⁃ Stratum 1: Patient must have non-malignant disorder, excluding thalassemia. Must be receiving a 8/8 HLA-matched bone marrow, related or unrelated Stratum 2: Patient must have thalassemia receiving 8/8 HLA-matched bone marrow or 5-8/8 HLA-matched UCB. Related or unrelated.

⁃ Stratum 3: Patient must have a hemoglobinopathy receiving 7/8 HLA-matched bone marrow or 5-8/8 HLA-matched UCB. Related or unrelated.

⁃ Stratum 4: Patient must have a non-malignant disorder (excluding hemoglobinopathy) receiving 7/8 HLA-matched bone marrow or 5-8/8 HLA-matched UCB. Related or unrelated.

⁃ All strata:

• Recipient age \< 21 years

• Lansky/Karnofsky \>/= 40

• Adequate pulmonary, renal, liver, and other organ function as defined in protocol

• Negative pregnancy test

• Adequate total nucleated cell or CD34+ dose of product as defined in protocol

• If sickle cell, Hemoglobin S \<30%

Locations
United States
Arizona
Phoenix Children's Hospital
RECRUITING
Phoenix
California
Children's Hospital of Orange County
RECRUITING
Orange
University of California
RECRUITING
San Diego
Connecticut
Yale School of Medicine
RECRUITING
New Haven
Washington, D.c.
George Washington University School of Medicine
RECRUITING
Washington D.c.
Florida
Miami Children's Hospital
RECRUITING
Miami
University of Miami
RECRUITING
Miami
All Children's Hospital
RECRUITING
St. Petersburg
Illinois
Children's Memorial Hospital
COMPLETED
Chicago
Indiana
Indiana University School of Medicine
RECRUITING
Indianapolis
Missouri
St. Louis University
RECRUITING
St Louis
Washington University School of Medicine (in St. Louis)
RECRUITING
St Louis
North Carolina
Carolinas Medical Center
RECRUITING
Charlotte
New Jersey
Hackensack University Medical Center
COMPLETED
Hackensack
New York
Columbia University Medical Center
RECRUITING
New York
Oklahoma
The University of Oklahoma
COMPLETED
Oklahoma City
Texas
Texas Transplant Institute
RECRUITING
San Antonio
Other Locations
Canada
University of Calgary
RECRUITING
Calgary
Contact Information
Primary
Stephanie Hyde, CCRP
stephanie.day@wustl.edu
3142861180
Time Frame
Start Date: 2001-12
Estimated Completion Date: 2031-12
Participants
Target number of participants: 220
Treatments
Experimental: Stratum 1
Recipients with non-malignant disorders, excluding thalassemia. Related or unrelated 8/8 HLA-matched bone marrow
Experimental: Stratum 2
Recipient with transfusion dependent thalassemia. Related or unrelated. 8/8 HLA-matched bone marrow or 5-8/8 HLA-matched UCB
Experimental: Stratum 3
Recipient with hemoglobinopathy Related or unrelated. 7/8 HLA-matched bone marrow or 5-8/8 HLA-matched UCB
Experimental: Stratum 4
Recipient with non-malignant disorder, excluding hemoglobinopathy Related or unrelated. 7/8 HLA-matched bone marrow or 5-8/8 HLA-matched UCB
Sponsors
Leads: Washington University School of Medicine
Collaborators: St. Louis Children's Hospital

This content was sourced from clinicaltrials.gov