Actively Recruiting
MT2025-35 Allogeneic Hematopoietic Stem Cell Transplantation Using Reduced Intensity Conditioning Treosulfan and Fludarabine, With Post-Transplant Cytoxan (PTCy) for the Treatment of Hematological Diseases
Led by Masonic Cancer Center, University of Minnesota · Updated on 2026-04-16
132
Participants Needed
1
Research Sites
463 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This is a Phase II study following subjects proceeding with Treosulfan (36g/m2) preparative regimen followed by a related, unrelated, or partially matched family donor stem cell infusion, with post-transplant cyclophosphamide (PTCy) at 40mg/kg, tacrolimus and MMF for GVHD prophylaxis.
CONDITIONS
Official Title
MT2025-35 Allogeneic Hematopoietic Stem Cell Transplantation Using Reduced Intensity Conditioning Treosulfan and Fludarabine, With Post-Transplant Cytoxan (PTCy) for the Treatment of Hematological Diseases
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 2 to 75 years
- Karnofsky score 70% or higher if 5 years or older; Lansky play score 50 or higher if under 16 years
- Donor match: 5/6 or 6/6 related donor, 5-8/8 HLA matched unrelated donor, or haplotype matched related donor
- Adequate liver function (no decompensated liver failure, Child-Pugh A, AST/ALT less than 5 times upper limit)
- Adequate kidney function (creatinine less than 2.0)
- No decompensated congestive heart failure or uncontrolled arrhythmia
- Left ventricular ejection fraction 40% or higher
- Lung function (DLCO, FEV1, FVC) 40% or higher predicted and no oxygen requirement
You will not qualify if you...
- Pregnant or breastfeeding
- Untreated or uncontrolled HIV infection
- Untreated active serious infection
- Active central nervous system malignancy
- Chronic myeloid leukemia in blast crisis not in complete remission
- Less than 3 months since prior myeloablative transplant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Masonic Cancer Center at University of Minnesota
Minneapolis, Minnesota, United States, 55455
Actively Recruiting
Research Team
C
Christopher Graham, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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