Bone Marrow Transplant Clinical Trials

Clinical trials related to Bone Marrow Transplant Procedure

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

Status: Recruiting
Location: See location...
Intervention Type: Biological, Drug, Radiation
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 75
Healthy Volunteers: f
View:

• Patients 2-75 years of age

• ≤7 5 years of age: Karnofsky score ≥ 70% (≥ 16 years) or Lansky play score ≥ 50 (\< 16 years) with appropriate organ criteria as below (in other inclusion criteria)

• 5/6 or 6/6 related donor, OR a 5-8/8 HLA-A, B, C, DRB1 allele match unrelated donor, OR a haplotype (at least 5/10) related donor

• adequate liver (no decompensated liver failure, Child Pugh A, AST/ALT \<5X ULN) and renal function (creatinine \<2.0)

• absence of decompensated congestive heart failure, or uncontrolled arrhythmia and left ventricular ejection fraction ≥ 40%

• DLCO FEV1, FVC ≥ 40% predicted, and absence of O2 requirement

Locations
United States
Minnesota
Masonic Cancer Center at University of Minnesota
RECRUITING
Minneapolis
Contact Information
Primary
Christopher Graham, MD
grah0329@umn.edu
612-625-3051
Time Frame
Start Date: 2026-04-10
Estimated Completion Date: 2035-03
Participants
Target number of participants: 132
Treatments
Experimental: Treo/Flu with PTCy
Subjects treated with Treosulfan and Fludarabine preparative regimen with TBI for AML and MDS patients followed by a related or unrelated donor stem cell infusion utilizing PTCy, tacrolimus and MMF as GVHD prophylaxis.
Sponsors
Leads: Masonic Cancer Center, University of Minnesota

This content was sourced from clinicaltrials.gov

Similar Clinical Trials