Actively Recruiting
Optimized Cord Blood Transplantation for the Treatment of Patients With High-risk Hematologic Malignancies Who Have Relapsed After First Allogeneic Stem Cell Transplantation
Led by M.D. Anderson Cancer Center · Updated on 2026-04-28
35
Participants Needed
1
Research Sites
247 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical research study is to learn if intermediate-intensity conditioning therapy followed by a cord blood transplant can help to control high-risk hematological malignancies in patients who need a second allogeneic stem cell transplantation.
CONDITIONS
Official Title
Optimized Cord Blood Transplantation for the Treatment of Patients With High-risk Hematologic Malignancies Who Have Relapsed After First Allogeneic Stem Cell Transplantation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient aged 0 to 60 years at time of consent
- Relapse more than 100 days after first stem cell transplant
- Diagnosis of acute myelogenous leukemia, acute lymphoblastic leukemia, other acute leukemias, myelodysplastic syndromes, or CMML without myelofibrosis
- Must have received one prior allogeneic stem cell transplantation
- Karnofsky score 70% or higher if age 16 or older, or Lansky score 70% or higher if under 16
- Kidney function with creatinine clearance over 50 ml/min
- Bilirubin less than 2 mg/dL unless benign causes
- ALT less than 5 times upper limit of normal
- Pulmonary function with DLCO 60% or more predicted, or waived if unable to complete test
- Left ventricular ejection fraction over 50%
- Two cord blood units meeting specific HLA match and cell dose criteria, including minimum 3/8 HLA match, cell doses, and cryopreservation standards
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
The University of Texas M. D. Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
Research Team
W
Warren Fingrut, 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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