RecruitingPhase 2NCT06265584

Trial of 2 Step ATG for Prevention of Acute GVHD Post Allogeneic Stem Cell Transplant

Phase II Clinical Trial of 2 Step ATG Combined With Tacrolimus and Mini Methotrexate for Prevention of Acute GVHD Post Reduced Intensity Allogeneic Stem Cell Transplant


Sponsor

University of Alabama at Birmingham

Enrollment

56 participants

Start Date

Apr 8, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

In an effort to reduce graft versus host disease (GVHD) and enhance graft versus leukemia (GVL) effect post allogenic hematopoietic stem cell transplantation (AHSCT), recent research has focused on host immune cell depletion. Frame shifting anti-thymocyte globulin (ATG) backwards to earlier days before days 0 can result in deeper host and less graft T-cell depletion, leading to better immune reconstitution. Preliminary data where 80% of the ATG dose is given on days -6,-5,-4 and 20% given on day -1, showed effective prevention of severe acute GVHD, chronic GVHD and favorable early immune reconstitution. We hypothesize that our 2 step ATG dosing platform when combined with standard tacrolimus and mini methotrexate can prevent grade III-IV acute GVHD and chronic GVHD, resulting in improvement of GVHD/relapse free survival at one year post transplant.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a two-step dosing approach of a medication called ATG (anti-thymocyte globulin) to see if it can reduce graft-versus-host disease (GVHD) — a complication where transplanted immune cells attack the patient's body — after a bone marrow or stem cell transplant. **You may be eligible if...** - You are between 18 and 75 years old - You have a blood cancer or bone marrow condition requiring a stem cell transplant - You have a well-matched donor (related sibling or unrelated donor matched at specific genes) - You are a candidate for a reduced-intensity (gentler) transplant preparation regimen, often due to age or health history **You may NOT be eligible if...** - You do not have a matched stem cell donor - You are too ill or have significant organ dysfunction making transplant unsafe - You have had prior stem cell transplants Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGATG dosing platform when combined with standard tacrolimus and mini methotrexate

On Day -8, you will be admitted to the hospital and receive a dose of prednisone at 1 mg/kg (ATG premedication). You will receive a steroids 3 hours before every ATG infusion. On day -7, you will receive a small dose of ATG as an intravenous (IV) infusion. ATG will be repeated on days -6, -5 and -1. Routine transplant chemotherapy agent fludarabine will be given on days -7 to -3 as daily IV infusions. Melphalan, another routine transplant chemotherapy will be given on day -4 as IV infusion. Tacrolimus (standard immune suppression agent) will start on day -3 as continuous IV infusion and switched to oral after engraftment. Methotrexate is another standard immune suppression medication which is given IV on day +1, +3, +6, and +11 post-transplant. We plan to draw blood on days -4,, -1, +3, +7, and +14 to measure ATG levels.


Locations(1)

University of Alabama at Birmingham

Birmingham, Alabama, United States

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NCT06265584


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