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Clinical Trial Summary

Alemtuzumab is an antibody that reduces the strength of the immune system that is given in preparation for allogeneic hematopoietic cell transplant (HCT). In this research study the investigators want to find out if they can adjust the dose of alemtuzumab used as part of allogeneic HCT to target the level of Day 0 (the planned day of graft infusion) to an optimal therapeutic window of 0.15-0.9 ug/mL.


Clinical Trial Description

Alemtuzumab levels at Day 0 can affect: - the chances of developing acute graft versus host disease (GVHD), which is an immune reaction of the donor cells against your own tissues - the chances of developing mixed chimerism, which is having a mixture of your own cells and donor cells after HCT, and - recovery of your immune system following transplant. High levels of alemtuzumab are associated with more mixed chimerism and slower immune recovery, while low levels are associated with more acute GVHD. The investigators have developed a plan to adjust the alemtuzumab dose for patients to target Day 0 levels to fall within an ideal effective range of 0.15-0.9 ug/mL. This range may minimize the risks of these complications. The investigators are conducting this study to determine if the current plan for alemtuzumab dosing will be successful in the majority of patients and evaluate the impact on the clinical outcomes of acute GVHD, mixed chimerism, and immune recovery. ;


Study Design


Related Conditions & MeSH terms

  • Allogeneic Hematopoietic Cell Transplantation

NCT number NCT05501756
Study type Interventional
Source Children's Hospital Medical Center, Cincinnati
Contact Caitlin Cottrell
Phone 513-803-7039
Email Caitlin.Cottrell@cchmc.org
Status Recruiting
Phase Phase 2
Start date January 11, 2023
Completion date August 31, 2028

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