Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Acute Leukemia
  • Aplastic Anemia
  • Chronic Leukemia
  • Congenital Hematological Disorder
  • Immune Deficiency Disorder
  • Lymphoma
  • Metabolism Disorder
  • Multiple Myeloma
  • Myelodysplastic Syndromes
  • Solid Tumor
Type
Interventional
Phase
Phase 1
Design
Allocation: Non-RandomizedIntervention Model: Parallel AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Younger than 275 years
Gender
Both males and females

Description

This study is a single-center treatment protocol with four possible preparative regimens, designed to validate the process of umbilical cord blood stem cell transplantation at our institution. Enrolled patients will receive chemotherapy +/-total body radiation as a pre-transplant conditioning regime...

This study is a single-center treatment protocol with four possible preparative regimens, designed to validate the process of umbilical cord blood stem cell transplantation at our institution. Enrolled patients will receive chemotherapy +/-total body radiation as a pre-transplant conditioning regimen. Patients will then receive cord blood stem cells followed by GvHD prophylaxis that will include Tacrolimus and Mycophenolate Mofetil, or Cyclosporin A and Methylprednisolone. Multiple data points will be collected prior to, during, and following transplantation to ensure safety of the process and to evaluate the stated objectives.

Tracking Information

NCT #
NCT03016806
Collaborators
Not Provided
Investigators
Principal Investigator: Jane L Liesveld, MD Medical Director, Blood & Marrow Transplant Unit