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Clinical Trials/NCT01850108
NCT01850108
Active, not recruiting
Not Applicable

A Non-Myeloablative Conditioning and Transplantation of Partially HLA-Mismatched and HLA-Matched Bone Marrow for Patients With Sickle Cell Disease and Other Hemoglobinopathies

Vanderbilt-Ingram Cancer Center3 sites in 3 countries26 target enrollmentMay 2013

Overview

Phase
Not Applicable
Intervention
Thymoglobulin
Conditions
Sickle Cell Disease
Sponsor
Vanderbilt-Ingram Cancer Center
Enrollment
26
Locations
3
Primary Endpoint
Transplant-related Mortality (TRM)
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

Allogeneic blood or marrow transplantation (alloBMT) is a curative therapy for a variety of hematologic disorders, including sickle cell disease and thalassemia. Even when it is clear that alloBMT can give to these patients an improvement in their disease, myeloablative transplants have important toxicities and mortalities associated. The lack of suitable donors continues to be a limit to access to transplantation. Substantial progress has been made recently in the development of pre-treatment regimens that facilitate the sustained engraftment of donor marrow with reduced toxicity. Most of these regimens incorporate highly immunosuppressive drugs, which allow the reduction or elimination of myeloablative agents or total body irradiation without endangering the sustained engraftment of HLA-identical allogeneic stem cells. Preliminary results of non-myeloablative allogeneic stem cell transplantation suggest that the procedure can be performed in patients who are ineligible for myeloablative alloBMT, and that sustained remissions of several hematologic malignancies can be obtained.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
December 31, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Adetola A. Kassim

Professor of Medicine; Clinical Director, Sickle Cell Anemia Program; Medical Oncologist

Vanderbilt-Ingram Cancer Center

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Non-Myeloablative Conditioning and Bone Marrow Transplantation

Intervention: Thymoglobulin

Non-Myeloablative Conditioning and Bone Marrow Transplantation

Intervention: Fludarabine

Non-Myeloablative Conditioning and Bone Marrow Transplantation

Intervention: Cyclophosphamide (CTX)

Non-Myeloablative Conditioning and Bone Marrow Transplantation

Intervention: Mesna

Non-Myeloablative Conditioning and Bone Marrow Transplantation

Intervention: Sirolimus

Non-Myeloablative Conditioning and Bone Marrow Transplantation

Intervention: Mycophenolate mofetil (MMF)

Non-Myeloablative Conditioning and Bone Marrow Transplantation

Intervention: Bone marrow transplantation

Non-Myeloablative Conditioning and Bone Marrow Transplantation

Intervention: Total body irradiation

Outcomes

Primary Outcomes

Transplant-related Mortality (TRM)

Time Frame: at 1 year after BMT

Defined as death in the absence of recurrent sickle cell disease or hemoglobinopathy

Secondary Outcomes

  • Number of Patients Who Developed Grade I-IV Acute Graft-vs.-Host Disease(2 years)
  • Number of Patients With Donor Hematopoietic Chimerism in Peripheral Blood <95% at 6 Months After Mini-haploBMT(Up to approximately 180 after mini-haploBMT)
  • Number of Participants With Hematologic and Non-hematologic Toxicities Following minihaploBMT(Day 60 after BMT)

Study Sites (3)

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