Clinical trial

Reduced Intensity Conditioning (RIC) Regimen for Patients With Non-malignant Disorders

Name
08-005658
Description
This is a Phase II pilot study to evaluate engraftment and toxicity of patients with non-malignant diseases using a reduced intensity conditioning regimen in the setting of allogeneic transplant for non malignant diseases. Bone Marrow or cord blood will be acceptable as a stem cell source. Recently, reduced intensity conditioning (RIC) regimens have been used for both adult patients with leukemias and pediatric patients with non-malignant diseases. These regimens are better tolerated, resulting in less transplant related morbidity and mortality. Stable mixed chimerism, while insufficient for eradication of leukemias, may be sufficient to cure patients with non-malignant diseases.
Trial arms
Trial start
2008-01-01
Estimated PCD
2025-12-01
Trial end
2026-12-01
Status
Active (not recruiting)
Phase
Early phase I
Treatment
RIC: Distal Campath
Campath, Fludarabine, Melphalan, Cyclosporine, Cellcept (MMF)
Arms:
RIC: Distal Campath
Other names:
Reduced Intensity Conditioning Regimen
RIC:Intermediate Campath
Campath, Fludarabine, Melphalan, Cyclosporine, Cellcept (MMF)
Arms:
RIC:Intermediate Campath
Other names:
Reduced Intensity Conditioning Regimen
RIC: Mini Busulfan
Campath, Fludarabine, Busulfan, Cyclosporine, Cellcept (MMF)
Arms:
RIC: Mini Busulfan
Other names:
Reduced Intensity Conditioning Regimen
Size
75
Primary endpoint
Engraftment
Post Transplant -100 days
Eligibility criteria
Inclusion Criteria: 1. Age \>6 months- 25 years 2. Diseases eligible for Distal Alemtuzumab: * Immunodysregulation polyendocrinopathy enteropathy X-linked (IPEX) syndrome * Sickle cell disease * Thalassemia major * Bone marrow failure 3. Diseases eligible for Intermediate Alemtuzumab * Hemophagocytic lymphohistiocytosis other macrophage activation syndromes, severe Langerhans histiocytosis * Severe combined immune deficiency, adenosine deaminase deficiency, common variable immunodeficiency * Wiskott-Aldrich syndrome 4. Organ criteria: * Cardiac: Echocardiogram shortening fraction \>27% * Renal: Serum creatinine less than 1.5 times the upper limit of normal for age * Hepatic: liver function tests must be less than 5 times the upper limit of normal 5. No active infections Exclusion criteria 1. Uncontrolled bacterial, fungal or viral infections
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NON_RANDOMIZED', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 75, 'type': 'ESTIMATED'}}
Updated at
2024-02-28

1 organization

3 products

3 indications