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| ID | Type | Description | Link |
|---|---|---|---|
| MT2017-30 | Other Identifier | University of Minnesota Masonic Cancer Center |
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Study no longer needed
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This is a Phase II study for the use of T-cell replete reduced intensity conditioning (RIC) haploidentical donor allogeneic hematopoietic cell transplantation (HaploHCT) for individuals with high-risk non-malignant diseases who lack a suitable HLA-matched sibling donor.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| rATG, FLU/CY/TBI, & Thiotepa | Experimental | Anti-Thymocyte Globulin - Rabbit (rATG), Fludarabine (Fludara), Cyclophosphamide (Cytoxan, Neosar), Total Body Irradiation (TBI), & Thiotepa |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Blood and Marrow Transplant | Procedure | Reduced intensity conditioning (RIC) with rabbit ATG, fludarabine, cyclophosphamide, thiotepa and low dose (2 Gy) total body irradiation followed by T-cell replete, unmanipulated, haploidentical related donor stem cell transplant (HaploHCT) and post-transplant cyclophosphamide (PTCy) |
| Measure | Description | Time Frame |
|---|---|---|
| Neutrophil Recovery | Incidence of neutrophil recovery by day +42 | Day 42 |
| Measure | Description | Time Frame |
|---|---|---|
| Overall Survival (OS) | Incidence of overall survival at 1 year | 1 year |
| Primary Graft Failure (neutropenic and non-neutropenic) | Incidence of primary graft failure (neutropenic and non-neutropenic) by day +42 |
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Inclusion Criteria:
Sickle Cell Disease (SCD)
* If diagnosis of SCD must meet one or more of the following disease characteristics:
Transfusion Dependent Alpha- or Beta-Thalassemia
Other Non-Malignant Hematologic Disorders:
Transfusion dependent or involve other potential life-threatening cytopenias, including but not limited to Paroxysmal Nocturnal Hemoglobinuria, Glanzmann's Thrombasthenia, Severe Congenital Neutropenia and Shwachman-Diamond Syndrome
cALD
Other inherited metabolic disorders:
Any other inherited metabolic disorder for which alloHCT is indicated and for whom, in the opinion of the treating physician, the patient's best treatment option is with a haploidentical donor following non-myeloablatve conditioning.
Age, Performance Status, Consent
Adequate Organ Function
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Christen L Ebens, MD, MPH | University of Minnesota - Pediatrics Blood and Marrow Transplant | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Masonic Caner Center at University of Minnesota | Minneapolis | Minnesota | 55455 | United States |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Jan 15, 2020 |
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|
| Day 42 |
| Jun 25, 2024 |
| Prot_SAP_000.pdf |
| ICF | No | No | Yes | Informed Consent Form | Oct 21, 2022 | Jun 25, 2024 | ICF_001.pdf |
| ID | Term |
|---|---|
| D000755 | Anemia, Sickle Cell |
| D013789 | Thalassemia |
| ID | Term |
|---|---|
| D000745 | Anemia, Hemolytic, Congenital |
| D000743 | Anemia, Hemolytic |
| D000740 | Anemia |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D006453 | Hemoglobinopathies |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
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| ID | Term |
|---|---|
| D001800 | Blood Specimen Collection |
| ID | Term |
|---|---|
| D013048 | Specimen Handling |
| D019411 | Clinical Laboratory Techniques |
| D019937 | Diagnostic Techniques and Procedures |
| D003933 | Diagnosis |
| D011677 | Punctures |
| D013514 | Surgical Procedures, Operative |
| D008919 | Investigative Techniques |
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