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To investigate the safety of partially matched related human placental-derived stem cells (HPDSC) administered in conjunction with umbilical cord blood (UCB) stem cells from the same donor in subjects with various malignant or nonmalignant disorders potentially curable with stem cell transplantation and to assess potential restoration of normal hematopoiesis and immune function in subjects with these disorders
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | all subjects will be treated with UCB and HPDSC |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| UCB and HPDSC | Procedure | single dose of UCB followed by one unit of HPDSC |
|
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of GVHD, time to engraftment and survival | 2 years |
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Inclusion Criteria:
Exclusion Criteria:
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subjects requiring cord blood transplantation
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| Name | Affiliation | Role |
|---|---|---|
| Lolie Yu, MD | Louisiana State University Children's Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Louisiana State University Children's Hospital | New Orleans | Louisiana | 70118 | United States |
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| ID | Term |
|---|---|
| D019337 | Hematologic Neoplasms |
| D009190 | Myelodysplastic Syndromes |
| D015470 | Leukemia, Myeloid, Acute |
| D054198 | Precursor Cell Lymphoblastic Leukemia-Lymphoma |
| D000755 | Anemia, Sickle Cell |
| D017086 | beta-Thalassemia |
| D008661 | Metabolism, Inborn Errors |
| D053632 | X-Linked Combined Immunodeficiency Diseases |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D001855 | Bone Marrow Diseases |
| D007951 | Leukemia, Myeloid |
| D007938 | Leukemia |
| D009370 | Neoplasms by Histologic Type |
| D007945 | Leukemia, Lymphoid |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
| D000745 | Anemia, Hemolytic, Congenital |
| D000743 | Anemia, Hemolytic |
| D000740 | Anemia |
| D006453 | Hemoglobinopathies |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D013789 | Thalassemia |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D040181 | Genetic Diseases, X-Linked |
| D016511 | Severe Combined Immunodeficiency |
| D000081207 | Primary Immunodeficiency Diseases |
| D007232 | Infant, Newborn, Diseases |
| D007153 | Immunologic Deficiency Syndromes |
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