A Multicenter Access and Distribution Protocol for Unlicensed Cryopreserved Cord Blood Units (CBUs) for Transplantation in Pediatric and Adult Patients with Hematologic Malignancies and Other Indications
- Sponsor:
- National Marrow Donor Program - NMDP
- Sponsor Study ID:
- 10-CBA
- CTO #:
- 101593
- NCT Number:
- NCT01351545
- Phase:
- N/A
- Protocol Type:
- Other
- Age Group:
- Adults
- Disease Sites:
- Hodgkin's Lymphoma; Leukemia, other; Lymphoid Leukemia; Multiple Myeloma; Myeloid and Monocytic Leukemia; Non-Hodgkin's Lymphoma; Other Hematopoietic
- Study Objectives:
- The primary aim of this study is to examine the incidence of neutrophil recovery of 500/mm3 after cord blood transplantation in a multi-institution setting using CBUs that are not Food and Drug Administration (FDA) licensed.
- eConsent:
- Not available
- Study Documents:
-
Open Study Documents
(MUSC NetID required for document access)
For more information about this trial please contact the study team:
-
Medical University of South Carolina
- Principal Investigator, Hudspeth, Michelle, at hudspeth@musc.edu
- Study Coordinator, Pound, Ashton, at pound@musc.edu
Trial opened at the following institutions:
Medical University of South Carolina