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Providing Access to Cord Blood Units for Transplants

This study has been withdrawn prior to enrollment.
Sponsor:
Information provided by (Responsible Party):
National Institutes of Health Clinical Center (CC) ( National Cancer Institute (NCI) )
ClinicalTrials.gov Identifier:
NCT01479582
First received: November 22, 2011
Last updated: June 25, 2014
Last verified: November 2012

November 22, 2011
June 25, 2014
October 2011
November 2012   (final data collection date for primary outcome measure)
The primary aim of this study is to examine the incidence of neutrophil recovery of greater than or equal to 500/mm3 after cord blood transplantation in a multi-institution setting using CBUs that are not Food and Drug Administration (FDA) licen...
Same as current
Complete list of historical versions of study NCT01479582 on ClinicalTrials.gov Archive Site
  • Assess incidence of graft rejection.
  • Assess incidence of transmission of infection.
  • Assess incidence of serious infusion reaction.
  • Determine 1 year survival after cord blood transplantation.
  • Assess cumulative incidence of aGVHD vs cGVHD.
Same as current
Not Provided
Not Provided
 
Providing Access to Cord Blood Units for Transplants
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

Background:

- Cord blood banks have been set up to collect and store umbilical cord blood for transplants. These transplants are used to treat different types of cancer. In October 2011, the Food and Drug Administration (FDA) began considering cord blood as a biological drug. Most of the cord blood units currently available in cord blood banks in the United States and other countries were collected before the FDA set these new standards. The units meet standards set by the National Marrow Donor Program (NMDP), but they were not collected, tested, or stored exactly according to FDA standards. As a result, the new guidelines state that they may only be used for transplant if the transplant is done as part of a study. Researchers have set up a study to provide these cord blood units to recipients and to study the effects of their use.

Objectives:

  • To provide access to cord blood units for recipients whose best choice for a unit meets NMDP but not FDA standards.
  • To study the effects of these cord blood transplants.

Eligibility:

- Individuals who need to have a cord blood transplant to treat certain types of cancer.

Design:

  • Participants will be screened with a physical exam, medical history. They will also have blood tests and imaging studies.
  • Participants will have the cord blood transplant and allow their medical data to be collected by the study researchers.

Study Design:

This study is an access and distribution protocol for unlicensed cryopreserved cord blood units (CBUs) in pediatric and adult patients with hematologic malignancies and other indications.

Primary Objective:

The primary aim of this study is to examine the incidence of neutrophil recovery of (Bullet)500/mm3

after cord blood transplantation in a multi-institution setting using CBUs that are not Food and

Drug Administration (FDA) licensed.

Secondary Objectives:

In patients receiving a non-licensed CBU:

  • Assess incidence of graft rejection
  • Assess incidence of transmission of infection
  • Assess incidence of serious infusion reaction
  • Determine 1 year survival after cord blood transplantation
  • Assess cumulative incidence of acute graft vs. host disease (GVHD) grades II to IV and

grades III to IV

  • Assess cumulative incidence of chronic GVHD
  • Determine platelet engraftment of > 20,000 mcL and > 50,000 mcL
  • Determine CBU-derived engraftment

Eligibility Criteria:

Inclusion Criteria

  • Patients with FDA-specified indications (see Appendix B for further details):
  • Hematological malignancies
  • Certain lysosomal storage and peroxisomal enzyme deficiency disorders
  • Hurler syndrome (MPS I)
  • Krabbe Disease (Globoid Leukodystrophy)
  • X-linked Adrenoleukodystrophy
  • Primary immunodeficiency diseases
  • Bone marrow failure
  • Beta-thalassemia
  • Signed informed consent (and signed assent, if applicable)
  • Pediatric and adult patients of any age

Exclusion Criteria

  • Patients who are receiving only licensed CBUs
  • Cord blood transplant recipients at international transplant centers

Treatment Description:

Treatment, including pre-transplant conditioning and GVHD prophylaxis, will occur per each

transplant center s specifications.

Accrual Objective:

In this access and distribution protocol, U.S. patients undergoing transplant using unlicensed

CBUs will be enrolled and there is no accrual maximum.

Accrual Period:

The accrual period is open ended.

Interventional
Phase 2
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Chronic Myelogous Leukemia/Other Leukemia
  • Acute Leukemias
  • MDS/MPS
  • Multiple Myeloma
  • Non-Hodgkin Lymphoma
Drug: Access to unlicensed cord blood units
N/A
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
0
November 2012
November 2012   (final data collection date for primary outcome measure)
  • INCLUSION CRITERIA:

Patients with FDA-specified indications:

  • Hematological malignancies
  • Certain lysosomal storage and peroxisomal enzyme deficiency disorders
  • Hurler syndrome (MPS I)
  • Krabbe Disease (Globoid Leukodystrophy)
  • X-linked Adrenoleukodystrophy
  • Primary immunodeficiency diseases
  • Bone marrow failure
  • Beta-thalassemia
  • Signed informed consent (and signed assent, if applicable)
  • Pediatric and adult patients of any age

EXCLUSION CRITERIA:

  • Patients who are receiving only licensed CBUs
  • Cord blood transplant recipients at international transplant centers
Both
Not Provided
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
NCT01479582
120027, 12-C-0027
Not Provided
National Institutes of Health Clinical Center (CC) ( National Cancer Institute (NCI) )
National Cancer Institute (NCI)
Not Provided
Principal Investigator: Ronald E Gress, M.D. National Cancer Institute (NCI)
National Institutes of Health Clinical Center (CC)
November 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP