CliniMACS® CD34+ Reagent System for Expanded Access Use
Primary Purpose
Graft-Versus-Host Disease(GVHD), Anemia Due to Disturbance of Proliferation and/or Differentiation of Hematopoietic Stem Cells, Graft Failure
Status
No longer available
Phase
Locations
United States
Study Type
Expanded Access
Intervention
CliniMACS CD34 Reagent System
Sponsored by
About this trial
This is an expanded access trial for Graft-Versus-Host Disease(GVHD) focused on measuring Graft-Versus-Host Disease(GVHD), Hematopoietic Stem Cell Transplantation., Graft failure, Graft exhaustion
Eligibility Criteria
Inclusion Criteria:
- Patients aged >18 years
- Diagnosis is graft exhaustion.
- Ability to understand and willingness to sign a written informed consent document
- Matched related or unrelated donor must consent to provide an allograft.
Exclusion Criteria:
- Symptomatic or uncontrolled cardiac failure or coronary artery disease.
- Karnofsky performance status < 60%.
Sites / Locations
- Dana Farber Cancer Institute
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT02026934
First Posted
January 2, 2014
Last Updated
November 18, 2016
Sponsor
Joseph Antin
Collaborators
Miltenyi Biomedicine GmbH
1. Study Identification
Unique Protocol Identification Number
NCT02026934
Brief Title
CliniMACS® CD34+ Reagent System for Expanded Access Use
Official Title
CliniMACS® CD34+ Reagent System for Expanded Access Use
Study Type
Expanded Access
2. Study Status
Record Verification Date
November 2016
Overall Recruitment Status
No longer available
Study Start Date
March 2013 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Joseph Antin
Collaborators
Miltenyi Biomedicine GmbH
4. Oversight
5. Study Description
Brief Summary
CliniMACs is an investigational device used to select and enrich stem cells. The device will select the stem cells with CD34+ protein. The participant will be infused with the CD34+ selected cells in the hopes that it will help the participant engraft. Engraftment is when transplanted stem cells resume production of healthy blood cells.
Detailed Description
After the screening procedures confirm that the participant is eligible to participate in the research study: If the participant takes part in this research study, the participant (and their donor) will have the following tests and procedures:
Donor Graft Collection: The participant's cell donor will undergo stem cell collection. The cells collected will be sent to the laboratory for processing.
Donor Graft Processing: In the laboratory the CliniMACS device will be used to separate the CD34+ stem cells from the other types of cells in the graft. After completing the necessary safety tests, the CD34+ selected donor graft will be ready for administration.
Donor Graft Infusion: The CD34+ selected donor graft will be infused through an intravenous (I.V.) catheter. The day of this infusion is called Day 0.
Follow-Up Visits: Approximately 3, 6 and 12 months after the donor graft infusion, the participant will return to clinic for follow-up visits. At each of the visits, the participant will have a physical exam and asked questions about your general health. The participant will also have routine blood tests performed (approximately 1 tablespoon of blood).
At times more cells are collected from a donation than are needed to do the transplantation. If your physician determines that it is preferable to administer a dose of cells that is less than the complete collection, the extra cells may be frozen and stored in our freezers for the participant's future use. If the cell counts do not improve, the participant will be given the remaining cells through an intravenous (I.V.) catheter.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Graft-Versus-Host Disease(GVHD), Anemia Due to Disturbance of Proliferation and/or Differentiation of Hematopoietic Stem Cells, Graft Failure, Delayed Graft Function
Keywords
Graft-Versus-Host Disease(GVHD), Hematopoietic Stem Cell Transplantation., Graft failure, Graft exhaustion
7. Study Design
8. Arms, Groups, and Interventions
Intervention Type
Device
Intervention Name(s)
CliniMACS CD34 Reagent System
Intervention Description
Following screening and enrollment, peripheral blood or bone marrow collection will be performed on the donor followed by subsequent CD34+ cell selection using the Miltenyi CliniMACS device. There is no limit to the number of CD34+ progenitors that can be administered. The CD34+ selected cells will be infused within 12 hours of the initiation of processing.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients aged >18 years
Diagnosis is graft exhaustion.
Ability to understand and willingness to sign a written informed consent document
Matched related or unrelated donor must consent to provide an allograft.
Exclusion Criteria:
Symptomatic or uncontrolled cardiac failure or coronary artery disease.
Karnofsky performance status < 60%.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarah Nikiforow, MD, PhD
Organizational Affiliation
Dana-Farber Cancer Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dana Farber Cancer Institute
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
12. IPD Sharing Statement
Learn more about this trial
CliniMACS® CD34+ Reagent System for Expanded Access Use
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