Expanded Access to T-cell Depleted Haplo-Identical Stem Cells for Patients Receiving Haplo-Identical and Unrelated Cord Blood Transplants

Trial statusAvailable
Trial phaseNot listed
Trial typeExpanded Access
Biological sexAll
AgeUp to 65
SponsorJoanne Kurtzberg, MD

About this trial

The objective of this study is to make T-cell depleted stem cells from a family member who is a half match (haplo-identical) available on an expanded access basis to patients receiving one or two unrelated cord blood transplants who are at a higher risk of not engrafting in a safe amount of time. The purpose of the related stem cells is to give the bone marrow a "jump start" towards recovery. Ultimately, the cord blood cells will grow and permanently rescue the bone marrow.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Have a consenting related haplo-identical (3/6, 4/6, or 5/6 if DRB1 mismatch) stem cell donor.

Have one or two available 4, 5, or 6/6 antigen matching unrelated UCB unit(s) that will deliver a total cell dose >3.0 x 10e7 cells/kg. Patients who do not have a single UCB unit that will deliver the minimum required cell dose, two partially HLA-matched UCB units which together meet the minimum cell dose requirement, can be used for 1 transplant. These units must be HLA-matched minimally at 4 of 6 HLA-A and B (at intermediate resolution by molecular typing) and DRB1 (at high resolution by molecular typing) loci with the patient, and HLA-matched at 3 of 6 HLA- A, B, DRB1 loci with each other (using same resolution of HLA typing as indicated above). There is no limitation on maximum cell dose.

Have a high risk or refractory malignancy, or non-malignant disorder amenable to stem cell transplantation therapy.

Meet eligibility requirements for allogeneic transplant per institutional standard practices.

Disqualifiers

Have a consenting 8/8 or 10/10 allele matched, consenting, related or unrelated hematopoietic stem cell transplant (HSCT) donor.

Have a life expectancy of less than 3 months.

Have uncontrolled infections at time of cytoreduction.

Trial design

Treatments tested in this trial

  • CliniMACS CD34 Reagent System

    Biological/Vaccine

    The CliniMACS CD34 Reagent System is a medical device that is used in vitro to select and enrich CD34+ cells from heterogeneous hematologic cell populations for transplantation in cases where this is clinically indicated.

Treatment groups

No treatment groups listed

Trial outcomes

This trial has no outcomes listed.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Joanne Kurtzberg, MD

Lead sponsor

Duke University

Sponsor institution

Duke University

Collaborator

Miltenyi Biotec, Inc.

Collaborator