Pilot Trial of Allogeneic Blood or Marrow Transplantation for Primary Immunodeficiencies

Who is this study for? Patients with Immunodeficiency, Immune System Diseases
What treatments are being studied? GVHD Prophylaxis+Allo BMT
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Drug, Procedure
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Background: Allogeneic blood or marrow transplant is when stem cells are taken from one person s blood or bone marrow and given to another person. Researchers think this may help people with immune system problems.

Objective: To see if allogeneic blood or bone marrow transplant is safe and effective in treating people with primary immunodeficiencies.

Eligibility: Donors: Healthy people ages 4 or older Recipients: People ages 4-75 with a primary immunodeficiency that may be treated with allogeneic blood or marrow transplant

Design: Participants will be screened with medical history, physical exam, and blood tests. Participants will have urine tests, EKG, and chest x-ray. Donors will have: Bone marrow harvest: With anesthesia, marrow is taken by a needle in the hipbone. OR Blood collection: They will have several drug injections over 5-7 days. Blood is taken by IV in one arm, circulates through a machine to remove stem cells, and returned by IV in the other arm. Possible vein assessment or pre-anesthesia evaluation Recipients will have: Lung test, heart tests, radiology scans, CT scans, and dental exam Possible tissue biopsies or lumbar puncture Bone marrow and a small piece of bone removed by needle in the hipbone. Chemotherapy 1-2 weeks before transplant day Donor stem cell donation through a catheter put into a vein in the chest or neck Several-week hospital stay. They will take medications and may need blood transfusions and additional procedures. After discharge, recipients will: Remain near the clinic for about 3 months. They will have weekly visits and may require hospital readmission. Have multiple follow-up visits to the clinic in the first 6 months, and less frequently for at least 5 years.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 4
Maximum Age: 75
Healthy Volunteers: t
View:

• Ages greater than equal to 4

• Related donor deemed suitable and eligible and willing to donate per clinical evalations who are additionally willing to donate blood, urine, and marrow specimens for research. Related donors will be evaluated in accordance with existing Standard Policies and Procedures for determination of eligibility and suitability for clinical donation. Note that participation in this study is offered to all related donors but is not required for clinical donation, so it is possible that not all related donors will enroll on this study.

• Ages greater than equal to 18

• Unrelated donors will be evaluated in accordance with existing NMDP Standard Policies and Procedures, available at: http://bethematch.org/About-Us/Global-transplant-network/Standards/, except for the additional requirement of EBV serostatus testing. Note that participation in this study is offered to all unrelated donors but not required for clinical donation, so it is possible that not all unrelated donors will enroll on this study.

Locations
United States
Maryland
National Institutes of Health Clinical Center
RECRUITING
Bethesda
Minnesota
National Marrow Donor Program
RECRUITING
Minneapolis
Contact Information
Primary
Amy H Chai
amy.chai@nih.gov
(240) 858-3755
Backup
Dimana Dimitrova, M.D.
dimana.dimitrova@nih.gov
(240) 858-3647
Time Frame
Start Date: 2015-11-19
Estimated Completion Date: 2036-12-31
Participants
Target number of participants: 254
Treatments
Experimental: 1/ IOC Arm-Closed with amendment L (07/05/2019)
Immunosuppression Only Conditioning Arm
Experimental: 2/ RIC Arm - Closed with Amendment L (07/05/2019)
Reduced Intensity Conditioning Arm
Experimental: 3/ MAC Arm-Closed with amendment L (07/05/2019)
Myeloablative Conditioning Arm
Experimental: 4/ RIC-MMF Arm
Reduced Intensity Conditioning with MMF duration de-escalation design
No_intervention: 5/ Donor Arm
Donor
Experimental: 6/ RIC-SHORT Arm
Reduced Intensity Conditioning with shortened duration and dose-reduced PTCy
Sponsors
Leads: National Cancer Institute (NCI)

This content was sourced from clinicaltrials.gov

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