Overview
Combined Blood Stem Cell and Kidney Transplant of One Haplotype Match Living Donor Pairs.
Status:
Recruiting
Recruiting
Trial end date:
2024-06-14
2024-06-14
Target enrollment:
0
0
Participant gender:
All
All
Summary
The Stanford Medical Center Program in Multi-Organ Transplantation and the Division of Bone marrow Transplantation are enrolling patients into a research study to determine if donor stem cells given after a living related one Haplotype match kidney transplantation will change the immune system such that immunosuppressive drugs can be completely withdrawn.Phase:
Phase 1Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Stanford UniversityCollaborator:
National Heart, Lung, and Blood Institute (NHLBI)
Criteria
Inclusion Criteria:1. All consenting adults who are 18 to 60 years, living donor transplant candidates and
have a haplotype related living donor or > 2 HLA antigen matched, unrelated, living
donor (including at least one HLA-DR antigen match plus at least one antigen match of
either HLA-A or HLA-B).
2. Patients who agree to participate in the study and sign an Informed Consent.
3. Patients who have no known contraindication to administration of rabbit ATG or
radiation.
4. Males and females of reproductive potential who agree to practice a reliable form of
contraception for at least 24 months post-transplant.
5. ABO compatible.
Exclusion Criteria:
1. Previous treatment with rabbit ATG or a known allergy to rabbit proteins.
2. History of malignancy with the exception of non-melanoma skin malignancies.
3. Pregnant women or nursing mothers.
4. Serological evidence of HIV, Hepatitis B or Hepatitis C infection.
5. Seronegative for Epstein-Barr virus, if donor is seropositive.
6. Leukopenia (with a white blood cell count < 3000/mm3) or thrombocytopenia (with a
platelet count < 100,000/mm3).
7. Panel Reactive Antibody greater than 80% or demonstration of donor specific antibody
(DSA).
8. Prior organ transplantation.
9. High risk of primary kidney disease recurrence (e.g atypical HUS). However, patients
with primary FSGS will not be excluded.