BMT and High Dose Post-Transplant Cyclophosphamide for Chimerism Induction and Renal Allograft Tolerance

• Status: Terminated
• Trial end date: 2017-09-06
• Target enrollment: 0
• Participant gender: All

Summary

The primary objective of this study is to assess the ability of bone marrow transplantation (BMT) and high-dose post-transplantation cyclophosphamide (PT/Cy) to induce renal allograft tolerance and thus enable discontinuation of immunosuppressive therapy in haploidentical living related donor renal transplant recipients.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: National Institute of Allergy and Infectious Diseases (NIAID)
• Collaborator: Immune Tolerance Network (ITN)
• Treatments: Acetaminophen; Antilymphocyte Serum; Cyclophosphamide; Diphenhydramine; Fludarabine; Fludarabine phosphate; Lenograstim; Mesna; Methylprednisolone; Methylprednisolone acetate; Methylprednisolone Hemisuccinate; Mycophenolate mofetil; Mycophenolic Acid; Prednisolone; Prednisolone acetate; Prednisolone hemisuccinate; Prednisolone phosphate; Prednisone; Promethazine; Thymoglobulin

Criteria

Inclusion Criteria:

• Recipient participants must meet all of the following criteria to be eligible for this study:

• Recipient of a first renal allograft from an Human Leukocyte Antigen (HLA)-haploidentical, living related donor. The donor and recipient must be HLA identical for at least one allele (using high resolution DNA based typing) at the following genetic loci: HLA-A, HLA-B, HLA-C and HLA-DRB1. Fulfillment of this criterion shall be considered sufficient evidence that the donor and recipient share one HLA haplotype.

• Age 18 to 65 years.

• Single solid organ recipients (kidney only).

• Blood Group System (ABO) compatibility with donor.

• Donor-Specific Antibody (DSA) will be assessed by the local laboratory 30 days or less prior to transplant using solid phase micro particle technology (by Luminex® phenotype panel or Luminex single antigen bead test.) The following criteria apply:

• Participants without detectable DSA will be deemed eligible if they meet other entry criteria.

• Participants with detectable DSA and a positive flow cytometric crossmatch may undergo de-sensitization per standard of care if they are cytotoxic crossmatch negative. Such participants must demonstrate a negative flow cytometric crossmatch by day -9 in order to receive the first dose of study therapy (ATG). Participants who do not demonstrate an acceptable response to de-sensitization by day -9 will be considered screen failures and will be terminated from the study.

• Participants with a positive cytotoxicity crossmatch will be excluded.

• No known history of anti-HLA antibodies. Recipients with low- level anti-HLA antibodies not considered to be clinically significant may be eligible, following consultation with the Protocol Chairs, the local HLA Laboratory Director, the NIAID Medical Monitor and the ITN Clinical Trial Physician.

• Negative T and B cell flow crossmatches with the designated donor; as assessed by local laboratories. If one or more of the crossmatches is positive, the participant will be considered a screen failure unless combined results of antibody and cross match testing implicate a non-HLA antibody as the cause of the positive flow crossmatch. In this case, the Protocol Chair must approve the participant as a screening success after consultation with the local HLA Laboratory Director.

• Normal estimated left ventricular ejection fraction and no history of ischemic heart disease requiring revascularization, unless cleared by a cardiologist.

• Forced expiratory volume (FEV1) and forced vital capacity (FVC) > 40% of predicted at the screening visit.

• Serological evidence of prior Epstein-Barr virus (EBV) infection as documented by positive IgG and negative IgM antibodies against EBV.

• For women of childbearing potential, a negative serum or urine pregnancy test with sensitivity less than 50 Milli-International unit (mIU)/m within 72 hours before the start of study medication.

• Use of two forms of contraception with less than a 5% failure rate or abstinence by all transplanted participants for 18 months after the first dose of study therapy. For the first 60 days post-transplant, recipients should be encouraged to use non-hormonal contraceptives due to the potential adverse effect of hormones on bone marrow engraftment.

• Ability to receive oral medication.

• Ability to understand and provide informed consent.

• All participants must demonstrate a negative QuantiFERON® (QFT) assay result within 52 weeks of transplant regardless of Purified Protein Derivative (PPD) status. Participants with a positive QFT assay will not be eligible for the study unless they have completed treatment for latent TB and have a negative chest x-ray. QFT testing done within 52 weeks before transplant is acceptable as long as there is documentation of the results. Prior recipients of a Bacillus Calmette-Guérin (BCG) vaccination are not exempt.

• Donor participants must meet all of the following criteria to be eligible for this study:

• HLA-haploidentical, first-degree relatives or half-siblings of the recipient participant at the allele or allele group. The donor and recipient must be HLA identical for at least one allele (using high resolution DNA based typing) at the following genetic loci: HLA-A, HLA-B, HLA-C, and HLA-DRB1. Fulfillment of this criterion shall be considered sufficient evidence that the donor and recipient share one HLA haplotype.

• Age 18 to 65 years.

• Creatinine clearance >80 ml/minute as measured from a 24 hour urine collection within 26 weeks of the screening visit. If a serum creatinine drawn at the screening visit is > 20% higher than the serum creatinine drawn at the time of the 24 urine collection, the creatinine clearance must be re-evaluated by a repeat 24 hour urine test. If the new value is ≤80mg/dL the donor will be excluded.

• Meets institutional selection criteria for organ and bone marrow donation.

• Ability to understand and provide informed consent for all study procedures including kidney transplant and bone marrow harvest.

• Serologic evidence of prior EBV infection as documented by positive Immunoglobulin G (IgG) and negative Immunoglobulin M (IgM) antibodies against EBV.

Exclusion Criteria:

• Recipient subjects who meet any of the following criteria will not be eligible for this study:

• Underlying renal disease with a high risk of disease recurrence in the transplanted kidney, including:

1. Focal segmental glomerulosclerosis (FSGS).

2. Type I or II membranoproliferative glomerulonephritis.

3. Hemolytic-uremic syndrome/thrombotic thrombocytopenic purpura.

• Clinically important genital/urinary tract dysfunction.

• Body mass index (BMI) > 40.

• Women who are breastfeeding.

• History of cancer within the last 5 years, except for nonmelanoma skin cancer, stage 1 renal cell carcinoma, stage 1 prostate cancers cured by local resection and any curatively treated carcinomas in situ.

• History of positive HIV-1 or HIV-2 serologies or nucleic acid test.

• Evidence of prior hepatitis B infection as evaluated by hepatitis B surface antigen (HBsAg), total hepatitis B core antibody (anti-HBc IgM and IgG) and Hepatitis B surface antibody (anti-HBsAb).

Subjects demonstrating any one of the following will be excluded:

• Positive hepatitis B surface antigen (HBsAg) or

• Positive anti-HBc IgM.

• Positive anti-HBc IgG.

• Positive Hepatitis B virus (HBV) Polymerase chain reaction (PCR).

• Positive anti-hepatitis C (HCV) antibodies and a positive serum HCV RNA PCR. All positive HCV antibody results must be assessed by an Electroimmunoassay (EIA) assay and confirmed by a quantitative serum HCV RNA assay. Participants with positive HCV antibodies but undetectable serum HCV RNA may be considered for eligibility. Participants with negative anti-HCV antibodies but unexplained liver enzyme abnormalities must undergo a quantitative serum RNA assay to rule out false negative HCV serologies.

• History of active Tuberculosis (TB).

• Any active, severe local or systemic infection at the screening visit.

• Autoimmune disease requiring immunosuppressive drugs for maintenance.

• Use of investigational drug, other than the study medications specified by the protocol, within 30 days of transplantation.

• Receipt of a live vaccine within 30 days of receipt of study therapy.

• The presence of any medical condition that the Investigator deems incompatible with participation in the trial.

• Donor subjects who meet any of the following criteria will not be eligible for this study:

• History of type I or type II diabetes mellitus.

• History of severe cardiovascular disease, defined as New York Heart Association Class III or IV.

• History of blood product donation to recipient.

• History of positive HIV-1 or HIV-2 serology or nucleic acid test.

• Evidence of prior hepatitis B infection.

Subjects demonstrating any one of the following will be excluded:

• Positive hepatitis B surface antigen (HBsAg) or

• Positive anti- hepatitis B core antigen (HBc) IgM.

• Positive anti-HBc IgG.

• Positive HBV PCR

• Positive anti-hepatitis C (HCV) antibodies and a positive serum HCV RNA PCR. All positive HCV antibody results must be assessed by an EIA assay and confirmed by a quantitative serum HCV RNA assay. Participants with positive HCV antibodies but undetectable serum HCV RNA may be considered for eligibility. Participants with negative anti-HCV antibodies but unexplained liver enzyme abnormalities must undergo a quantitative serum RNA assay to rule out false negative HCV serologies.

• Autoimmune disease requiring immunosuppressive drugs for maintenance.

• The presence of any medical condition that the Investigator deems incompatible with participation in the trial.