Delayed Tolerance Through Mixed Chimerism

• Status: Not yet recruiting
• Trial end date: 2029-12-01
• Target enrollment: 0
• Participant gender: All

Summary

This study will examine the safety and effectiveness of a bone marrow transplant after kidney transplant (from either a living or deceased donor). An investigational medication and other treatments will be given prior to and after the transplant to help protect the transplanted kidney from being attacked by the body's immune system

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Massachusetts General Hospital
• Collaborators: ITB-Med LLC; Ossium Health, Inc.
• Treatments: Cyclophosphamide; Fludarabine; Rituximab

Criteria

Recipient Inclusion Criteria

1. Male or female 18-65 years of age.

2. Kidney transplant recipients from either LD or DD, with cryo-preserved HSCs available, good renal function (GFR>45 ml/min/1.73m2), normal current allograft biopsy, and no history of documented rejection episodes.

3. First or second renal transplant.

4. Use of FDA-approved methods of contraception (those with less than a 3% failure rate) by all recipients from the time that study treatment begins until 104 weeks (24 months) after renal transplantation. (For further information on FDA- approved methods of contraception, see https://www.fda.gov/media/150299/download

5. Ability to understand and provide informed consent.

6. Serologic evidence of prior exposure to EBV.

7. Negative COVID-19 test during screening and two days prior to HSC transplantation (HSCT).

Deceased Donor (DD)

1. Male or female 18-70 years of age.

2. Consent to donate vertebral bones is obtained from the donor family.

3. HSCs are successfully cryopreserved and saved >2X106/kg (CD34+ cells) of the recipient.

4. Acceptable laboratory parameters (hematology in normal or near-normal range. Liver function <2 times the upper limit of normal, and normal creatinine)

5. Negative for viral infection with HbsAg, HIV, HCV, or HTLV-1

6. Negative COVID-19 test at the time of HSC procurement.

Living Donor (LD)

1. Willingness to provide HSCs by leukapheresis or bone marrow aspiration.

2. Negative serologic pregnancy test for females of childbearing potential

3. Good general health as per conventional evaluation for kidney donation.

4. Acceptable laboratory parameters (hematology in normal or near normal range. Liver function <2 times the upper limit of normal, and normal creatinine)

5. Negative for viral infection with HbsAg, HIV, HCV, or HTLV-1.

6. Cardiac/pulmonary function within normal limits (CXR, ECG).

7. Ability to understand and provide informed consent.

8. Meets standard institutional criteria for PBSC collection.

9. Negative COVID-19 test during screening and two days prior to PBSC collection.

Recipient Exclusion Criteria

1. ABO blood group-incompatible renal allograft.

2. Evidence of anti-HLA antibody (donor specific with an MFI >1000) as assessed by routine methodology (Luminex)

3. Previous history of biopsy proven rejection.

4. Persistent Leukopenia (WBC less than 2,000/mm3) or thrombocytopenia (<100,000/mm3).

5. Seropositivity for HIV-1, hepatitis B surface or core antigen, or hepatitis C virus (confirmed by hepatitis C virus RNA).

6. Active infection

7. Left ventricular ejection fraction < 40% as determined by TTE or clinical evidence of heart failure.

8. Forced expiratory volume FEV1 or DLCO < 50% of predicted.

9. Lactation or pregnancy.

10. History of cancer other than basal cell carcinoma of the skin or carcinoma in situ of the cervix.

11. Underlying renal disease etiology with high risk of disease recurrence in the transplanted kidney (such as focal segmental glomerulosclerosis). Autoimmune diseases such as Lupus and Thrombotic Thrombocytopenic Purpura.

12. Enrollment in other investigational drug studies within 30 days prior to enrollment.

13. Abnormal (>2 times lab normal) values for (a) liver function chemistries (ALT, AST, AP), (b) bilirubin, (c) coagulation studies (PT, PTT), or any patients on chronic anticoagulation therapy.

14. Allergy or sensitivity to any component of Siplizumab, fludarabine, CP, tacrolimus, MMF or rituximab.

15. Any medical condition that the investigator deems incompatible with participation in the trial. This includes a history of alcohol abuse or illicit drug use/dependence.

16. Non-insulin dependent diabetes (NIDDM) without good blood glucose control (HbA1c<7). Severe retinopathy, gastroparesis, or severe neuropathy which prevent subject's normal independent daily activities.