ClinConnect ClinConnect Logo
Search / Trial NCT04571203

Kidney and Hematopoietic Cell Transplants Using a Regimen to Promote Hematopoietic Cell Engraftment

Launched by STANFORD UNIVERSITY · Sep 25, 2020

Trial Information

Current as of June 26, 2025

Enrolling by invitation

Keywords

ClinConnect Summary

Patients will undergo a standard of care deceased donor kidney transplant and thereafter the recipient will receive TLI (Total Lymphoid Irradiation)/single low dose Total Body Irradiation, ATG (Anti-Thymocyte Globulin) conditioning, followed by an infusion of whole bone marrow cells harvested from the same donor vertebral bodies. Patients will be receive standard of care doses of steroids, MMF and tacrolimus as part of their transplant immunosuppression.

Subjects will be withdrawn from the immunosuppression if they have met the withdrawal criteria.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • RECIPIENT INCLUSION CRITERIA:
  • 1. Patient is ≥ 18 years old, and \<65 years of age.
  • 2. Has End Stage Renal Disease (ESRD) and is a de novo kidney transplant candidate part Stanford standard of care.
  • 3. Listed with the Organ Procurement and Transplantation Network (OPTN) for deceased donor transplantation.
  • 4. A serotypic (Human Leucocyte Antigen) HLA match with the donor of a least 1 locus in A, B or DR.
  • 5. Males and females of reproductive potential who agree to practice a reliable form of contraception for at least 1 year post transplant.
  • 6. Females have a negative serum pregnancy test.
  • 7. Ability to understand and the willingness to sign a written informed consent document. Patients must have signed informed consent to participate in the trial.
  • 8. No known contraindication to administration of rabbit ATG or low dose irradiation.
  • DONOR INCLUSION CRITERIA:
  • 1. Brain dead donor aged ≥ 16 and ≤ 55
  • 2. Organ Procurement Organization (OPO) consent for vertebral body procurement
  • 3. Organ Procurement Organization consent for research
  • 4. Projected cold ischemia time \<24 hours.
  • Exclusion Criteria:
  • RECIPIENT EXCLUSION CRITERIA:
  • 1. Known allergy to rabbit protein.
  • 2. History of malignancy with the exception of non melanoma skin malignancy.
  • 3. Pregnant woman or nursing mother.
  • 4. Body weight \>90kg or BMI \>35.
  • 5. Evidence of HIV 1/2 antibody (Ab), HTLV 1 and HTLV 2 Ab (Human T-Lymphotropic Virus), Hepatitis B sAg (surface antigen), Hepatitis C Ab, or positive syphilis screen.
  • 6. EBV (Epstein Bar Virus)Ab positive donor to EBV Ab negative recipient.
  • 7. Active bacterial, viral or fungal infection defined as currently taking medication for the infection.
  • 8. Leukopenia (white blood cell count \< 3000/mm3) or thrombocytopenia (with a platelet count \< 100,000/mm3).
  • 9. Psychiatric disorder(s) or psychosocial circumstance(s) which in the opinion of the Stanford Transplant team caring for this potential patient would place the patient at an unacceptable risk.
  • 10. Concern for alcohol or other substance abuse.
  • 11. Kidney disease at high risk for post transplant recurrence: aHUS (atypical hemolytic- uremic syndrome) and C3 glomerulopathy
  • 12. Panel reactive antibody (PRA) \>80%.
  • 13. Positive donor specific antibody (DSA).
  • 14. Prior or combined organ transplant.
  • 15. Patients with \>5 pack year smoking history, smoking within 10 years of enrollment, or first degree relative with lung cancer.
  • DONOR EXCLUSION CRITERIA:
  • 1. History of malignancy with the exception of non melanoma skin malignancy.
  • 2. History of autoimmune disease.
  • 3. Known medical diagnosis of Zika virus infection within the prior 6 months, including post mortem screening.
  • 4. Serological evidence of HIV, Hepatitis B (surface antigen positive), or Hepatitis C infection.
  • 5. Evidence of systemic infection.
  • 6. Kidney Donor Profile Index (KDPI) \> 70%.

About Stanford University

Stanford University is a prestigious academic institution renowned for its cutting-edge research and innovation in healthcare and medicine. As a clinical trial sponsor, Stanford leverages its extensive resources, including a collaborative network of world-class researchers and state-of-the-art facilities, to advance medical knowledge and improve patient care. The university is committed to conducting rigorous, ethical research that adheres to the highest standards of scientific integrity, fostering an environment where groundbreaking discoveries can translate into effective clinical applications. Through its clinical trials, Stanford aims to address critical health challenges and contribute to the development of novel therapies and treatment strategies.

Locations

Palo Alto, California, United States

Patients applied

0 patients applied

Trial Officials

Robert Lowsky, MD

Principal Investigator

Stanford University

Stephan Busque, MD

Principal Investigator

Stanford University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials