Skip to main content
OpenTrials
Recruiting

NCT Number: NCT04571203

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

This is a single arm phase 1 non randomized dose finding study for safety, feasibility and efficacy of deceased donor vertebral body (VB) marrow cell infusion and kidney transplantation.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Stanford University, Palo Alto, California, United States

Loading trial locations.

About this study

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Subjects will be withdrawn from the immunosuppression if they have met the withdrawal criteria.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

RECIPIENT INCLUSION CRITERIA:

  • Patient is ≥ 18 years old, and <65 years of age.
  • Has End Stage Renal Disease (ESRD) and is a de novo kidney transplant candidate part Stanford standard of care.
  • Listed with the Organ Procurement and Transplantation Network (OPTN) for deceased donor transplantation.
  • A serotypic (Human Leucocyte Antigen) HLA match with the donor of a least 1 locus in A, B or DR.
  • Males and females of reproductive potential who agree to practice a reliable form of contraception for at least 1 year post transplant.
  • Females have a negative serum pregnancy test.
  • Ability to understand and the willingness to sign a written informed consent document. Patients must have signed informed consent to participate in the trial.
  • No known contraindication to administration of rabbit ATG or low dose irradiation.

DONOR INCLUSION CRITERIA:

  • Brain dead donor aged ≥ 16 and ≤ 55
  • Organ Procurement Organization (OPO) consent for vertebral body procurement
  • Organ Procurement Organization consent for research
  • Projected cold ischemia time <24 hours.

Exclusion criteria

RECIPIENT EXCLUSION CRITERIA:

  • Known allergy to rabbit protein.
  • History of malignancy with the exception of non melanoma skin malignancy.
  • Pregnant woman or nursing mother.
  • Body weight >90kg or BMI >35.
  • 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.
  • EBV (Epstein Bar Virus)Ab positive donor to EBV Ab negative recipient.
  • Active bacterial, viral or fungal infection defined as currently taking medication for the infection.
  • Leukopenia (white blood cell count < 3000/mm3) or thrombocytopenia (with a platelet count < 100,000/mm3).
  • 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.
  • Concern for alcohol or other substance abuse.
  • Kidney disease at high risk for post transplant recurrence: aHUS (atypical hemolytic- uremic syndrome) and C3 glomerulopathy
  • Panel reactive antibody (PRA) >80%.
  • Positive donor specific antibody (DSA).
  • Prior or combined organ transplant.
  • Patients with >5 pack year smoking history, smoking within 10 years of enrollment, or first degree relative with lung cancer.

DONOR EXCLUSION CRITERIA:

  • History of malignancy with the exception of non melanoma skin malignancy.
  • History of autoimmune disease.
  • Known medical diagnosis of Zika virus infection within the prior 6 months, including post mortem screening.
  • Serological evidence of HIV, Hepatitis B (surface antigen positive), or Hepatitis C infection.
  • Evidence of systemic infection.
  • Kidney Donor Profile Index (KDPI) > 70%.

Treatment and study plan

Combined Deceased Donor Kidney and Hematopoietic Cell Transplants

Biological

This combined kidney and hematopoietic cell transplants with a conditioning regimen with irradiation and ATG creates an environment of immune-tolerance. This promotes hematopoietic cell engraftment.

Other names: Radiation

Primary outcomes

  1. Number of patients out of the total patients enrolled who received both the kidney and the bone marrow from the same donor.

    Time frame: 6 months

  2. Determine the dose of TBI that will support donor CD3 Tcell chimerism between 30-75% at 45 days post infusion

    Time frame: day 45

    TBI dose in cGy associated with donor Tcell chimerism of >30 % immunosuppressive drug monotherapy.

Secondary outcomes

  1. Number of patients who develop GVHD, all grades and types, within 60 months of kidney transplant

    Time frame: 60 months

  2. Number of patients with either bacterial, viral or fungal infection within 12 months post transplant .

    Time frame: 12 months

  3. Serum Creatinine

    Time frame: up to 60 months

  4. Panel-Reactive Antibody (PRA)

    Time frame: Baseline, month 9, and month 12

    Report % of PRA on all participants

  5. Donor-Specific Antibody (DSA)

    Time frame: Baseline, month 9, and month 12

    Report percentage of patients that develop DSA

  6. Percentage of subjects on immunosuppressive medications after an eighteen month post transplant till month 60.

    Time frame: 60 months

  7. Persistence of donor chimerism >1%

    Time frame: 3,6,9,12,15,18,24,48,60 months

    Percentage of patients with donor chimerism (any lineage)

Study contacts

Contact information is provided by the study sponsor or research team.

Anika Tahsin, BS

CONTACT

[email protected]

Carlos Lazarte, B.A.

CONTACT

[email protected]

6505548610

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Registry information

Official study title

Phase I Study of Combined Deceased Donor Kidney and Hematopoietic Cell Transplants Using a Regimen to Promote Hematopoietic Cell Engraftment

Important dates

Study start
2022
Primary completion
2027
Study completion
2029
First posted
Sep 30, 2020
Registry last updated
Jul 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.