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Induction of Donor-Specific Tolerance in Recipients of Live Donor Stem Cell Infusion (Compassionate Use)

T

Talaris Therapeutics

Status

Conditions

Renal Failure

Treatments

Biological: Biological/Vaccine: Enriched Hematopoetic Stem Cell Infusion

Study type

Expanded Access

Funder types

Other
Industry

Identifiers

NCT02051673
ICT-7392-Compassionate Use

Details and patient eligibility

About

Four subjects were treated under compassionate use provisions under this study with facilitating cell therapy (FCRx)

Full description

Four subjects were treated under compassionate use provisions under this study with facilitating cell therapy (FCRx) and living donor kidney transplant.

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient must be between the ages of 18 and 65 years and meet the institution's criteria for renal transplantation for end-organ failure
  • Patient is receiving first renal transplant
  • Patient is receiving a renal transplant only
  • The crossmatch is negative between donor and recipient
  • Women who are of child bearing potential must have a negative pregnancy test (urine test is acceptable) within 48 hours of initiating total body irradiation (TBI) and agree to use reliable contraception for 1 year following transplant
  • Potential donors who are women of child bearing potential must have a negative pregnancy test (urine test is acceptable) within 48 hours prior to receiving Granulocyte colony-stimulating factor (G-CSF)
  • No evidence of donor-specific antibody presently or historically

Exclusion criteria

  • Clinically active bacterial, fungal, viral or parasitic infection
  • Pregnancy
  • Clinical or serologic evidence of viral infection which would preclude the recipient from receiving a kidney transplant
  • Previous radiation therapy at a dose which would preclude TBI
  • Positive crossmatch between donor and recipient
  • Evidence for immunologic memory against donor
  • BMI >35 or <18
  • Re-transplant
  • Positive serologies for hepatitis B virus (HBV), hepatitis C virus (HCV), HIV

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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