Induction of Donor-Specific Tolerance in Recipients of Live Donor Stem Cell Infusion (Compassionate Use)
NCT ID: NCT02051673
Last Updated: 2022-07-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Brief Summary
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Detailed Description
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Conditions
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Interventions
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Biological/Vaccine: Enriched Hematopoetic Stem Cell Infusion
Enriched Hematopoetic Stem Cell Infusion
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
65 Years
ALL
No
Sponsors
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Northwestern University
OTHER
Talaris Therapeutics Inc.
INDUSTRY
Responsible Party
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Principal Investigators
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Suzanne T Ildstad, MD
Role: STUDY_DIRECTOR
Talaris Therapeutics Inc.
Locations
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Northwestern Memorial Hospital
Chicago, Illinois, United States
Countries
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Other Identifiers
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ICT-7392-Compassionate Use
Identifier Type: -
Identifier Source: org_study_id
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