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Taking people in United StatesPhase 1

Tests a pig kidney transplant in adults with end-stage kidney disease

Tests whether a pig kidney can work without dialysis in adults with kidney failure.

Plain-language title generated from the registry record
Registry title: Study of ChoironeX GalKO Porcine Thymokidney Xenotransplantation in End-Stage Renal Disease

Key facts

Where
New York, United StatesSee the 2 sites
Phase
Phase 1

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 70 years old?

Source: NCT07696962, who can take part

Where in United States

  • New YorkNew York, United StatesNot yet recruiting
  • NYU Langone HealthNew York, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Xeno Holdings (US), LLC dba ChoironeX
Trial code
NCT07696962
Record updated
10 November 2026
Original description
The goal of this clinical trial is to learn if a GalKO Porcine Thymokidney can maintain renal function, without the need for dialysis, after transplantation into adult subjects with End Stage Renal Disease.Read full original descriptionShow less

Phase 1 Study of ChoironeX GalKO Porcine Thymokidney Xenotransplantation in End-Stage Renal Disease

The goal of this clinical trial is to learn if a GalKO Porcine Thymokidney can maintain renal function, without the need for dialysis, after transplantation into adult subjects with End Stage Renal Disease.

Inclusion: ESRD receiving hemodialysis or peritoneal dialysis for ≥6 months; Eligible for kidney transplantation per site criteria; <50% likelihood of receiving a standard deceased-donor kidney transplant within 12 months; Blood type and immunologic compatibility with study transplant confirmed by testing; EBV seropositive; Up to date on recommended vaccinations for immunocompromised individuals; Willing to use protocol-required contraception; Able to provide informed consent and comply with lifelong follow-up.

Exclusion: Requirement for multi-organ transplantation; Polycystic kidney disease without prior native nephrectomy; Current drug or alcohol misuse; Malignancy within 5 years prior to enrollment, excluding adequately treated non-melanoma skin cancer; Current systemic immunosuppressive therapy (excluding permitted corticosteroids); Participation in another interventional drug trial within 60 days prior to enrollment; Kidney disease with high risk of post-transplant recurrence; History of non-adherence to medical treatment; Significant uncontrolled psychiatric illness; Serious non-renal illness with life expectancy <1 year; Known hypercoagulable disorder; Uncontrolled hypertension or hemodynamic instability at enrollment; Clinically significant cardiovascular disease, including poorly controlled coronary artery disease, reduced left ventricular function, recent myocardial infarction or cardiac intervention, or clinically significant arrhythmia requiring treatment; Serious liver disease or impaired liver function; Active infection at time of transplantation; Positive serology for hepatitis B, hepatitis C, or HIV; Current, active, or untreated tuberculosis; Known severe hypersensitivity to a required study medication with no acceptable alternative; Diabetes mellitus with poor glycemic control (HbA1c >10%); Living donor available who is ABO-incompatible; Unable or unwilling to comply with study procedures; Identified as vulnerable by psychological assessment; Inadequate social support or caregiver unavailable/unwilling; BMI <16 or >35 kg/m²; Pregnant or breastfeeding.

ClinicalTrials.gov NCT07696962