Calcineurin Inhibitor-free, Steroid-free Immunosuppressive Regimen in Simultaneous Islet-Kidney Transplantation for Uremic Type 1 Diabetic Patients

This is an interventional treatment trial for Islets of Langerhans Transplantation Read More

Inclusion Criteria:

• Subjects will include those with Type 1 Diabetes Mellitus, undergoing kidney transplantation, and:

  • are closely followed by a primary care provider and/or endocrinologist for >6 months prior to enrollment in the trial
  • do not have psychogenic factors which preclude therapeutic compliance
  • have a fasting C-peptide of <0.2 ng/mL• have diabetes for >5 years • are between 18 and 65 years of age
  • have a creatinine clearance of less than 20 mL/min
  • have a body mass index of less than or equal to 28
  • In the case of women of childbearing potential (WOCBP), must have a negative pregnancy test and avoid pregnancy throughout the study and 8 weeks after final dose of study drug.
  • WOCBP must use two adequate methods of contraception.
  • A male subject of fathering potential must use an adequate method of contraception to avoid conception throughout the study and for up to 8 weeks after the last dose of study drug to minimize the risk of pregnancy.

Exclusion Criteria:

• Untreated proliferative diabetic retinopathy

  • HgbA1C >12
  • creatinine clearance > 20 ml/minute
  • presence of panel reactive antibodies (PRA) >20% (per CDC-based assay)
  • malignancy or previous malignancy, except for adequately treated skin cancers (basal cell or squamous cell carcinoma) within the past 5 years
  • sensitivity to iodine and/or shellfish (re: Iothalamate-based GFR testing)
  • x-ray evidence of pulmonary infection
  • active infections
  • active peptic ulcer disease, gall stones, hemangioma, cirrhosis or portal hypertension
  • serological evidence of HIV, HBSAg or HCV
  • abnormal liver function tests (elevated AST and ALT > 2x upper limit of normal)
  • anemia (hemoglobin) <9 gm/dl
  • serum triglycerides >200 mg/dl
  • serum cholesterol >240 mg/dl
  • body mass index above 28
  • unstable cardiovascular status (including positive stress echocardiography if >age 35); severe coexisting cardiac disease, myocardial infarction within the 6 months prior to enrollment in the study, left ventricular ejection fraction of <30%, or evidence of ongoing ischemia
  • prostate specific antigen (PSA) >4 in males >40 years old or with family history of prostate cancer
  • pregnancy or breastfeeding
  • sexually-active females who are not: a) post-menopausal, b) surgically sterile, or c) not using an acceptable method of contraception (oral contraceptives, Norplant, Depo-Provera, and barrier devices are acceptable; condoms used alone are not acceptable)
  • alcohol abuse, substance abuse or smoking within the previous 6 months
  • insulin requirement >1.5 u/kg/day
  • negative for Epstein-Barr virus by IgG determination
  • history of factor V deficiency
  • acute or chronic pancreatitis
  • recurrent attenuated vaccine(s) within the previous 2 months
  • use of an investigational agent within the past 4 weeks
  • sexually active, fertile men not using effective birth control, if their partners are WOCBP
  • prisoners, or subjects who are involuntarily incarcerated
  • subjects who are compulsorily detained for treatment of either a psychiatric or physical (eg, infectious disease) illness
  • Previous kidney transplant or previous non-renal transplant
  • kidney transplant from expanded criteria donor (ECD)
  • kidney cold ischemic time projected to be > 20 hours
  • currently receiving immunosuppressive agents for autoimmune disease or other conditions or have comorbidities that treatment with such agents are likely during the trial
  • any condition or circumstance that makes it unsafe to undergo an islet cell or kidney transplant