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Phase 2 N=7 Treatment

Islet Cell Transplantation in Patients With Type I Diabetes With Previous Kidney Transplantation

Diabetes Mellitus, Type 1

Enrolled (actual)
7
Serious AEs
85.7%
Results posted
Apr 2017
Primary outcome: Primary: Insulin Independence. — 2 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Islet Transplantation (Drug)
Age
Adult · 18+ yrs
Sex
All
Sponsor
Rodolfo Alejandro
Primary completion
May 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Insulin Independence.
2
SECONDARY
Stimulated C-peptide Greater Than 0.5 ng/ml
6
SECONDARY
Reduction of Insulin Requirements
4
SECONDARY
Reduction in Severe Hypoglycemia, Improvement in Hypoglycemia Awareness
6

Summary

The purpose of this study is to reverse hyperglycemia and insulin dependency, by islet cell transplantation, in patients with type 1 diabetes mellitus who have a stable kidney allograft.

Eligibility Criteria

Inclusion Criteria

  • Patients between 18 and 60 years of age.
  • Patients with type 1 diabetes mellitus.
  • Patients with a renal transplant that is more than 6 months old.
  • Patients with stable renal graft function for the preceding 6 months, i.e. no episodes of rejection and changes in serum creatinine no more than 0.5 mg/dl from baseline.
  • Patients who are taking tacrolimus, sirolimus +/- steroids for maintenance immunosuppression for at least 6 months and are tolerating levels satisfactory for islet transplantation without severe complications.
  • Patients with a body mass index (BMI) of less than or equal to 26.

Exclusion Criteria

  • Stimulated or basal C-peptide > 0.3 ng/ml.
  • Patients with unstable renal function - serum creatinine greater than 0.5 mg/dl above baseline.
  • Patients with proteinuria (albuminuria > 300 mg in 24 hours +/- protein) of new onset since kidney transplantation. If proteinuria or albuminuria is thought to originate from the native kidney(s) this will not be an exclusion criterion.
  • Patients with corrected creatinine clearance of less than 40.
  • Patients weighing more than 80 kg.
  • Patients with a body mass index (BMI) of greater than 26.
  • Insulin requirement > 1.0 U/kg/d.
  • Anemia (hemoglobin: males 1.5 x normal range).
  • Unstable diabetic retinopathy.
  • Evidence of acute or chronic active Epstein-Barr virus (EBV) infection (IgM ≥ IgG). Patients will be eligible if serological testing becomes consistent with previous exposure (i.e. IgG > IgM).
  • Patients with history of malignancy or current malignancy other than non-melanomatous skin cancer, or finding of any lesions or symptoms during screening that are suspicious for malignancy, until properly investigated and ruled out.
  • Patients with elevation of prostate-specific antigen > 4 unless malignancy has been excluded.
  • Patients with unstable cardiovascular status.
  • Patients with active infections until adequately treated, unless treatment is not judged as necessary by the investigators (including, but not limited to, mild skin and nail fungal infections).
  • Patients with serological evidence of infection with HIV, human t cell lymphotropic virus 1 (HTLV 1), HTLV 2, or hepatitis B (patients with serology consistent with previous vaccination and a history of vaccination are acceptable).
  • Patients with history and/or serological evidence of hepatitis C (those patients with hepatitis C, already transplanted in this protocol will continue in this trial).
  • Positive tuberculin test (unless proof of adequate treatment for latent tuberculosis can be provided).
  • Patients with active peptic ulcer disease, gallstones, hepatic hemangioma, or portal hypertension.
  • Patients who are pregnant or breastfeeding, or who intend to procreate.
  • Patients who are sexually active females who are not:
  • post-menopausal,
  • surgically sterile, or
  • using an acceptable method of contraception (oral contraceptives, Norplant, Depo-Provera, and barrier devices combined with spermicidal gel are acceptable; condoms used alone are not acceptable).
  • Active alcohol or substance abuse; smoking in the last 6 months.
  • Patients with evidence of sensitization, i.e. panel reactive antibody (PRA) testing greater than 20%.
  • Lack of updated immunizations per current Centers for Disease Control (CDC) guidelines, as well as immunization against hepatitis B, pneumococcus, and influenza (during season), unless medically contraindicated.
  • Patients with psychogenic factors, which are judged at psychological evaluation, which make it unsafe to undergo islet transplantation, or which preclude therapeutic compliance.
  • Patients with any condition or any circumstance that would make it unsafe to undergo an islet transplant.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00315588). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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