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Completed

NCT Number: NCT00888628

Study of Islet Transplantation in Type 1 Diabetic Kidney Transplant Recipients

The purpose of the study is to learn if islet transplantation is an effective treatment for Type 1 diabetes in people who have had a kidney transplant.

The primary objectives of the study are:

- To set up islet transplantation in patients who have had a kidney transplant and who are using an immunosuppressive regimen that works

The Secondary objective of the study is:

* To find out if successful islet transplantation leads to improved metabolic control and reduced renal complication from diabetes

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

About this study

Patients will receive (an) infusion(s) of in vitro cultured islets with the goal of achieving insulin independence. For the first islet transplant, patients will receive induction therapy with rabbit anti-thymocyte globulin (ATG, 5 doses) and will remain on their maintenance immunosuppression regimen already in place for their renal allograft. Induction therapy for subsequent transplants will be 2doses of basiliximab.

All patients will receive Etanercept to promote engraftment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female subjects
  • Age 18 to 70 years of age
  • Have insulin dependent Diabetes Mellitus Type 1
  • Are post-renal transplant on maintenance immunosuppression with stable renal function
  • HbA1c > 7.5% or < 7.5% and hypoglycemia unawareness

Exclusion criteria

  • Weight more than 90 kg
  • Insulin requirement > 60 Units/day
  • Other (non-kidney) organ transplants except prior failed pancreatic graft.
  • Untreated or unstable proliferative diabetic retinopathy
  • Presence of de novo antibody production since the renal allograft or either Class I or Class II panel-reactive anti-HLA antibodies
  • Active infection
  • Negative screen for Epstein-Barr virus (EBV)
  • Any history of malignancy except for completely resected squamous or basal cell carcinoma of the skin
  • History of Factor V Leiden mutation
  • Any coagulopathy or medical condition requiring long-term anticoagulant therapy (e.g. warfarin) after transplantation (low-dose aspirin treatment is allowed) or subjects with international normalized ratio (INR) > 1.5
  • Severe co-existing cardiac disease
  • Persistent elevation of liver function tests at the time of study entry
  • Acute or chronic pancreatitis
  • Male subjects with elevation of prostate specific antigen
  • Pregnancy
  • Positive screen for polyoma (BK) virus
  • Untreated hyperlipidemia
  • Recent hemorrhagic stroke
  • Factors associated with an increased risk of bleeding

Contact PI for complete Incl-Excl criteria list.

Treatment and study plan

Purified Pancreatic Islets

Biological

Islet after kidney transplant in patients with type I diabetes.

etanercept

Drug

Given as induction for islet cell transplant

Primary outcomes

  1. Insulin Independence With Both an HbA1c ≤ 6.5% and no Severe Hypoglycemic Events at 1 Year After the First Islet Transplant or a Reduction in HbA1c of at Least 1 Point and no Severe Hypoglycemic Events at 1 Year After the First Islet Transplant.

    Time frame: 1 year after the subject's first islet transplant

Secondary outcomes

  1. Number of Participants With a Decrease in HbA1c

    Time frame: 1 year after subject's first islet transplant

    Subjects will have a decrease in HbA1c of at least >1%

  2. Stable or Decrease in Urinary Albumin and Creatinine Ratio and Serum Creatinine

    Time frame: 1 year after subjects initial islet transplant

    Proteinuria and serum creatinine will be stable or decreased as compared to pre-transplant values

  3. An Absence Cardiovascular Events, Cerebral Vascular Accident, and Myocardial Infarction

    Time frame: 1 year after the subject's first islet transplant

  4. Impact on Vision

    Time frame: 1 year after the subject's first islet transplant

    Improvement of frequency of interventions and from changes in reported visual acuity with optical refraction and severity of diabetic retinopathy

  5. Absence of Negative Renal Impact Measures

    Time frame: 1 year after the subject's first islet transplant

    Loss of allograft survivial (return to dialysis, retransplant, death) and Renal allograft function meausred by SCr

  6. Improvement of Metabolic Control

    Time frame: 1 year after the subject's first islet transplant

    Whether there is an improvement in metabolic control in IAK will be evaluated based on improvement in

    • basal c-peptide levels,
    • MMTT,
    • insulin requirements, and
    • c-peptide to glucose, creatinine ratio (CPGCR).
  7. Number of Participants With a Decrease of Severe Hypoglycemic Events

    Time frame: 1 year after subject's first transplant

    Subjects will have a decrease in severe hypoglycemic events

  8. Reduction of Insulin Requriements

    Time frame: 1 year after the subject's first islet transplant

    Evidence of partial success will be considered for subjects who have a reduction in insulin requirements but who are not insulin independent. This will be assessed by comparing the pre-transplant insulin requirement expressed as insulin units per kg per day with the requirement preceding subsequent islet transplants and the insulin requirements at 6 months and 1, 2, and 3 years after the first and last transplant.

Sponsors and collaborators

Lead sponsor

Massachusetts General Hospital

Other

Collaborators

  • Boston Area Diabetes Endocrinology Research Center (funded by NIDDK)

Registry information

Official study title

Islet Transplantation in Type 1 Diabetic Kidney Allograft Recipients

Important dates

Study start
2009
Primary completion
2014
Study completion
2016
First posted
Apr 27, 2009
Registry last updated
Nov 29, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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