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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00888628
Other study ID # IAK
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received April 23, 2009
Last updated October 24, 2017
Start date May 2009
Est. completion date August 2016

Study information

Verified date October 2017
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Description:

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.


Recruitment information / eligibility

Status Completed
Enrollment 7
Est. completion date August 2016
Est. primary completion date August 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility 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.

Study Design


Intervention

Biological:
Purified Pancreatic Islets
Islet after kidney transplant in patients with type I diabetes.
Drug:
Etanercept
Given as induction for islet cell transplant

Locations

Country Name City State
United States Massachusetts General Hospital Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Massachusetts General Hospital Boston Area Diabetes Endocrinology Research Center (funded by NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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. 1 year after the subject's first islet transplant
Secondary Number of Participants With a Decrease in HbA1c Subjects will have a decrease in HbA1c of at least >1% 1 year after subject's first islet transplant
Secondary Stable or Decrease in Urinary Albumin and Creatinine Ratio and Serum Creatinine Proteinuria and serum creatinine will be stable or decreased as compared to pre-transplant values 1 year after subjects initial islet transplant
Secondary An Absence Cardiovascular Events, Cerebral Vascular Accident, and Myocardial Infarction 1 year after the subject's first islet transplant
Secondary Impact on Vision Improvement of frequency of interventions and from changes in reported visual acuity with optical refraction and severity of diabetic retinopathy 1 year after the subject's first islet transplant
Secondary Absence of Negative Renal Impact Measures Loss of allograft survivial (return to dialysis, retransplant, death) and Renal allograft function meausred by SCr 1 year after the subject's first islet transplant
Secondary Improvement of Metabolic Control 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).
1 year after the subject's first islet transplant
Secondary Number of Participants With a Decrease of Severe Hypoglycemic Events Subjects will have a decrease in severe hypoglycemic events 1 year after subject's first transplant
Secondary Reduction of Insulin Requriements 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. 1 year after the subject's first islet transplant
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