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

Primary Purpose

Diabetes Mellitus, Type 1

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Islet Transplantation
Sponsored by
Rodolfo Alejandro
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 1 focused on measuring Islet Transplantation

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

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 < 11.0 g/dl; females < 10.0 g/dl). Abnormal liver function tests (consistently > 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.

Sites / Locations

  • Diabetes Research Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Islet Transplantation

Arm Description

Islet Transplantation in subjects with a previous kidney transplant.

Outcomes

Primary Outcome Measures

Insulin Independence.
Number of Participants who Achieved Insulin Independence at 1 Year

Secondary Outcome Measures

Stimulated C-peptide Greater Than 0.5 ng/ml
Partial graft function, as evidenced by basal C-peptide greater than 0.5 ng/ml
Reduction of Insulin Requirements
Reduction in insulin requirements in those patients who do not achieve insulin independence
Reduction in Severe Hypoglycemia, Improvement in Hypoglycemia Awareness
Elimination or reduction in the incidence of hypoglycemic coma or unawareness

Full Information

First Posted
April 14, 2006
Last Updated
February 28, 2017
Sponsor
Rodolfo Alejandro
Collaborators
National Institutes of Health (NIH), Health Resources and Services Administration (HRSA), Diabetes Research Institute Foundation, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT00315588
Brief Title
Islet Cell Transplantation in Patients With Type I Diabetes With Previous Kidney Transplantation
Official Title
Islet Cell Transplantation in Patients With Type I Diabetes With Previous Kidney Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
December 2000 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Rodolfo Alejandro
Collaborators
National Institutes of Health (NIH), Health Resources and Services Administration (HRSA), Diabetes Research Institute Foundation, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.
Detailed Description
To reverse hyperglycemia and insulin dependency by islet cell transplantation, in patients with Type 1 Diabetes Mellitus who have a stable kidney allograft; To eliminate the incidence of hypoglycemic coma and unawareness by islet cell transplantation; To assess long-term function of successful islet cell transplants; To determine whether the natural history of the microvascular, macrovascular and neuropathic complications of Diabetes Mellitus are altered following successful transplantation of islet cells. To assess the effect of exenatide to improve islet graft function and survival in subjects that demonstrate partial graft loss and have returned to using exogenous insulin. To assess the ability of exenatide to improve islet survival at time of islet transplantation

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 1
Keywords
Islet Transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
7 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Islet Transplantation
Arm Type
Experimental
Arm Description
Islet Transplantation in subjects with a previous kidney transplant.
Intervention Type
Drug
Intervention Name(s)
Islet Transplantation
Other Intervention Name(s)
islet
Intervention Description
Islet Transplantation in subjects with a previous kidney transplant.
Primary Outcome Measure Information:
Title
Insulin Independence.
Description
Number of Participants who Achieved Insulin Independence at 1 Year
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Stimulated C-peptide Greater Than 0.5 ng/ml
Description
Partial graft function, as evidenced by basal C-peptide greater than 0.5 ng/ml
Time Frame
1 year
Title
Reduction of Insulin Requirements
Description
Reduction in insulin requirements in those patients who do not achieve insulin independence
Time Frame
1year
Title
Reduction in Severe Hypoglycemia, Improvement in Hypoglycemia Awareness
Description
Elimination or reduction in the incidence of hypoglycemic coma or unawareness
Time Frame
1 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
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 < 11.0 g/dl; females < 10.0 g/dl). Abnormal liver function tests (consistently > 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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rodolfo Alejandro, M.D.
Organizational Affiliation
University of Miami
Official's Role
Principal Investigator
Facility Information:
Facility Name
Diabetes Research Institute
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
18360260
Citation
Cure P, Pileggi A, Froud T, Messinger S, Faradji RN, Baidal DA, Cardani R, Curry A, Poggioli R, Pugliese A, Betancourt A, Esquenazi V, Ciancio G, Selvaggi G, Burke GW 3rd, Ricordi C, Alejandro R. Improved metabolic control and quality of life in seven patients with type 1 diabetes following islet after kidney transplantation. Transplantation. 2008 Mar 27;85(6):801-12. doi: 10.1097/TP.0b013e318166a27b.
Results Reference
result
PubMed Identifier
20003758
Citation
Faradji RN, Froud T, Messinger S, Monroy K, Pileggi A, Mineo D, Tharavanij T, Mendez AJ, Ricordi C, Alejandro R. Long-term metabolic and hormonal effects of exenatide on islet transplant recipients with allograft dysfunction. Cell Transplant. 2009;18(10):1247-59. doi: 10.3727/096368909X474456.
Results Reference
derived
PubMed Identifier
19005394
Citation
Tharavanij T, Betancourt A, Messinger S, Cure P, Leitao CB, Baidal DA, Froud T, Ricordi C, Alejandro R. Improved long-term health-related quality of life after islet transplantation. Transplantation. 2008 Nov 15;86(9):1161-7. doi: 10.1097/TP.0b013e31818a7f45.
Results Reference
derived
Links:
URL
http://www.diabetesresearch.org
Description
Research into finding the cure for types 1 and type 2 diabetes.

Learn more about this trial

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

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