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Anti-Thymocyte Globulin, Cyclosporine, and RAD in Islet Transplantation (NITA)

Primary Purpose

Type 1 Diabetes Mellitus, Hypoglycemia

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Allogeneic Islets of Langerhans
Everolimus
anti-thymocyte globulin
Cyclosporine
Sponsored by
University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes Mellitus

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Primary islet allotransplant Patients with type 1 diabetes mellitus under intensive insulin management Age 18 or older Ability to give written informed consent Exclusion Criteria: Age less than 18 years. BMI >26 kg/m2. Insulin requirement of > 50 IU per day. Positive C-peptide response to intravenous arginine stimulation. Untreated proliferative retinopathy. Creatinine clearance < 60 ml/min/1.73 m2 for females and 70 ml/min/1.73 m2 for males. Serum creatinine >1.3 mg/dl for females, >1.5 mg/dl for males. Previous pancreas or islet transplant. Presence of history of panel-reactive anti-HLA antibodies >10%. Positive pregnancy test, or presently breast-feeding, or failure to follow effective contraceptive measures. Active infection including hepatitis C, hepatitis B, HIV, or TB (or under treatment for suspected TB). Negative screen for Epstein-Barr Virus (EBV). Invasive aspergillus infection within year prior to study entry. History of malignancy. Active alcohol or substance abuse History of non-adherence to prescribed regimens. Psychiatric disorder making the subject not a suitable candidate for transplantation. Inability to provide informed consent. Baseline Hgb < 11.7 g/dl in females, or < 13 g/dl in males; lymphopenia (<1,000/microL), or leukopenia (<3,000 total leukocytes/microL), or an absolute CD4+ count <500/microL., or platelets <150,000/microL History of coagulopathy or medical condition requiring long-term anticoagulant therapy after transplantation or patient with INR >1.5. Severe co-existing cardiac disease. Baseline liver function tests outside of normal range or history of significant liver disease. Active peptic ulcer disease. Severe unremitting diarrhea or other gastrointestinal disorders potentially interfering with the ability to absorb oral medications. Presence of severe allergy requiring acute or chronic treatment, or hypersensitivity to drugs similar to RAD (e.g., macrolides). Known hypersensitivity to rabbit proteins. Hyperlipidemia (fasting LDL cholesterol > 130 mg/dl, treated or untreated; and/or fasting triglycerides > 200 mg/dl). Addison's disease. Under treatment requiring chronic use of systemic steroids. Any medical condition that, in the opinion of the investigator, will interfere with the safe completion of the trial.

Sites / Locations

  • University of Minnesota

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

Allogeneic islet transplantation with anti-thymocyte globulin induction and cyclosporine and RAD maintenance immunosuppression

Outcomes

Primary Outcome Measures

• The incidence, timing, and severity of adverse events during one year after the first and any subsequent islet transplants.
• Incidence and severity of hypoglycemia during the first year after the first and any subsequent islet transplants.
• The proportion of recipients who develop alloantibodies directed at islet donor alloantigens during the first year after the first and any subsequent islet transplants.

Secondary Outcome Measures

• The proportion of subjects who achieve insulin independence in the first year after single-donor or sequential transplantation.
• The proportion of islet allograft recipients with full and partial islet graft function at one year after the most recent islet transplant.
• Glycemic control and insulin secretory responses during the first year after the first and any subsequent transplants.
• The effect of donor age, pretransplant islet insulin secretory response in vitro, number of transplanted islet equivalents (IEQ), number of transplanted beta cells, pretransplant recipient insulin requirements and action, recipient body mass index (BM
• The impact of islet transplantation on the quality of life of transplant recipients.

Full Information

First Posted
February 2, 2006
Last Updated
May 2, 2008
Sponsor
University of Minnesota
Collaborators
Juvenile Diabetes Research Foundation, National Institutes of Health (NIH), Novartis
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1. Study Identification

Unique Protocol Identification Number
NCT00286624
Brief Title
Anti-Thymocyte Globulin, Cyclosporine, and RAD in Islet Transplantation
Acronym
NITA
Official Title
A One-Year, Single-Center, Prospective, Open-Label Study of the Safety, Tolerability, and Preliminary Efficacy of Anti-Thymocyte Globulin, Cyclosporine, and RAD in Type 1 Diabetic Islet Transplant Recipients
Study Type
Interventional

2. Study Status

Record Verification Date
May 2008
Overall Recruitment Status
Completed
Study Start Date
March 2003 (undefined)
Primary Completion Date
August 2006 (Actual)
Study Completion Date
August 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Minnesota
Collaborators
Juvenile Diabetes Research Foundation, National Institutes of Health (NIH), Novartis

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study was designed to test the safety and efficacy of up to 3 pancreatic alloislet transplants in type 1 diabetic patients with hypoglycemia unawareness. 6 subjects were transplanted under this protocol using anti-thymocyte globulin induction immunosuppression and everolimus with cyclosporine maintenance immunosuppression.
Detailed Description
This is a Phase I/II study designed to assess the safety and efficacy of sequential islet allotransplantation for the reestablishment of stable glycemic control in type 1 diabetic recipients. A total of 6 patients with type 1 diabetes have received up to three transplants of islets from different donor pancreases. Potential candidates for islet allotransplantation included patients age 18 and older with type 1 diabetes. Induction immunotherapy for the first transplant consisted of anti-thymocyte globulin; basiliximab was used for any subsequent transplants. Peritransplant anti-inflammatory treatment with etanercept was given for each islet transplant. Maintenance immunosuppression is with cyclosporine and RAD. It is felt that those patients in whom metabolic lability/instability, reduced awareness of hypoglycemia, poor glycemic control, and progressive secondary complications persist despite continued and intensive efforts made in close cooperation with their diabetes care team are particularly likely to have a favorable benefit/risk ratio. Adverse events, irrespective of their presumed relationship to the transplantation of allogeneic islets and/or protocol-regulated treatment products (concomitant therapy), are being monitored and recorded throughout the first year after the final islet transplant. The proportion of single and sequential donor islet allograft recipients with full (insulin independence and HbA1c <7%) and partial (insulin dependence, basal or arginine-stimulated C-peptide levels of greater or equal to 0.5 ng/mL and HbA1c <7%) islet graft function at one year after the final islet transplant will be assessed. The impact of islet transplantation on quality of life will also be assessed. The predictive value for posttransplant insulin independence of factors such as insulin resistance before and at intervals after pancreatectomy, cellular composition of the transplant, number of beta cells transplanted; and viability and insulin secretory response of isolated islets are being assessed.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
6 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Allogeneic islet transplantation with anti-thymocyte globulin induction and cyclosporine and RAD maintenance immunosuppression
Intervention Type
Biological
Intervention Name(s)
Allogeneic Islets of Langerhans
Other Intervention Name(s)
Islets
Intervention Description
Up to 3 intraportal infusions of cadaveric pancreatic islets of Langerhans. First infusion to contain at least 5,000 islet equivalents/kg body weight. Subsequent infusions to contain at least 3,000 islet equivalents/kg body weight.
Intervention Type
Drug
Intervention Name(s)
Everolimus
Other Intervention Name(s)
RAD
Intervention Description
Loading dose of 3 mg PO on day -2 relative to transplant, followed at least 12 hours later by dose of 1.5 mg PO BID. The daily dose will be adjusted according to the whole blood 12-hr trough to target 3-15 ng/ml for the first 3 months and 3-12 ng/ml thereafter.
Intervention Type
Drug
Intervention Name(s)
anti-thymocyte globulin
Other Intervention Name(s)
ATG, Thymogloblin
Intervention Description
A total of 6 mg/kg IV over 12 hours on days -2, -1, 0, +1, and +2. The dose will be 0.5 mg/kg on day -2, 1.0 mg/kg on day -1, and 1.5 mg/kg on days 0, +1, and +2.
Intervention Type
Drug
Intervention Name(s)
Cyclosporine
Other Intervention Name(s)
Neoral
Intervention Description
Cyclosporine started on day +1 relative to the first islet transplant. Initial dose of 3 mg/kg/day administered in 2 divided doses; then adjusted to maintain target levels of 400 (350-500) ng/mL for the first three months following islet transplant and 300 (200-350) ng/mL thereafter.
Primary Outcome Measure Information:
Title
• The incidence, timing, and severity of adverse events during one year after the first and any subsequent islet transplants.
Time Frame
1 year
Title
• Incidence and severity of hypoglycemia during the first year after the first and any subsequent islet transplants.
Time Frame
1 yr
Title
• The proportion of recipients who develop alloantibodies directed at islet donor alloantigens during the first year after the first and any subsequent islet transplants.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
• The proportion of subjects who achieve insulin independence in the first year after single-donor or sequential transplantation.
Time Frame
1 year
Title
• The proportion of islet allograft recipients with full and partial islet graft function at one year after the most recent islet transplant.
Time Frame
1 year
Title
• Glycemic control and insulin secretory responses during the first year after the first and any subsequent transplants.
Time Frame
1 year
Title
• The effect of donor age, pretransplant islet insulin secretory response in vitro, number of transplanted islet equivalents (IEQ), number of transplanted beta cells, pretransplant recipient insulin requirements and action, recipient body mass index (BM
Time Frame
Day of transplant
Title
• The impact of islet transplantation on the quality of life of transplant recipients.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary islet allotransplant Patients with type 1 diabetes mellitus under intensive insulin management Age 18 or older Ability to give written informed consent Exclusion Criteria: Age less than 18 years. BMI >26 kg/m2. Insulin requirement of > 50 IU per day. Positive C-peptide response to intravenous arginine stimulation. Untreated proliferative retinopathy. Creatinine clearance < 60 ml/min/1.73 m2 for females and 70 ml/min/1.73 m2 for males. Serum creatinine >1.3 mg/dl for females, >1.5 mg/dl for males. Previous pancreas or islet transplant. Presence of history of panel-reactive anti-HLA antibodies >10%. Positive pregnancy test, or presently breast-feeding, or failure to follow effective contraceptive measures. Active infection including hepatitis C, hepatitis B, HIV, or TB (or under treatment for suspected TB). Negative screen for Epstein-Barr Virus (EBV). Invasive aspergillus infection within year prior to study entry. History of malignancy. Active alcohol or substance abuse History of non-adherence to prescribed regimens. Psychiatric disorder making the subject not a suitable candidate for transplantation. Inability to provide informed consent. Baseline Hgb < 11.7 g/dl in females, or < 13 g/dl in males; lymphopenia (<1,000/microL), or leukopenia (<3,000 total leukocytes/microL), or an absolute CD4+ count <500/microL., or platelets <150,000/microL History of coagulopathy or medical condition requiring long-term anticoagulant therapy after transplantation or patient with INR >1.5. Severe co-existing cardiac disease. Baseline liver function tests outside of normal range or history of significant liver disease. Active peptic ulcer disease. Severe unremitting diarrhea or other gastrointestinal disorders potentially interfering with the ability to absorb oral medications. Presence of severe allergy requiring acute or chronic treatment, or hypersensitivity to drugs similar to RAD (e.g., macrolides). Known hypersensitivity to rabbit proteins. Hyperlipidemia (fasting LDL cholesterol > 130 mg/dl, treated or untreated; and/or fasting triglycerides > 200 mg/dl). Addison's disease. Under treatment requiring chronic use of systemic steroids. Any medical condition that, in the opinion of the investigator, will interfere with the safe completion of the trial.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bernhard J. Hering, M.D.
Organizational Affiliation
University of Minnesota
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.diabetesinstitute.org
Description
Diabetes Institute for Immunology and Transplantation - U of M

Learn more about this trial

Anti-Thymocyte Globulin, Cyclosporine, and RAD in Islet Transplantation

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