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

University of Minnesota (UMN)

Status and phase

Completed

Phase 2

Phase 1

Conditions

Hypoglycemia

Type 1 Diabetes Mellitus

Treatments

Drug: Everolimus

Biological: Allogeneic Islets of Langerhans

Drug: Cyclosporine

Drug: anti-thymocyte globulin

Study type

Interventional

Funder types

Other

Industry

NIH

Identifiers

NCT00286624

0207M29841

Details and patient eligibility

About

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.

Full 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.

Enrollment

6 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No 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.