Principal Investigator
Enrollment Status
Clinical Trial ID
Clinical Trial Summary
SPECIFIC AIMS:
1. To reverse hyperglycemia and insulin dependency in patients with Type 1 Diabetes
Mellitus by islet cell transplantation;
2. To eliminate the incidence of hypoglycemia coma and unawareness in patients with Type 1
Diabetes Mellitus by islet cell transplantation;
3. To assess long-term safety and function of successful islet cell transplants in patients
with Type 1 Diabetes Mellitus;
4. To determine whether the natural history of the microvascular, macrovascular and
neuropathic complications of Diabetes Mellitus are altered following successful
transplantation of islet cells; and
5. To assess the effect of infliximab in preventing early islet destruction, and thereby
eliminating the need for a second donor's islet cells.
6. To assess the effect of etanercept in preventing early islet destruction.
7. To assess the effect of exenatide to improve islet graft function and survival in
subjects that have returned to using exogenous insulin.
8. To assess the ability of exenatide to improve islet survival at time of transplantation.
Phase
Phase 2
Funding Agency/Sponsor
Other
Disease
Islet Transplant
Enrollment Eligibility
Inclusion Criteria:
1. Patients between 18 and 65 years of age
2. Patients with type 1 diabetes mellitus for more than 5 years duration
3. One or more of the following:
- Hypoglycemia unawareness - judged by history of blood sugars <54 on glucometer
without symptoms and/or hypoglycemic episodes requiring assistance from either
family, glucagon administration or emergency services
- Poor diabetes control (HbA1c>8% or >2 visits/yr to hospital for treatment of
ketoacidosis) despite intensive insulin therapy
- Progressive complications of type 1 diabetes mellitus
4. Body Mass Index (BMI) ≤26
Exclusion Criteria:
1. c-peptide > 0.3ng/ml basal or stimulated;
2. untreated proliferative diabetic retinopathy;
3. HbA1C >12%;
4. creatinine clearance <60;
5. serum creatinine consistently >1.6 mg/dl;
6. macroalbuminuria >300mg albumin in 24 hours;
7. presence of panel reactive antibodies (PRA) >20%;
8. previous/concurrent organ transplantation (except previous unsuccessful islet cell
transplant;
9. malignancy or previous malignancy (except non-melanomatous skin cancer);
10. x-ray evidence of pulmonary infection;
11. active infections;
12. active peptic ulcer disease, gall stones, hemangioma, or portal hypertension
13. serological evidence of HIV, HbsAg or HCV; serological evidence of active EBV
(IgM>IgG) or EBV negative serology;
14. PPD conversion or positive PPD without historic completion of appropriate prophylactic
treatment;
15. abnormal liver function test;
16. anemia (hemoglobin <12.0);
17. hyperlipidemia (fasting serum triglycerides >200mg/dl and/or fasting serum cholesterol
>240 mg/dl and/or fasting LDL cholesterol >140 mg/dl);
18. BMI above 26;
19. unstable cardiovascular status; prostate specific antigen (PSA) >4;
20. pregnancy or breastfeeding;
21. sexually-active females who are not: a) post-menopausal, b) surgically sterile, or c)
not using an acceptable method of contraception (oral contraceptives, Norplant,
Depo-Provera, and barrier devices are acceptable; condoms used alone are not
acceptable);
22. alcohol abuse, substance abuse or smoking within the previous 6 months; insulin
requirement >1u/kg/day and any condition or any circumstance that makes it unsafe to
undergo an islet cell transplant.