Alemtuzumab Induction in Islet Transplantation

University of Alberta

Status and phase

Completed

Phase 2

Conditions

Type 1 Diabetes

Treatments

Procedure: islet transplant

Drug: alemtuzumab

Study type

Interventional

Funder types

Other

Identifiers

NCT00175253

5369

Details and patient eligibility

About

Our experience suggests that further research with alemtuzumab is attractive in islet transplantation. Therefore, in this study we propose to combine alemtuzumab induction pre-transplant, with tacrolimus and mycophenolate mofetil maintenance immunosuppression post-transplant. In the critical early phase post transplant, we anticipate that this regimen will prove to be more effective in control of autoimmunity or rejection events, and have a more desirable side-effect profile, than previously tested combinations of induction and immunosuppressive agents.

Full description

This trial is a single-center, prospective, open-label study in 12 Type 1 diabetic participants receiving an islet-alone transplant along with alemtuzumab induction therapy followed by combination tacrolimus and MMF maintenance immunosuppression. Participants will receive 1 to 3 infusions of pancreatic islets of sufficient quantity to attain insulin independence.

The primary objective of this protocol is to assess the safety of a treatment regimen utilizing alemtuzumab induction and a combination of tacrolimus and MMF maintenance immunosuppression in adult Type 1 diabetic participants receiving their first islet transplant.

Enrollment

12 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

open to Canadians only
participant must have had Type 1 diabetes mellitus for more than 5 years
diabetes must be complicated by at least 1 of the following situations that persist despite intensive insulin management efforts: (1) Reduced awareness of hypoglycemia, as defined by the absence of adequate autonomic symptoms at plasma glucose levels < 3.0 mmol/L, indicated by, 2 or more episodes of severe hypoglycemia requiring third party assistance within 12 months; or (2) Metabolic instability, characterized by erratic blood glucose levels that interfere with daily activities and or 2 or more hospital visits for diabetic ketoacidosis over the last 12 months.
Participants must be capable of understanding the purpose and risks of the study and must sign a statement of informed consent.

Exclusion criteria

Severe co-existing cardiac disease
Active alcohol or substance abuse, to include cigarette smoking
Psychiatric disorder making the subject not a suitable candidate for transplantation
History of non-adherence to prescribed regimens
Active infection including Hepatitis C, Hepatitis B, HIV, TB
Any history of or current malignancies except squamous or basal skin cancer
BMI > 28 kg/m2 at screening visit
Creatinine clearance < 65 mL/min/1.73 m2
Blood creatinine > 150 µmol/L (1.7 mg/dL)
Macroalbuminuria (urinary albumin excretion rate > 300 mg/24h)
Baseline Hb < 105g/L (<10.5 g/dL) in women, or < 130 g/L (<13 g/dL) in men
Baseline screening liver function tests outside of normal range
Untreated proliferative retinopathy
Positive pregnancy test, intent for future pregnancy or male subjects' intent to procreate, failure to follow effective contraceptive measures, or presently breast feeding
Previous transplant, or evidence of significant sensitization on PRA
Insulin requirement >1.0 U/kg/day
HbA1C >12%
Uncontrolled hyperlipidemia
Under treatment for a medical condition requiring chronic use of steroids
Use of coumadin or other anticoagulant therapy (except aspirin) or subject with PT INR > 1.5
Untreated Celiac disease
Patients with Graves disease will be excluded unless previously adequately treated with radioiodine ablative therapy