An Open Label, Pilot Investigation, to Assess the Safety and Efficacy of Transplantation of Macro-encapsulated Human Islets Within the Bioartificial Pancreas Beta-Air in Patients With Type 1 Diabetes Mellitus

Prior treatment

• Women of childbearing potential who are pregnant, breast-feeding or intend to become pregnant or unwilling to use adequate contraceptive methods for the duration of the trial (implants, injectables, combined oral contraceptives, hormonal intrauterine device, sexual abstinence or vasectomised partner).
• Known active alcohol or drug abuse.
• Administration of live attenuated vaccine(s) within 8 weeks of enrolment
• Any previous organ transplant
• Treatment with any immunosuppressive drug
• The receipt of any investigational product within 30 days of screening for this trial
• Any scheduled transplant in addition to the islet transplantation
• Fulfillment of criteria for clinical pancreas or islet transplantation

Other illness

• Renal failure (Glomerular Filtration Rate \<60 ml/min)
• Active infection including hepatitis B, hepatitis C, HIV, Tbc
• Any history of malignancy except for completely resected squamous or basal cell carcinoma of the skin
• Use of any medications to treat diabetes other than insulin within 4 weeks of enrolment
• Any medical condition that, in the opinion of the investigator, will interfere with safe participation in the trial (e.g., systemic glucocorticoids)
• Known or suspected allergy of hypersensitivity to trial product(s) or related products

Lab values

• HbA1c \> 10 % (DCCT)
• Any coagulopathy or medical condition that would require long-term anticoagulant therapy (e.g., Warfarin) after transplantation (low-dose aspirin treatment is allowed) or subjects with an international normalized ratio (INR) \> 1.5.
• Severe co-existing cardiac disease, characterized by any of these conditions:
  • Recent myocardial infarction (within past 36 weeks)
  • Evidence of ischemia on functional cardiac exam within the last year
  • Left ventricular ejection fraction \< 30 %
  • Cardiovascular conditions within 36 weeks prior to this trial:
  • Decompensated heart failure New York Heart Association (NYHA) class III or IV ii. Unstable angina pectoris iii. Coronary arterial bypass graft iv. Coronary angioplasty

Other

• Body mass index (BMI) \> 30 kg/m²
• Insulin requirement of \> 1.0 Units/kg/day
• Random C-peptide \> 0.003 nmol/l
• Known untreated active proliferative diabetic retinopathy changes or increasing macular oedema
• Inadequately treated blood pressure elevation (systolic BP \> 160 mmHg or diastolic blood pressure \> 100 mmHg)

• Informed consent obtained before any investigation-related activities. Investigation-related activities are any procedure that would not have been performed during normal management of the subject.
• Diagnosis of type 1 diabetes mellitus for \> 5 years
• Men or women \> 18 years of age at the time of enrolment
• Involvement in intensive diabetes management defined as self-monitoring of blood glucose level no less than a mean of three times per day averaged over each week and by the administration of three or more insulin injections per day or insulin pump therapy. This management must be under the direction of a diabetologist or diabetes specialist during the 12 months prior to study enrolment.