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

Phase 1

Active, not recruiting

• Conditions: Long-standing Type 1 Diabetes Mellitus
• Interventions: Device: Beta-Air device for encapsulation of transplanted human islets

• Registration Number: NCT02064309
• Lead Sponsor: Uppsala University Hospital

Brief Summary

The primary objective of this clinical investigation is to investigate the safety of implantation of the human islet containing device Beta-Air in type 1 diabetic subjects.

The secondary objective of this clinical investigation is to investigate if the transplantation of macro-encapsulated human islets within the Beta-Air device can provide improved glycaemic control in type 1 diabetes patients with reduced incidences of hypoglycaemic episodes.

Detailed Description

Not available

Study Timeline

• Study Start: 2014-02
• Study First Submitted: 2014-02-13
• Study First Submitted QC: 2014-02-13
• Study First Posted: 2014-02-17
• Status Verified: 2024-12
• Last Update Submitted: 2024-12-04
• Last Update Posted: 2024-12-05
• Primary Completion: 2025-05
• Study Completion: 2025-05

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 4

Inclusion Criteria

1. 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.
2. Diagnosis of type 1 diabetes mellitus for > 5 years
3. Men or women > 18 years of age at the time of enrolment
4. 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.

Exclusion Criteria

1. Body mass index (BMI) > 30 kg/m²

2. Insulin requirement of > 1.0 Units/kg/day

3. HbA1c > 10 % (DCCT)

4. Random C-peptide > 0.003 nmol/l

5. Known untreated active proliferative diabetic retinopathy changes or increasing macular oedema

6. Renal failure (Glomerular Filtration Rate <60 ml/min)

7. 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).

8. Active infection including hepatitis B, hepatitis C, HIV, Tbc

9. Any history of malignancy except for completely resected squamous or basal cell carcinoma of the skin

10. Known active alcohol or drug abuse.

11. 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.

12. Severe co-existing cardiac disease, characterized by any of these conditions:

    1. Recent myocardial infarction (within past 36 weeks)
    2. Evidence of ischemia on functional cardiac exam within the last year
    3. Left ventricular ejection fraction < 30 %
    4. Cardiovascular conditions within 36 weeks prior to this trial:

    i. Decompensated heart failure New York Heart Association (NYHA) class III or IV ii. Unstable angina pectoris iii. Coronary arterial bypass graft iv. Coronary angioplasty

13. Inadequately treated blood pressure elevation (systolic BP > 160 mmHg or diastolic blood pressure > 100 mmHg)

14. Use of any medications to treat diabetes other than insulin within 4 weeks of enrolment

15. Administration of live attenuated vaccine(s) within 8 weeks of enrolment

16. Any previous organ transplant

17. Treatment with any immunosuppressive drug

18. Any medical condition that, in the opinion of the investigator, will interfere with safe participation in the trial (e.g., systemic glucocorticoids)

19. Known or suspected allergy of hypersensitivity to trial product(s) or related products

20. The receipt of any investigational product within 30 days of screening for this trial

21. Any scheduled transplant in addition to the islet transplantation

22. Fulfillment of criteria for clinical pancreas or islet transplantation

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Human islets in Beta-Air device	Beta-Air device for encapsulation of transplanted human islets	-

Primary Outcome Measures

Name	Time	Method
Safety of device, as evaluated by incidence of adverse events or serious adverse events judged probable or highly probable related to the device	0-365 days

Secondary Outcome Measures

Name	Time	Method
2. Incidence and severity of fibrosis surrounding the device during course of study.	0-365 days
3. Signs of immunization in transplanted patients.	0-365 days
6. Numbers of patients with peak c-peptide >0.20 nmol/l, in response to the mixed meal tolerance test at 12 and 26 weeks post-transplantation	12 and 26 weeks post-transplantation
1. Incidence of local or systemic inflammation or infection, incl. C-reactive protein rise, judged related to the device during course of study.	0-365 days
7. C-peptide area under the curve in response to the mixed meal tolerance test at 12 and 26 weeks post-transplantation.	12 and 26 weeks post-transplantation
5. Survival of endocrine tissue in the device, as evaluated by [11C]-5-hydroxytryptophane positron emission tomography and histological analysis at 26 weeks post-transplantation.	0-180 days
8. Number of patients with non-fasting c-peptide concentrations >0.003 nmol/l at 1, 2, 3, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24 and 26 weeks post-transplantation; i.e. Kaplan-Meier analysis of survival time for islet grafts.	0-26 weeks
4. Oxygenation of tissue in the device, as evaluated at 4, 12 and 26 weeks post-transplantation	0-180 days

Trial Locations

Locations (1)

Uppsala University Hospital; 🇸🇪 Uppsala, Sweden