Safety and Efficacy of PEG-Encapsulated Islet Allografts Implanted in Type I Diabetic Recipients

Diabetes Mellitus, Type 1 Clinical Trial

Official title:

A Single-Center Phase I/II Study Of Peg-Encapsulated Islet Allografts Implanted In Patients With Type I Diabetes

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00260234
• Other study ID #: NC-PCIA-04-001
• Secondary ID: WIRB #20041068
• Status: Terminated
• Phase: Phase 1/Phase 2
• First received: November 28, 2005
• Last updated: September 8, 2014
• Start date: November 2005
• Est. completion date: December 2007

Study information

• Verified date: September 2014
• Source: Novocell
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Insulin dependent Type I diabetics require daily insulin therapy to normalize blood glucose but may have difficulty with significant glycemic excursions and hypoglycemic episodes and crises. Islet cell transplantation can provide relief from daily insulin therapy, normalize blood glucose and reduce or eliminate short and long-term diabetes-related complications. "PEG-Encapsulated Islet Allografts" is a new islet transplant product under development that does not require the ongoing use of immunosuppressive drugs after the implant. This study will test the safety and efficacy of PEG-Encapsulated Islet Allografts in the treatment of Type I diabetes and provide functional outcome measurements.

Description:

Allogeneic Cultured Islet Cells (human, Novocell); Encapsulated in Polyethylene Glycol; Administered Subcutaneously are a combination biologic and device product in which the pharmacologically active agent is human insulin that is released from the functional islet cells by natural production and release, stimulated by control mechanisms in response to blood glucose concentrations. The device component is a uniform and conformal polymer coating around each islet. Islet cells are isolated from multiple human pancreases procured from human organ donors who meet a specific human donor profile established by the UNOS and the FDA's requirements for Good Tissue Practices. Because the pancreases used for islet cell isolation are not intended for whole-organ transplantation, specific procurement, surgical removal, packaging and shipping protocols are provided by Novocell, Inc. to the Organ Procurement Organizations.

The primary outcome is demonstration that encapsulated islet allografts can be implanted safely in the subcutaneous tissues without the use of long-term immunosuppression. The expected functional outcomes from the implantation of the encapsulated islets are significant reductions in the average blood glucose daily glycemic excursions and in insulin requirements as well as significant increases in C-peptide levels in response to meal challenges. The ultimate expected outcome is that patients who receive these implants will have reduced hemoglobin A1c levels that may be associated with reduced long-term diabetic complications. An important outcome should be reduction in hypoglycemic episodes and crises with significantly functioning grafts without having the risks associated with hepatic portal vein infusion and long-term immunosuppression.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 12
• Est. completion date: December 2007
• Est. primary completion date: December 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years and older

Eligibility

Inclusion Criteria:

• Male or non-pregnant non-lactating female subjects > 20 years of age

• Diagnosed with insulin-dependent type I diabetes for at least 20 years

• BMI less than 28 kg/m2

• Insulin requirement less than or equal to 0.7 U/kg/day

• HbA1c greater than or equal to 7.0 %

• Serum C-peptide concentration less than or equal to 0.5 ng/mL stimulated by an OGTT

• Female subjects with childbearing potential must have a negative serum pregnancy test prior to enrollment and must agree to use an effective contraceptive method during the study

• One year of stable diabetes care established in the PI's database without significant changes in insulin requirement or HbA1c or diabetic complication profile

Exclusion Criteria:

• Diagnosis of type II diabetes or maturity onset diabetes of youth (MODY)

• Serum C-peptide greater than 0.5 ng/mL stimulated by OGTT

• Sustained hypertension greater than or equal to 100 mmHg diastolic and/or greater than or equal to 160 mmHg systolic

• History of myocardial infarction or current active cardiac disease

• Current active infection

• Significant renal dysfunction as indicated by GFR less than 80 mL/min/1.73 m2 and/or urinary albumin greater than 500 µg/mL

• Significant liver dysfunction as indicated by ALT or AST more than 3X the upper limit of normal

• Prior whole organ or islet cell transplant

• Concurrent immunosuppressive therapy

• Severe gastroparesis, severe peripheral neuropathy, diabetic foot ulcers, or prior amputations due to diabetic complications

• Any other active autoimmune disease other than autoimmune thyroid disease

• HIV, HBV or HCV positive status

• Uncontrolled or untreated proliferative retinopathy

• Known hypersensitivity or other intolerance to cyclosporine or the inactive ingredients in the product

• Behavioral activities that place the subject at risk in the opinion of the investigator

• Any significant concurrent disease, illness, or psychiatric disorder that would, in the opinion of the investigator, compromise subject safety or compliance, or interfere with consent, study participation, follow-up, or the interpretation of study results

• History of any kind of cancer other than skin cancers (except for melanoma which is exclusionary)

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Mellitus, Type 1

Intervention

Biological:
• Allogeneic Cultured Islet Cells (human); Encapsulated

Locations

Country	Name	City	State
United States	CHRISTUS Santa Rosa Transplant Institute	San Antonio	Texas
United States	Diabetes & Glandular Disease Research Associates, P.A.	San Antonio	Texas

Sponsors (3)

Lead Sponsor	Collaborator
Novocell	CHRISTUS Health, Diabetes & Glandular Disease Research Associates, P.A., San Antonio, TX

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety - will be evaluated by the incidence, grade, and type of adverse events, changes in laboratory parameters, evaluation of the implant site and physical exams.
Secondary	Efficacy - will be assessed by:
Secondary	Blood glucose levels
Secondary	Daily glycemic excursions
Secondary	Pre-prandial glucose levels
Secondary	Post-prandial glucose levels
Secondary	Glucose responses from OGTT (mg/dL and AUC:glucose
Secondary	Stimulated C-peptide levels from OGTT (ng/mL and
Secondary	AUC:C-Peptide
Secondary	HbA1c (%)
Secondary	Insulin requirements (units/day)
Secondary	Arginine stimulation tests
Secondary	Numbers of hypoglycemic and hyperglycemic episodes
Secondary	Functional duration - will be determined by stimulated C-peptide from OGTT.

External Links

•   CHRISTUS Santa Rosa website
•   Diabetes & Glandular Disease Research Associates website
•   Sponsor's website