Islet Transplantation in Type 1 Diabetic Patients Using the University of Illinois at Chicago (UIC) Protocol

Type 1 Diabetes Mellitus Clinical Trial

Official title:

Islet Transplantation in Type 1 Diabetic Patients Using the UIC Protocol, Phase 3

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT00679042
• Other study ID #: IND11807-2007-0330
• Status: Active, not recruiting
• Phase: Phase 3
• Start date: September 5, 2007
• Est. completion date: June 14, 2026

Study information

• Verified date: August 2023
• Source: CellTrans Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In an earlier Phase 1/2 clinical trial using the Edmonton Protocol of steroid free immunosuppression, investigators at University of Illinois at Chicago (UIC) demonstrated the safety of islet preparation, iset transplantation, and medical treatment at UIC. Therefore, the primary purpose of the present Phase 3 clinical trial is to demonstrate the safety and efficacy of allogeneic islet transplantation in improving glycemic control in Type 1 diabetic patients using the UIC protocol that was developed and proven effective during the Phase 1/2 clinical trial.

Description:

This study is a Phase 3 single center, uncontrolled trial in which 1-3 allogeneic pancreatic islet transplants are performed for each study subject. Follow-up evaluations after transplant continue for 52 weeks after the final islet transplantation. Thereafter, subjects may enroll for a 5-year follow-up study and an additional 5 year to 10 year follow-up study to evaluate the function of the islets and to measure and regulate immunosuppressive drug levels and side effects.

The safety of islet transplantation depends primarily on the incidence of serious and unexpected complications or adverse events and the ability of the cell isolation laboratory to produce uncontaminated islet cell preparations with minimal endotoxin content.

All study subjects are followed for safety for one year. An independent Data Monitoring Committee (DMC), composed of 3 members who have training in medicine and/or organ transplantation, will review eligibility and safety data within 2 weeks after each islet transplantation and every two months thereafter. An independent monitor, who is knowledgeable about Good Clinical Practice (GCP) guidelines and regulations, monitors the study for compliance with 21 CFR and according to ICH GCP Guidelines. Within the Clinical Research Center, representatives of the Scientific Advisory Committee and the Research Subject Advocacy Program monitor safety. These entities report to the UIC Institutional Review Board (IRB), which also reviews safety data annually and on occurrence of serious adverse events. The principal investigator also reports serious adverse events to the US Food and Drug Administration (FDA).

Success: Islet transplantation is considered a success when subjects do not use insulin, and they achieve a fasting glucose level not exceeding 140 mg/dL more than three times in a week, and not exceeding two-hour post-prandial values of 180 mg/dL more than four times in a week.

Partial Success: Subjects who have a reduction in insulin requirements but who do not achieve insulin independence and present with a reduction in HbA1c and number of hypoglycemic episodes are considered to have partial success of islet transplantation. Reduction in insulin-requirements are assessed by comparing the pre-transplant insulin requirement recorded over two consecutive days (expressed as insulin units per kg) with the requirement on the two consecutive days preceding the subsequent islet infusion, and the requirements on two consecutive days at six months and again on two consecutive days at one year after the final transplant.

Failure: Absence of measurable levels of C-peptide after transplantation is considered as failure of islet cell transplantation.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 21
• Est. completion date: June 14, 2026
• Est. primary completion date: July 19, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Type 1 diabetes mellitus for more than 5 years complicated by the following situations that persist despite intensive insulin management efforts:

• At least one episode of severe hypoglycemia in the past 3 years defined as an event with symptoms compatible with hypoglycemia in which the subject required the assistance of another person, and which was associated with either a blood glucose level <50 mg/dL (2.8 mmol/L) or prompt recovery after oral carbohydrate, intravenous glucose, or glucagon administration

• Reduced awareness of hypoglycemia, defined by the absence of adequate autonomic symptoms at capillary glucose levels of <54 mg/dL (3 mmol/l) as reported by the subject

Exclusion Criteria:

• Co-existing cardiac disease: myocardial infarction within the past 6 months, angiographic evidence of non-correctable coronary artery disease, ischemia on functional cardiac exam, heart failure

• Active alcohol or substance abuse, including cigarette smoking (must be abstinent for six months)

• Psychiatric disorder: schizophrenia, bipolar disorder, or major depression that is unstable on medication

• History of non-adherence to prescribed regimens

• Active infection including hepatitis C, hepatitis B, HIV

• TB by history, current infection, or under treatment for suspected TB

• History of malignancies except squamous or basal skin cancer

• Family history of MEN2 or MCT

• Stroke within the past 6 months

• BMI >27 kg/m2

• C-peptide response to glucagon stimulation, any C-peptide >0.3 ng/mL

• Inability to provide informed consent

• Age less than 18 or greater than 75 years

• Creatinine clearance <80 mL/min/1.73 m2 by 24-hour urine collection

• Serum creatinine consistently >1.5 mg/dL

• Macroalbuminuria >300 mg/24h

• Baseline Hb <12 gm/dL in women, <13 gm/dL in men

• Baseline liver function tests outside normal range

• Untreated proliferative retinopathy

• Positive pregnancy test, intent for pregnancy, male's intent to procreate, unwilling to use effective contraception, breast feeding

• Previous transplant or PRA reactivity >80%

• Insulin requirement >0.7 IU/kg/day

• HbA1c >12%

• Hyperlipidemia (fasting cholesterol >130 mg/dL or fasting triglycerides >200 mg/dL

• Medical condition requiring chronic use of steroids

• Use of Coumadin or other antiplatelet or anticoagulant therapy, or PT-INR >1.5

• Factor V deficiency

• Smoking tobacco

• Addison's disease

• Allergy to radiographic contrast material

• Symptomatic cholecystolithiasis

• Acute or chronic pancreatitis

• Symptomatic peptic ulcer disease

• Severe unremitting diarrhea, vomiting, or other gastrointestinal disorders that could interfere with medication absorption

• Treatment with antidiabetic medication other than insulin within 4 weeks of enrollment

• Use of any study medication within 4 weeks of enrollment

• Received live attenuated vaccine(s) within 2 months of enrollment

• Any medical condition that, in the opinion of the investigator, might interfere with safe participation

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Mellitus, Type 1
• Type 1 Diabetes Mellitus

Intervention

Biological:
• Islets of Langerhans transplantation
Each subject may receive 1-3 transplantations of allogeneic human islets of Langerhans and the following medications: Basiliximab 20 mg iv 2 hours before transplant and 20 mg iv 2 weeks post-transplant; Tacrolimus 1 mg p.o. bid adjusted to reach target trough levels of 3-6 ng/ml; Sirolimus 0.2 mg/kg loading dose, then 0.1 mg/kg p.o. daily adjusted to reach target trough levels of 10-15 ng/ml during the first 3 months post transplant and 7-10 ng/ml thereafter; Etanercept 50 mg iv 1 hour before transplant and 25 mg s.c. on days 3, 7,and 10 post-transplant; Exenatide 5-mcg s.c. bid for 1 week, then 10 mcg bid for 6 months after each transplant

Locations

Country	Name	City	State
United States	University of Illinois at Chicago Medical Center	Chicago	Illinois

Sponsors (1)

Lead Sponsor	Collaborator
CellTrans Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Treatment Emergent Adverse Events	Safety endpoints: Incidence and severity of events related to islet infusion, immunosuppression, and islet preparations	From first islet transplant through one year after last transplant (maximum 3 infusions possible), an average of 1 year
Primary	Number of Subjects Reaching the Efficacy Goal	A successful primary endpoint was defined as HbA1c = 6.5% at the one-year follow-up visit and absence of severe hypoglycemic events (SHE) from Day 28 post-first transplant to 1 year after first and last transplant.; The primary analysis was to estimate the true rate of the composite favorable outcome at 1 year following first and last transplant in patients in the ITT population.	One year after islet transplant
Secondary	Number of Patients Presenting With Insulin Independence at Day 365 Post First and Last Transplant	Number of patients presenting with insulin independence, including: Absence of exogenous insulin injection reported at Day 365.; Fasting capillary glucose level not exceeding 140 mg/dL (7.8 mmol/L) more than 3 times in a week (based on measuring capillary glucose levels a minimum of 7 times in a 7-day period) at Day 365 ± 28 days.; Fasting plasma glucose level = 126 mg/dL (7.0 mmol/L) at Day 365 ± 28 days (if the fasting plasma glucose level is > 126 mg/dL [7.0 mmol/L], it must have been confirmed in an additional 1 out of 2 measurements).; Two-hour post-prandial capillary glucose not exceeding 180 mg/dL (10.0 mmol/L) more than 1 out of every 7 times in a week (based on measuring capillary glucose levels a minimum of 7 times in a 7-day period) at Day 365 ± 28 days.; Evidence of endogenous insulin production defined as fasting or stimulated C-peptide levels = 0.5 ng/mL (0.16 nmol/L) at Day 365 ± 28 days	1 year after islet infusion
Secondary	Hypoglycemic Episodes by HYPO Score	Hypoglycemic episodes will be measured by the Ryan hypoglycemic (HYPO) Score derived from the number and severity of hypoglycemic episodes recorded throughout the follow-up phase from Day 28 to Day 365.; (From Ryan et al., 2004) "A HYPO score was generated based on a combination of scores from the 4 weeks of readings and the patients' self-reported episodes over the previous year using the scoring system found in online appendix 2 (available at http://diabetes.diabetesjournals.org). The record sheets returned by the patients were analyzed for the number of episodes of glucose values recorded as <2.5 mmol/l and between 2.5 and 2.9 mmol/l. Points were awarded if symptoms were absent or were neuroglycopenic rather than autonomic... Thus the more severe the problem with hypoglycemia, the higher the score." A Ryan score ranges from 0 (no event) to a cumulative sum of episode points of total events reported during the 4 weeks then multiplied by 13 to provide a 1-year value.	One year after the last transplant
Secondary	Reduction in Hypoglycemic Severity Measured by %Reduction in HYPO Score	%reduction in Ryan HYPO Score [%(baseline score - 1-year post transplant score)/baseline] at time of evaluation.	One year after the first and last transplant

External Links

•   The Chicago Diabetes Project Homepage
•   University of Illinois at Chicago Department of Surgery Homepage