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

Primary Purpose

Type 1 Diabetes Mellitus

Status

Active

Phase

Phase 3

Locations

United States

Study Type

Interventional

Intervention

Islets of Langerhans transplantation

About this trial

This is an interventional treatment trial for Type 1 Diabetes Mellitus focused on measuring Diabetes Mellitus Type 1, Type 1 Diabetes Mellitus, Islets of Langerhans Transplantation, Allogeneic Islet transplantation

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

University of Illinois at Chicago Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Treatment

Arm Description

All subjects will receive up to 3 transplantations of allogeneic human islets of Langerhans.

Outcomes

Primary Outcome Measures

Treatment Emergent Adverse Events

Safety endpoints: Incidence and severity of events related to islet infusion, immunosuppression, and islet preparations

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.

Secondary Outcome Measures

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

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.

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.

Full Information

NCT ID

NCT00679042

First Posted

May 13, 2008

Last Updated

August 28, 2023

Sponsor

CellTrans Inc.

1. Study Identification

Unique Protocol Identification Number

NCT00679042

Brief Title

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

Official Title

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

Study Type

Interventional

2. Study Status

Record Verification Date

August 2023

Overall Recruitment Status

Active, not recruiting

Study Start Date

September 5, 2007 (Actual)

Primary Completion Date

July 19, 2017 (Actual)

Study Completion Date

June 14, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Principal Investigator

Name of the Sponsor

CellTrans Inc.

4. Oversight

Data Monitoring Committee

Yes

5. Study Description

Brief 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.

Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Type 1 Diabetes Mellitus

Keywords

Diabetes Mellitus Type 1, Type 1 Diabetes Mellitus, Islets of Langerhans Transplantation, Allogeneic Islet transplantation

7. Study Design

Primary Purpose

Treatment

Study Phase

Phase 3

Interventional Study Model

Single Group Assignment

Masking

None (Open Label)

Allocation

N/A

Enrollment

21 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Treatment

Arm Type

Experimental

Arm Description

All subjects will receive up to 3 transplantations of allogeneic human islets of Langerhans.

Intervention Type

Biological

Intervention Name(s)

Islets of Langerhans transplantation

Other Intervention Name(s)

Islets of Langerhan (Islets), Basiliximab (Simulect®), Tacrolimus (Prograf®), Sirolimus (Rapamune®), Etanercept(Enbrel®), Exenatide (Byetta®)

Intervention Description

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

Primary Outcome Measure Information:

Title

Treatment Emergent Adverse Events

Description

Safety endpoints: Incidence and severity of events related to islet infusion, immunosuppression, and islet preparations

Time Frame

From first islet transplant through one year after last transplant (maximum 3 infusions possible), an average of 1 year

Title

Number of Subjects Reaching the Efficacy Goal

Description

Time Frame

One year after islet transplant

Secondary Outcome Measure Information:

Title

Number of Patients Presenting With Insulin Independence at Day 365 Post First and Last Transplant

Description

Time Frame

1 year after islet infusion

Title

Hypoglycemic Episodes by HYPO Score

Description

Time Frame

One year after the last transplant

Title

Reduction in Hypoglycemic Severity Measured by %Reduction in HYPO Score

Description

%reduction in Ryan HYPO Score [%(baseline score - 1-year post transplant score)/baseline] at time of evaluation.

Time Frame

One year after the first and last transplant

10. Eligibility

Sex

All

Minimum Age & Unit of Time

18 Years

Maximum Age & Unit of Time

75 Years

Accepts Healthy Volunteers

Eligibility Criteria

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

Overall Study Officials:

First Name & Middle Initial & Last Name & Degree

Jose Oberholzer, MD

Organizational Affiliation

University of Illinois at Chicago

Official's Role

Principal Investigator

Facility Information:

Facility Name

University of Illinois at Chicago Medical Center

City

Chicago

State/Province

Illinois

ZIP/Postal Code

60612

Country

United States

12. IPD Sharing Statement

Plan to Share IPD

Citations:

PubMed Identifier

29779835

Citation

Luu QF, Villareal CJ, Fritschi C, Monson RS, Oberholzer J, Danielson KK. Concerns and hopes of patients with type 1 diabetes prior to islet cell transplantation: A content analysis. J Diabetes Complications. 2018 Jul;32(7):677-681. doi: 10.1016/j.jdiacomp.2018.04.002. Epub 2018 Apr 17.

Results Reference

derived

Links:

URL

http://www.uic.edu/com/surgery/transplant/research.htm

Description

University of Illinois at Chicago Department of Surgery Homepage

URL

http://chicagodiabetesproject.org

Description

The Chicago Diabetes Project Homepage

Learn more about this trial

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

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