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Islet Transplant for Type 1 or Surgical Diabetes (EXAX)

Primary Purpose

Type 1 Diabetes Mellitus, Hypoglycemia, Labile Diabetes

Status
Available
Phase
Locations
United States
Study Type
Expanded Access
Intervention
Allogeneic islets of Langerhans
Sponsored by
University of Minnesota
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an expanded access trial for Type 1 Diabetes Mellitus focused on measuring Islet transplant, Diabetes Mellitus, Hypoglycemia

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All Sexes

Inclusion Criteria:

  1. Male and female patients age 18 to 70 years of age.
  2. Ability to provide written informed consent.
  3. Mentally stable and able to comply with the procedures of the study protocol.
  4. Insulin-dependent diabetes mellitus
  5. Not otherwise eligible for an existing alloislet transplant protocol for type 1 diabetes mellitus
  6. Involvement in intensive diabetes management, defined by at least 3 injections daily or insulin pump therapy.
  7. Meets at least one of the following criteria despite intensive efforts made in close cooperation with their diabetic care team:

    • Significant hypoglycemia unawareness or glycemic lability on conventional insulin therapy, as evidenced by at least one of the following at screening:
    • Clarke score > 4
    • HYPO score >90th percentile (1047)
    • Lability index (LI) >90th percentile (433 mM2/h/wk)
    • A composite of a Clarke score of 4 or more and a HYPO score greater than or equal to the 75th percentile (423) and a LI greater than of equal to the 75th percentile (329)
    • Progressive secondary complications as defined by end-stage renal disease necessitating dialysis or renal transplantation (eligible for islet after kidney or simultaneous islet kidney transplant) AND islet transplant appears to provide a more satisfactory benefit to risk ratio compared to pancreas transplantation (eg high surgical risk)

Exclusion Criteria:

  1. HbA1c >10%.
  2. Untreated proliferative diabetic retinopathy.
  3. Uncontrolled Hypertension (SBP>160 or DBP>100)
  4. For female participants: Positive pregnancy test, presently breast-feeding, or unwillingness to use effective contraceptive measures for the duration of the study.
  5. Active infection including hepatitis B, hepatitis C, HIV, or TB as determined by a positive skin test or clinical presentation, or under treatment for suspected TB.
  6. Any history of malignancy except for completely resected squamous or basal cell carcinoma of the skin.
  7. Receiving treatment for a medical condition requiring chronic use of systemic steroids, except for use of prednisone <5 mg per day for kidney transplant recipients or physiologic hydrocortisone replacement.
  8. Persistent elevation of liver function tests at the time of study entry. Persistent SGOT (AST), SGPT (ALT), Alk Phos or total bilirubin, with values >1.5 times normal upper limits will exclude a patient.
  9. Severe co-existing cardiac disease, characterized by any one of these conditions:

    • recent myocardial infarction (within past 6 months).
    • evidence of ischemia on functional cardiac exam within the last year.
    • left ventricular ejection fraction <30%.
  10. If diabetes is secondary to total pancreatectomy, participants will be considered only if >1 year out from surgery, medically stable, without severe issues with bowel function or pain management that may interfere with safe completion of the trial.
  11. History of alcoholism
  12. Any medical condition that, in the opinion of the investigator, will interfere with the safe completion of the trial.

Sites / Locations

  • University of Minnesota

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
May 23, 2012
Last Updated
August 2, 2023
Sponsor
University of Minnesota
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1. Study Identification

Unique Protocol Identification Number
NCT01606475
Brief Title
Islet Transplant for Type 1 or Surgical Diabetes
Acronym
EXAX
Official Title
Human Alloislet Transplant for Type 1 or Surgical Diabetes Mellitus With Complications
Study Type
Expanded Access

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Available
Study Start Date
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Primary Completion Date
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Study Completion Date
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3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to evaluate the safety and efficacy of islet transplants from human cadaver donors into type 1 or surgical diabetes mellitus patients who experience frequent acute or advanced chronic complications but do not qualify for other islet transplant trials. Under this protocol, patients may receive intraportal alloislet transplant under one of the following scenarios: islet transplant alone simultaneous islet-kidney transplant, or 3)islet after kidney transplant.
Detailed Description
The overall objective of this study is to evaluate the efficacy of islet allotransplants for labile diabetes mellitus in patients who do not meet standard inclusion/exclusion criteria for any other islet transplant trials in the US and are not good candidates for a pancreas transplant. We expect that this will include patients who have surgical diabetes (total pancreatectomy) rather than type 1 diabetes, patients who are highly sensitized (PRA>20%), and patients who have had prior failed pancreas transplantation. These patients may have equally severe hypoglycemia, glucose lability, and/or severe microvascular complications, but are excluded from standard islet transplant trials currently available in the U.S.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes Mellitus, Hypoglycemia, Labile Diabetes, End-stage Renal Disease
Keywords
Islet transplant, Diabetes Mellitus, Hypoglycemia

7. Study Design

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
Allogeneic islets of Langerhans
Other Intervention Name(s)
Islets
Intervention Description
Up to 3 intraportal infusions of cadaveric pancreatic islets of Langerhans. Each infusion to contain at least 5,000 islet equivalents/kg body weight.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Eligibility Criteria
Inclusion Criteria: Male and female patients age 18 to 70 years of age. Ability to provide written informed consent. Mentally stable and able to comply with the procedures of the study protocol. Insulin-dependent diabetes mellitus Not otherwise eligible for an existing alloislet transplant protocol for type 1 diabetes mellitus Involvement in intensive diabetes management, defined by at least 3 injections daily or insulin pump therapy. Meets at least one of the following criteria despite intensive efforts made in close cooperation with their diabetic care team: Significant hypoglycemia unawareness or glycemic lability on conventional insulin therapy, as evidenced by at least one of the following at screening: Clarke score > 4 HYPO score >90th percentile (1047) Lability index (LI) >90th percentile (433 mM2/h/wk) A composite of a Clarke score of 4 or more and a HYPO score greater than or equal to the 75th percentile (423) and a LI greater than of equal to the 75th percentile (329) Progressive secondary complications as defined by end-stage renal disease necessitating dialysis or renal transplantation (eligible for islet after kidney or simultaneous islet kidney transplant) AND islet transplant appears to provide a more satisfactory benefit to risk ratio compared to pancreas transplantation (eg high surgical risk) Exclusion Criteria: HbA1c >10%. Untreated proliferative diabetic retinopathy. Uncontrolled Hypertension (SBP>160 or DBP>100) For female participants: Positive pregnancy test, presently breast-feeding, or unwillingness to use effective contraceptive measures for the duration of the study. Active infection including hepatitis B, hepatitis C, HIV, or TB as determined by a positive skin test or clinical presentation, or under treatment for suspected TB. Any history of malignancy except for completely resected squamous or basal cell carcinoma of the skin. Receiving treatment for a medical condition requiring chronic use of systemic steroids, except for use of prednisone <5 mg per day for kidney transplant recipients or physiologic hydrocortisone replacement. Persistent elevation of liver function tests at the time of study entry. Persistent SGOT (AST), SGPT (ALT), Alk Phos or total bilirubin, with values >1.5 times normal upper limits will exclude a patient. Severe co-existing cardiac disease, characterized by any one of these conditions: recent myocardial infarction (within past 6 months). evidence of ischemia on functional cardiac exam within the last year. left ventricular ejection fraction <30%. If diabetes is secondary to total pancreatectomy, participants will be considered only if >1 year out from surgery, medically stable, without severe issues with bowel function or pain management that may interfere with safe completion of the trial. History of alcoholism Any medical condition that, in the opinion of the investigator, will interfere with the safe completion of the trial.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Melena Bellin, MD
Phone
612-625-4686
Email
bell0130@umn.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bernhard J Hering, M.D.
Organizational Affiliation
University of Minnesota
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States
Individual Site Status
Available
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alisha Albrecht
Phone
612-624-8402
Email
albre441@umn.edu
First Name & Middle Initial & Last Name & Degree
Bernhard J Hering, M.D.
First Name & Middle Initial & Last Name & Degree
Melena Bellin, M.D.

12. IPD Sharing Statement

Learn more about this trial

Islet Transplant for Type 1 or Surgical Diabetes

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