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Pancreatic Islet Transplantation Into the Gastric Submucosa

Primary Purpose

Type 1 Diabetes

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Isolated Human Pancreatic Islets
Sponsored by
Andrew Posselt
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes focused on measuring Insulin Dependent

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Key Inclusion Criteria:

  1. Primary islet allotransplant
  2. Type I diabetes mellitus for a minimum of 5 years
  3. One or more of the following signs or symptoms despite intensive efforts made in close cooperation with their diabetic care team:

    • Metabolic lability/instability characterized by hypoglycemia or ketoacidosis (>2 hospital admissions in the previous year), erratic glucose profiles (MAGE>120 mg/dL), or disruption in lifestyle of danger to life, self or others
    • Reduced awareness of hypoglycemia or >1 episode in the last 1.5 years of severe hypoglycemia
    • Persistently poor glucose control (as defined by HgbA1c>10% at the end of six months of Intensive management efforts with the diabetes care team)
    • Progressive secondary complications as defined by (i) a new proliferative retinopathy or clinically significant macular edema or therapy with photocoagulation during the last year; or (ii) symptomatic autonomic neuropathy (as defined by postural hypotension or neuropathic bladder)
  4. Age 18 and older
  5. Patients who have a renal transplant must have received their transplant at least 3 months previously and must have stable renal function (see exclusion criteria below)
  6. Must be able to give written informed consent

Exclusion Criteria:

Key Exclusion Criteria:

  1. Lymphopenia (<1000/µL) or leukopenia ( <3000 total leukocytes/µL)
  2. Presence of panel-reactive anti-HLA antibody >20%
  3. Positive lymphocytotoxic cross-match using donor lymphocytes and serum
  4. Evidence of acute EBV infection (IgM>IgG) OR no serologic evidence of previous exposure to EBV (IgG>IgM)
  5. Calculated or measured GFR < 50 ml/min/m2 in patients without a renal transplant.
  6. Calculated or measured GFR < 40 ml/min/m2 in patients with a renal transplant.
  7. Portal hypertension or history of significant liver disease
  8. History of malignancy within 10 years (except for treated basal or squamous cell CA of the skin)
  9. Active peptic ulcer disease or other gastric mucosal abnormalities as identified on screening endoscopy
  10. Severe unremitting diarrhea or other GI disorders potentially interfering with the ability to absorb oral medications
  11. Untreated proliferative retinopathy
  12. Pregnancy or breastfeeding
  13. Female subjects not post-menopausal or surgically sterile who are sexually active but not using an acceptable method of contraception
  14. Active infections
  15. Serologic evidence of infection with HIV, or HbsAg or HCV Ab positive
  16. Major ongoing psychiatric illness
  17. Ongoing substance abuse, drug or alcohol; or recent history of noncompliance
  18. Any condition that in the opinion of the Principal Investigator does not allow safe participation in the study

    -

Sites / Locations

  • University of California, San Francisco

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Study intervention

Arm Description

endoscopically-guided intestinal submucosal transplantation of Isolated Human Pancreatic Islets in a type 1 diabetic patient

Outcomes

Primary Outcome Measures

Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Hypo- and Hyper-glycemia limits for blood glucose related risks; during procedure, abdominal pain, duodenal hemorrhage, and duodenal perforation post-procedure, fever, cytokine release syndrome (to the thymoglobulin), immunosuppression related issues

Secondary Outcome Measures

Full Information

First Posted
April 3, 2012
Last Updated
October 2, 2020
Sponsor
Andrew Posselt
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1. Study Identification

Unique Protocol Identification Number
NCT01571817
Brief Title
Pancreatic Islet Transplantation Into the Gastric Submucosa
Official Title
Treatment of Type I Diabetes by Pancreatic Islet Transplantation Into The Gastric Submucosa
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
April 2012 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Andrew Posselt

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The overall objective of this pilot project is to evaluate the safety and efficacy of the gastric submucosal space as a novel site for clinical islet transplantation. The site has several physiologic attributes that may improve the outcomes of islet transplantation compared with the conventional intraportal transplant site.
Detailed Description
The overall objective of this pilot project is to evaluate the safety and efficacy of the gastric submucosal space as a novel site for clinical islet transplantation. Safety will be evaluated by the monitoring of side effects such as post procedural GI complications, frequency of hypo and hyperglycemic events, and immunosuppression side effects. Efficacy will be determined by accepted measures including insulin independence, long term glucose control, and reduction/elimination of hypoglycemic events. The site has several physiologic attributes that may improve the outcomes of islet transplantation compared with the conventional intraportal transplant site.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes
Keywords
Insulin Dependent

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study intervention
Arm Type
Experimental
Arm Description
endoscopically-guided intestinal submucosal transplantation of Isolated Human Pancreatic Islets in a type 1 diabetic patient
Intervention Type
Biological
Intervention Name(s)
Isolated Human Pancreatic Islets
Primary Outcome Measure Information:
Title
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Description
Hypo- and Hyper-glycemia limits for blood glucose related risks; during procedure, abdominal pain, duodenal hemorrhage, and duodenal perforation post-procedure, fever, cytokine release syndrome (to the thymoglobulin), immunosuppression related issues
Time Frame
Six months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Key Inclusion Criteria: Primary islet allotransplant Type I diabetes mellitus for a minimum of 5 years One or more of the following signs or symptoms despite intensive efforts made in close cooperation with their diabetic care team: Metabolic lability/instability characterized by hypoglycemia or ketoacidosis (>2 hospital admissions in the previous year), erratic glucose profiles (MAGE>120 mg/dL), or disruption in lifestyle of danger to life, self or others Reduced awareness of hypoglycemia or >1 episode in the last 1.5 years of severe hypoglycemia Persistently poor glucose control (as defined by HgbA1c>10% at the end of six months of Intensive management efforts with the diabetes care team) Progressive secondary complications as defined by (i) a new proliferative retinopathy or clinically significant macular edema or therapy with photocoagulation during the last year; or (ii) symptomatic autonomic neuropathy (as defined by postural hypotension or neuropathic bladder) Age 18 and older Patients who have a renal transplant must have received their transplant at least 3 months previously and must have stable renal function (see exclusion criteria below) Must be able to give written informed consent Exclusion Criteria: Key Exclusion Criteria: Lymphopenia (<1000/µL) or leukopenia ( <3000 total leukocytes/µL) Presence of panel-reactive anti-HLA antibody >20% Positive lymphocytotoxic cross-match using donor lymphocytes and serum Evidence of acute EBV infection (IgM>IgG) OR no serologic evidence of previous exposure to EBV (IgG>IgM) Calculated or measured GFR < 50 ml/min/m2 in patients without a renal transplant. Calculated or measured GFR < 40 ml/min/m2 in patients with a renal transplant. Portal hypertension or history of significant liver disease History of malignancy within 10 years (except for treated basal or squamous cell CA of the skin) Active peptic ulcer disease or other gastric mucosal abnormalities as identified on screening endoscopy Severe unremitting diarrhea or other GI disorders potentially interfering with the ability to absorb oral medications Untreated proliferative retinopathy Pregnancy or breastfeeding Female subjects not post-menopausal or surgically sterile who are sexually active but not using an acceptable method of contraception Active infections Serologic evidence of infection with HIV, or HbsAg or HCV Ab positive Major ongoing psychiatric illness Ongoing substance abuse, drug or alcohol; or recent history of noncompliance Any condition that in the opinion of the Principal Investigator does not allow safe participation in the study -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew M Posselt, M.D., Ph.D.
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States

12. IPD Sharing Statement

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Pancreatic Islet Transplantation Into the Gastric Submucosa

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