Pancreatic Islet Transplantation Into the Gastric Submucosa

NCT ID: NCT01571817

Last Updated: 2020-10-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 1 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-04-30
• Study Completion Date: 2014-12-31

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.

Conditions

Type 1 Diabetes

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Study intervention

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

Group Type: EXPERIMENTAL

Isolated Human Pancreatic Islets

Intervention Type: BIOLOGICAL

Interventions

Isolated Human Pancreatic Islets

Intervention Type: BIOLOGICAL

Eligibility Criteria

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

Exclusion Criteria

6. Must be able to give written informed consent

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

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• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 90 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Andrew Posselt

OTHER

Sponsor Role: lead

Responsible Party

Andrew Posselt

Principal Investigator

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Andrew M Posselt, M.D., Ph.D.

Role: PRINCIPAL_INVESTIGATOR

University of California, San Francisco

Locations

University of California, San Francisco

San Francisco, California, United States

Countries

United States

Other Identifiers

Islet-Tx-Sub-DERC

Identifier Type: -

Identifier Source: org_study_id