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Type 1 DiabetesPhase 1NCT00214786

Pancreatic Islet Cell Transplantation

A Phase 1 study testing Islet cell transplantation in people with Type 1 Diabetes, run by Baylor Research Institute at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to assess a novel approach to immunosuppression in allogenic pancreatic islet cell transplant recipients. In addition, the study aims to assess remote site islet processing with culture for pancreatic islet cell transplantation in human subjects. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Type 1 Diabetes
What is being tested?
Islet cell transplantation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
4 participants
Where
1 siteUnited States
Study dates
Apr 2005to Jul 2007
Phase
Phase 1
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patient has been fully informed and has signed an Institutional Review Board (IRB) approved informed consent form and is willing and able to follow study procedures for the full 2 years
  • Patient is expected to receive an islet cell transplant (up to 3 infusions) for type I diabetes mellitus
  • Type I diabetes of more than 5 years duration
  • Age between 18 and 65
  • Unstable diabetes mellitus control, as defined by glucose measurements above 200 mg/dL and/or below 80 mg/dL despite adequate medical care
  • Hypoglycemia unawareness, as defined by episodes of loss of cognitive function
Show all 10Show fewer
  • Incapacitating signs and symptoms, as defined by the referring physician
  • Poor control of HbA1c > 8%
  • Psychogenically able to comply, in the opinion of the investigator
  • Female patients of childbearing potential must have a negative urine or serum pregnancy test upon hospitalization or within 7 days prior to enrollment and have agreed to utilize effective birth control throughout the study as well as for 6 weeks following study completion.

Who cannot join

  • Patients meeting any of the following criteria will be excluded from study participation.
  • Patient has previously received or is receiving an organ or bone marrow transplant
  • Patient has a known hypersensitivity to Tacrolimus, sirolimus, daclizumab, or CellCept
  • Patient is pregnant or lactating
  • Patient has participated in a blinded trial or participated in a trial involving a non-marketed (investigational) drug within 3 months of enrollment
  • Patient has participated in a trial involving a marketed drug or an infusion device within 30 days of the start of the trial
Show all 27Show fewer
  • Glomerular filtration rate (GLOFIL) < 60 mL/min
  • Serum Creatinine > 1.6 mg/dL consistently
  • Body mass index > 30
  • Autoimmune thyroiditis
  • Malignancy other than basal cell carcinoma or squamous cell carcinoma
  • Radiographic evidence of pulmonary infection
  • Evidence of liver disease
  • Portal hypertension
  • Active infections
  • Hypercoagulable states (history of recurrent venous thrombosis, defined thrombophilia)
  • Bleeding / coagulation disorders
  • Basal insulin C-Peptide > 0.3 ng/dL
  • Insulin C-peptide > 0.3 ng/dL during stimulation test
  • HbA1c > 12%
  • Insulin requirement > 1 IU/kg/day
  • Seropositivity for Human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), Human T-cell leukemia virus-1 (HTLV-1)
  • Abnormal Pap smear in the last two months, active gynecological infection
  • Positive exercise or chemical tolerance test
  • Steroid dependence
  • Substance/alcohol abuse
  • Untreated proliferating diabetic retinopathy aa) Purified protein derivative (PPD) conversion or positive PPD without isonicotinic acid hydrazide (INH) bb) No Primary care physician or primary care physician less than 6 months cc) Smoking in the last 6 months dd) Abnormal Complete Blood Count (CBC) / Hemoglobin < 12 g/dL ee) Macroalbuminuria > 300 mg/24 hours ff) History of thyroid disease other than autoimmune disease gg) Untreated hyperlipidemia - Total Cholesterol (TC) > 240 mg/dL, Triglycerides (TGC) > 200 mg/dL, Low Density Lipoprotein (LDL) > 140 mg/dL hh) Untreated hyponatremia, hypokalemia, hypercalcemia, hypocalcemia ii) Iodine contrast allergy jj) Prostate Specific Antigen (PSA) > 4 kk) Panel Reactive Antibody (PRA) > 20% ll) Active peptic ulcer disease/gallstones/hemangioma mm) Abnormal mammogram

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Baylor Regional Transplant Institute - Baylor University Medical Center

    Dallas, Texas, 75246

Other trials in United States

About this study

Official title: Pancreatic Islet Cell Transplantation - A Novel Approach to Immunosuppression and Validation of Remote Site Islet Cell Processing, Islet Cell Culture and Two-Layer Preservation

The purpose of this study is to assess a novel approach to immunosuppression in allogenic pancreatic islet cell transplant recipients. In addition, the study aims to assess remote site islet processing with culture for pancreatic islet cell transplantation in human subjects.

Read the detailed description

The purpose of this study is to assess a novel approach to immunosuppression in allogenic pancreatic islet cell transplant recipients. In addition, the study aims to assess remote site islet processing with culture for pancreatic islet cell transplantation in human subjects.

Detailed Description: Diabetes mellitus (DM) type I is a disease that has significant social and economical impact. The prevalence of the disease in the United States is about 120,000 in individuals aged 19 or less and 300,000 to 500,000 at all ages and 150 million worldwide.

So far there are no mechanical devices able to effectively adjust the dose of insulin injected according to the serum glucose in patients with DM. This leads to less than perfect sugar control, with episodes of hypoglycemia. Successful pancreas transplantation averts the need of insulin administration.

The emerging alternative to whole organ pancreas transplantation is pancreatic islet cell transplantation (ICT). The process is based on the enzymatic isolation of the pancreatic islets from an organ procured from a cadaver donor. The islets obtained are injected into the liver in the recipient via percutaneous catheterization of the portal venous system. This procedure allows the selective transplantation of the insulin-producing cell population avoiding open surgery as well as the transplantation of the duodenum and the exocrine pancreas and their related morbidity.

The initial efforts with ICT had only modest results. The immunosuppression regimen was similar to the one used in solid organ transplantation, based on high dose steroids and calcineurin inhibitors - both agents with diabetogenic effects. The results improved markedly with the changes in the manipulations of the islets, and the change in immunosuppression thus avoiding the higher doses of steroids and using sirolimus, tacrolimus and daclizumab initiated by the investigators group at the University of Alberta in Edmonton, Canada. Their protocol requires in general two islet cell infusions in order to attain the critical cell mass necessary to achieve insulin-independency. The changes in treatment were adopted as the Edmonton Protocol, which is used in several transplant centers, worldwide.

A novel approach to organ preservation uses the two-layer preservation technique. This allows for longer travel time for the eventual shipment of the pancreas to an islet cell processing facility remotely located from the donor procurement site.

The isolation of the islets from the donor pancreas will be performed at the Diabetes Research Institute in Miami, Florida, according to the standard currently used by that institution. The Diabetes Research Institute is a well-established center with a state-of-the-art islet cell isolation facility for the purpose of transplantation in humans, accredited and monitored by the FDA according to FDA standards.

The focus of the research in the ICT is centered on the development of a safe and effective procedure that will eventually replace surgical pancreas transplantation together with an ideal immunosuppressive regimen that provides safe and effective prevention against rejection, while minimizing the adverse events associated that negatively impact transplant recipient's quality of life.

This study is being conducted as a validation of the Edmonton protocol for ICT at our institution. Our aim is to test the efficacy of the use of the two-layer preservation technique for transport of the donor pancreas to the off-site processing facility and the use of islet cell culture in the off-site processing facility before the islet isolate is shipped to our center.

Conditions
Type 1 Diabetes
Being tested
Islet cell transplantation
Keywords
Diabetes Mellitus, Hypoglycemia, Hyperglycemia
Medical subject headings
Diabetes Mellitus, Type 1, Diabetes Mellitus, Hypoglycemia, Hyperglycemia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Islet cell transplantationBiological

    Allogenic islet transplantation

Study groups in NCT00214786
Study groupRoleWhat they receive
Islet Cell TransplantationExperimentalAllogenic islet cell transplantation
Receives: Biological: Islet cell transplantation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Achievement of Insulin Independence at 12-month Post Transplant

    To assess the number of patients who achieve insulin independence at 12-month after islet cell transplantation

    Measured: 12 months post transplant

Secondary outcomes (9)
  1. Presence or Absence of Hypoglycemic Unawareness

    Number of patients who achieved absence of hypoglycemic unawareness

    Measured: 12 months after transplantation

  2. Incidence of Hypoglycemic Episodes

    Blood glucose <70 mg/dl, number of times reported per month

    Measured: 12 months after transplantation

  3. Change of Insulin Requirements in Patients Who Did Not Become Insulin Independent

    Percentage of insulin requirement at month 12 against that at baseline in the patients who did not achieve insulin independence. The percentage less than 100% indicates that subjects reduced insulin requirements 12 months after islet transplantation when compared with those at pre-transplant, while the parentage more than 100% represents that patients needed higher amount of exogenous insulin 12 months after islet transplantation.

    Measured: 12 months after transplantation

  4. Islet Cell Mass Obtained After Remote Site Processing

    The sum of Islet mass obtained after transport using the two-layer preservation method, remote site processing and islet culture. Islet mass as defined by Islet Equivalent per kilogram recipient body weight.

    Measured: At transplantation

  5. The Number of Islet Cell Infusions Needed to Achieve Insulin Independence

    Measured: 12 months after transplantation

  6. Renal Function

    Glomerular filtration rate measured by sodium iothalamate I-125 injection (GLOFIL)

    Measured: 12 months after transplantation

  7. Morbidity Related to the Immunosuppression Regimen

    Number of participants who experienced serious adverse events related to immunosuppression regimen

    Measured: 12 months after transplantation

  8. Morbidity Related to the Islet Cell Infusion

    Number of participants who experienced serious adverse events related to islet cell infusion

    Measured: 12months after transplantation

  9. The Quality of Life of the Recipients Measured With the RAND 36-item Short Form Health Survey

    Averaged score in subscales of 'physical functioning', 'Role limitations due to emotional problems', 'energy/fatigue', 'emotional well-being', 'social functioning', 'pain' and 'general health' in the RAND 36-item short form health survey (SF-36). Full scale range is 0-100 for all subscales with 100 as the best outcome and 0 as the worst outcome.

    Measured: 12 months after transplantation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Sep 2005 (estimated)
  2. Study startApr 2005
  3. Primary completionJul 2007
  4. Study completionJul 2007

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
4 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00214786
Sponsor's protocol ID
003-040
Status last verified
Jun 2017
First submitted
14 Sep 2005
Last updated
14 Jun 2017
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Islet cell transplantation in people with Type 1 Diabetes, run by Baylor Research Institute at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 10 inclusion and 27 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 14 Jun 2017. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 6 Jun 2014). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Achievement of Insulin Independence at 12-month Post Transplant (time frame: 12 months post transplant). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jun 2017.

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