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Islet Cell TransplantationPhase 1NCT00530686

Pancreatic Islet Cell Transplantation - A Novel Approach to Improve Islet Quality and Engraftment

A Phase 1 study testing Islet cell transplantation in people with Islet Cell Transplantation and 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
Islet Cell Transplantation, Type 1 Diabetes
What is being tested?
Islet cell transplantation
How many people
1 participants
Where
1 siteUnited States
Study dates
Jul 2008to Apr 2017
Phase
Phase 1
Are there results?
None posted in the registry

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 IRB approved informed consent form and is willing and able to follow study procedures for the full 24 months
  • Patient is expected to receive an islet cell transplant (up to 3 infusions) for type I diabetes mellitus
  • Type I diabetes mellitus 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 from a diabetology care team
  • Hypoglycemia unawareness, as defined by episodes of loss of cognitive function; or the inability to recognize glucose levels below 50 mg/dL; or frequent episodes of symptomatic hypoglycemia; or admission to the hospital for hypo/hyperglycemic
Show all 10Show fewer
  • Incapacitating signs and symptoms, as defined by the referring physician
  • HbA1c > 6.5
  • 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

  • Patient has previously received or is receiving an organ or bone marrow transplant
  • Patient has a known hypersensitivity to Tacrolimus, sirolimus, dacluzimab, 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
  • Glofil or Creatinine Clearance < 60 mL/min
Show all 35Show fewer
  • Serum Creatinine > 1.6 mg/dL consistently
  • Body mass index > 28
  • Malignancy other than basal cell carcinoma or squamous cell carcinoma
  • Radiographic evidence of pulmonary infection
  • Evidence of liver disease as evidenced by >2X ULN for AST, ALT, Alk Phos., or T bili.
  • Active infections
  • Hypercoagulable states (history of recurrent venous thrombosis, defined thrombophilia)
  • Bleeding / coagulation disorders
  • Basal C-Peptide > 0.3 ng/dL
  • HbA1c > 12%
  • Insulin requirement >0.7 IU/kg/day
  • Seropositivity for HIV, HBV, HCV, HTLV-1
  • Abnormal Pap smear, active gynecological infection
  • Positive exercise or chemical tolerance test
  • Patients currently under treatment for a medical condition requiring chronic use of steroids at a dose of prednisone >5mg/day will be excluded
  • Substance/alcohol abuse
  • Untreated proliferating diabetic retinopathy
  • PPD conversion or positive PPD without INH
  • No Primary care physician or primary care physician less than 6 months
  • Smoking in the last 6 months
  • Abnormal CBC / Hemoglobin < 12 g/dL
  • Macroalbuminuria > 300 mg/24 hours
  • Untreated hyperlipidemia - TC > 200 mg/dL, TGC > 200 mg/dL, LDL > 130 mg/dL
  • Untreated hyponatremia, hypokalemia, hypercalcemia, hypocalcemia
  • Iodine contrast allergy
  • PSA > 4
  • PRA > 20%
  • Active peptic ulcer disease/gallstones/hemangioma
  • Abnormal mammogram

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Annette C. & Harold C. Simmons Transplant Institute - Baylor University Medical Center, Dallas Texas, USA - Baylor All Saints Medical Center, Fort Worth Texas, USA

    Dallas, Texas, 75246

Other trials in United States

About this study

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

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.

Isolation of the islets from donor pancreata will occur in the Baylor University Medical Center Islet Cell Processing Laboratory (ICPL). The islet cell infusion is performed in the Interventional Radiology Suite at Baylor University Medical Center or Baylor All Saints Medical Center by an interventional radiologist. The procedure takes place in a suite designed for invasive procedures using sterile technique with access to general anesthesia if necessary. Following the procedure the patient is observed in the Interventional Radiology recovery area for as long as necessary as determined by a Physician and then transferred to the Transplant Service for an overnight stay. After recovery, the patient is admitted to the hospital on the Transplant Service for a 1-2 day observation.

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.

Being tested
Islet cell transplantation
Keywords
Diabetes Mellitus, Hypoglycemia, Hyperglycemia, Type 1 Diabetes, Islet cell transplantation
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 transplantationDrug

    The process is based on the enzymatic isolation of the pancreatic islets of Langerhans from an organ procured from a cadaveric donor; the islets obtained are injected into the liver of 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.

What is being measured

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

  1. 1)Presence or absence of hypoglycemic unawareness 2) To assess incidence of hypoglycemic episodes 3) To assess insulin requirements in patients who did not become insulin independent.

    Measured: 24 months

Secondary outcomes (1)
  1. To assess the achievement of insulin independence at 12 month and 24 month post transplant in patients who underwent allo islet cell transplantation.

    Measured: 12 months and 24 months

Timeline

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

  1. First posted17 Sep 2007 (estimated)
  2. Study startJul 2008
  3. Primary completionApr 2017
  4. Study completionApr 2017

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
Non-randomised
Intervention model
Single group
Masking
None (open label)
Enrolment
1 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00530686
Sponsor's protocol ID
008-095
Status last verified
Apr 2017
First submitted
13 Sep 2007
Last updated
24 Apr 2017
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Islet cell transplantation in people with Islet Cell Transplantation and 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 35 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 24 Apr 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

1)Presence or absence of hypoglycemic unawareness 2) To assess incidence of hypoglycemic episodes 3) To assess insulin requirements in patients who did not become insulin independent. (time frame: 24 months). 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 24 Apr 2017.

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