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Diabetes Mellitus, Type 1Phase 2NCT00434850

Peritransplant Deoxyspergualin in Islet Transplantation in Type 1 Diabetes

A Phase 2 study testing Allogeneic Pancreatic Islet Cells, Deoxyspergualin and Antithymocyte globulin in people with Diabetes Mellitus, Type 1, run by National Institute of Allergy and Infectious Diseases (NIAID) at 3 sites 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

Type 1 diabetes is an autoimmune disease in which the insulin-producing pancreatic beta cells are destroyed, resulting in poor blood sugar control. The purpose of this study is to assess the safety and efficacy of deoxyspergualin (DSG), an immunosuppressant drug, on post-transplant islet function in people with type 1… Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Diabetes Mellitus, Type 1
What is being tested?
Allogeneic Pancreatic Islet Cells, Deoxyspergualin and Antithymocyte globulin
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
14 participants
Where
3 sitesUnited States
Study dates
Oct 2006to Nov 2013
Phase
Phase 2
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

  • Mentally stable and able to comply with study procedures
  • Clinical history compatible with type 1 diabetes, with onset of disease at less than 40 years of age; insulin dependence for at least 5 years at study entry; AND sum of age and insulin-dependent diabetes duration of at least 28
  • Absent stimulated C-peptide (less than 0.3 ng/ml) 60 and 90 minutes post mixed-meal tolerance test
  • Involvement of intensive diabetes management, defined as:
  • Self monitoring of glucose values no less than a mean of three times each day, averaged over each week
  • Administration of three or more insulin injections each day or insulin pump therapy
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  • Under the direction of an endocrinologist, diabetologist, or diabetes specialist, with at least three clinical evaluations during the past 12 months prior to study enrollment
  • At least one episode of severe hypoglycemia, defined as an event with one of the following symptoms: memory loss; confusion; uncontrollable behavior; irrational behavior; unusual difficulty in awakening; suspected seizure; seizure; loss of consciousness; or visual symptoms, in which the participant was unable to treat him/herself and which was associated with either a blood glucose level less than 54 mg/dl or prompt recovery after an oral carbohydrate, intravenous glucose, or glucagon administration in the 12 months prior to study enrollment.
  • Reduced awareness of hypoglycemia. More information about this criterion, including the specific definition of hypoglycemia unawareness, is in the protocol.

Who cannot join

  • Body mass index (BMI) greater than 30 kg/m2 or weight less than or equal to 50 kg
  • Insulin requirement of more than 1.0 IU/kg/day or less than 15 U/day
  • HbA1c greater than 10%
  • Untreated proliferative diabetic retinopathy
  • Systolic blood pressure higher than 160 mmHg or diastolic blood pressure higher than 100 mmHg
  • Measured glomerular filtration rate using iohexol of less than 80 ml/min/1.73m2. More information about this criterion is in the protocol.
Show all 35Show fewer
  • Presence or history of macroalbuminuria (greater than 300 mg/g creatinine)
  • Presence or history of panel-reactive anti-HLA antibody levels greater than background by flow cytometry. More information about this criterion is in the protocol.
  • Pregnant, breastfeeding, or unwilling to use effective contraception throughout the study and for 4 months after study completion
  • Active infection, including hepatitis B virus, hepatitis C virus, HIV, or tuberculosis. More information about this criterion is in the protocol.
  • Negative for Epstein-Barr virus by IgG determination
  • Invasive aspergillus, histoplasmosis, or coccidioidomycosis infection in the past year
  • History of malignancy except for completely resected squamous or basal cell carcinoma of the skin
  • Known active alcohol or substance abuse
  • Baseline Hgb below the lower limits of normal, lymphopenia, neutropenia, or thrombocytopenia
  • History of Factor V deficiency
  • Any coagulopathy or medical condition requiring long-term anticoagulant therapy after transplantation or individuals with an INR greater than 1.5
  • Severe coexisting cardiac disease, characterized by any one of the following conditions:
  • Heart attack within the last 6 months
  • Evidence of ischemia on functional heart exam within the year prior to study entry
  • Left ventricular ejection fraction less than 30%
  • Persistent elevation of liver function tests at the time of study entry
  • Symptomatic cholecystolithiasis
  • Acute or chronic pancreatitis
  • Symptomatic peptic ulcer disease
  • Severe unremitting diarrhea, vomiting, or other gastrointestinal disorders that could interfere with the ability to absorb oral medications
  • Hyperlipidemia despite medical therapy, defined as fasting LDL cholesterol greater than 130 mg/dl (treated or untreated) and/or fasting triglycerides greater than 200 mg/dl
  • Currently receiving treatment for a medical condition that requires chronic use of systemic steroids except for the use of less than or equal to 5 mg prednisone daily, or an equivalent dose of hydrocortisone, for physiological replacement only
  • Treatment with any anti-diabetic medication other than insulin within 4 weeks prior to study entry
  • Use of any study medications within the past 4 weeks
  • Received a live attenuated vaccine within the past 2 months
  • Any medical condition that, in the opinion of the investigator, might interfere with safe participation in the trial
  • Treatment with any immunosuppressive regimen at the time of enrollment.
  • A previous islet transplant.
  • A previous pancreas transplant, unless the graft failed within the first week due to thrombosis, followed by pancreatectomy and the transplant occurred more than 6 months prior to enrollment

Trial locations and contacts

3 sites in 1 country.

United States3 sites
  • Northwestern University

    Chicago, Illinois, 60611

  • University of Minnesota

    Minneapolis, Minnesota, 55455

  • University of Californinia, San Francisco

    San Francisco, California, 94143

Other trials in United States

About this study

Official title: Peritransplant Deoxyspergualin in Islet Transplantation in Type 1 Diabetes (CIT-03)

Type 1 diabetes is an autoimmune disease in which the insulin-producing pancreatic beta cells are destroyed, resulting in poor blood sugar control. The purpose of this study is to assess the safety and efficacy of deoxyspergualin (DSG), an immunosuppressant drug, on post-transplant islet function in people with type 1 diabetes who have not responded to intensive insulin therapy.

Read the detailed description

Type 1 diabetes, also known as insulin-dependent diabetes, is a chronic disease in which the pancreas produces insufficient insulin to properly regulate blood sugar levels. Hypoglycemia, low blood sugar, and hyperglycemia, high blood sugar, can lead to significant complications in people with type 1 diabetes. Intensive insulin therapy has been shown to reduce the risk of chronic complications in people who achieve near normalization of glycemia. However, this therapy is labor intensive, difficult to implement, and associated with an increased frequency of severe hypoglycemia. Transplantation of islets from a healthy pancreas has been successful in restoring normal blood sugar levels and has led to initial insulin independence in people with type 1 diabetes. Rejection of these islets by the recipient's immune system, however, makes the treatment ineffective within a couple of years. Immunosuppressant drugs may be an effective way to maintain islet function post-transplant. The purpose of this study is to assess the safety and efficacy of an immunosuppressive regimen that includes DSG on post-transplant islet function in people with type 1 diabetes who have not responded to intensive insulin therapy. The study will also seek to improve the understanding of determinants of success and failure of islet transplants for type 1 diabetes.

Following screening procedures and 2 days prior to islet transplant, participants will be randomly assigned to either this Phase 2 trial or a multicenter Phase 3 trial. Participants in this study will receive up to three separate islet transplants. They will begin receiving antithymocyte globulin (ATG) and sirolimus 2 days prior to the first islet transplant. ATG will continue to be given until Day 2 post-transplant. Participants will continue taking sirolimus for the duration of the study. On the day of transplant, participants will receive DSG and etanercept, in addition to ATG and sirolimus. The DSG infusion will be administered over 3 hours and will immediately precede the islet transplant. Participants will continue receiving daily 3-hour infusions of DSG through Day 6 post-transplant. Etanercept will also be administered on Days 3, 7, and 10 post-transplant. Tacrolimus will be administered on Day 1 post-transplant and continued throughout the study.

Transplantations will involve an inpatient hospital stay and infusion of islets into a branch of the portal vein. Participants who do not achieve or maintain insulin independence by Day 75 post-transplant will be considered for a second islet transplant. Participants who remain dependent on insulin for longer than 1 month after the second transplant and who show partial graft function will be considered for a third transplant. Daclizumab or basiliximab will be used in place of ATG for the second and third transplants, if they are necessary. Participants who do not meet the criteria for a subsequent transplant and do not have a functioning graft will enter a reduced follow-up period.

There will be up to 21 study visits following each transplant. A physical exam, review of adverse events, blood collection, urine tests, and measures of immunosuppression levels will occur at most visits. An abdominal ultrasound and glomerular filtration rate testing will occur at some study visits. Participants will also self-test their glucose levels at least five times per day throughout the study. A 12-month follow-up period will take place after the participant's last transplant.

Being tested
Allogeneic Pancreatic Islet Cells, Deoxyspergualin, Antithymocyte globulin, Daclizumab or basiliximab, Sirolimus
Keywords
Insulin dependence, Hypoglycemia, Hyperglycemia unawareness
Medical subject headings
Diabetes Mellitus, Type 1, Hypoglycemia

What participants receive

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

  • Allogeneic Pancreatic Islet CellsBiological

    Preparation of allogeneic pancreatic islet cells injected into the portal vein of the liver

  • DeoxyspergualinDrug

    An anti-inflammatory agent that blocks proinflammatory cytokine production and inhibits T-cells and B-cells and affects antigen presenting cells.

  • Antithymocyte globulinBiological

    Immunosuppressive that selectively depletes activated T-cells and depletes resting T-cells in a dose-dependent manner.

  • Daclizumab or basiliximabBiological

    Will replace antithymocyte globulin in all islet transplantations after the first one

  • SirolimusDrug

    Maintenance immunosuppressive therapy

  • TacrolimusDrug

    Maintenance immunosuppressive therapy

  • EtanerceptBiological

    Blocks TNF-alpha which is toxic to islet cells

Study groups in NCT00434850
Study groupRoleWhat they receive
Allogeneic Pancreatic Islet CellsExperimentalParticipants in this study can receive up to three separate islet transplants. They will begin receiving antithymocyte globulin (ATG) and sirolimus 2 days prior to the first islet transplant. ATG will continue to be given until Day 2 post-transplant. Participants will continue taking sirolimus for the duration of the study. On the day of transplant, participants will receive DSG and etanercept, in addition to ATG and sirolimus. The DSG infusion will be administered over 3 hours and will immediately precede the islet transplant. Participants will continue receiving daily 3-hour infusions of DSG through Day 6 post-transplant. Etanercept will also be administered on Days 3, 7, and 10 post-transplant. Tacrolimus will be administered on Day 1 post-transplant and continued throughout the study.
Receives: Biological: Allogeneic Pancreatic Islet Cells; Drug: Deoxyspergualin; Biological: Antithymocyte globulin; Biological: Daclizumab or basiliximab; Drug: Sirolimus; Drug: Tacrolimus; Biological: Etanercept

What is being measured

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

  1. Proportion of Insulin-independent Subjects

    Measured: 75 days following the first islet transplant

Secondary outcomes (30)
  1. Percent Reduction in Insulin Requirements

    Measured: 75 days following the first and subsequent islet transplant

  2. Hemoglobin A1c (HbA1c)

    Measured: 75 days following the first and subsequent islet transplant

  3. Mean Amplitude of Glycemic Excursions (MAGE)

    Measured: 75 days following the first and subsequent islet transplant

  4. Glycemic Lability Index (LI)

    Measured: 75 days following the first and subsequent islet transplant

  5. Ryan Hypoglycemia Severity Score (HYPO)

    Measured: 75 days following the first and subsequent islet transplant

  6. Basal (fasting) and 90-minute Glucose and C-peptide Results

    Derived from Mixed Meal Tolerance Test (MMTT)

    Measured: 75 days following the first and subsequent islet transplant

  7. Beta-score

    Assesses beta-cell function after islet transplantation

    Measured: 75 days following the first and subsequent islet transplant

  8. C-peptide: Glucose Creatinine Ratio

    Measured: 75 days following the first and subsequent islet transplant

  9. Acute Insulin Response to Glucose, Insulin Sensitivity, and Disposition Index

    Derived from the insulin-modified frequently sampled intravenous glucose tolerance (FSIGT) test

    Measured: 75 days following the first and subsequent islet transplant

  10. Glucose Variability and Hypoglycemia Duration

    Derived from the continuous glucose monitoring system (CGMS)

    Measured: 75 days following the first and subsequent islet transplant

  11. Quality of Life (QOL) Measure

    Measured: 75 days following the first and subsequent islet transplant

  12. Incidence of Worsening Retinopathy

    Measured: 365 days following the first islet transplant

  13. Proportion of Insulin-independent Subjects

    Measured: 365 days following the first and final islet transplant

  14. Percent Reduction in Insulin Requirements

    Measured: 365 days following the first and final islet transplant

  15. Hemoglobin A1c (HbA1c)

    Measured: 365 days following the first and final islet transplant

  16. Mean Amplitude of Glycemic Excursions (MAGE)

    Measured: 365 days following the first and final islet transplant

  17. Glycemic Lability Index (LI)

    Measured: 365 days following the first and final islet transplant

  18. Clarke Score

    A hypoglycemia score

    Measured: 365 days following the first and final islet transplant

  19. HYPO Score

    A hypoglycemia score

    Measured: 365 days following the first and final islet transplant

  20. Basal (fasting) and 90-minute Glucose and C-peptide

    Derived from Mixed Meal Tolerance Test (MMTT)

    Measured: 365 days following the first and final islet transplant

  21. Beta-score

    Assesses beta-cell function after islet transplantation

    Measured: 365 days following the first and final islet transplant

  22. C-peptide: Glucose Creatinine Ratio

    Measured: 365 days following the first and final islet transplant

  23. Quality of life (QOL) Measure

    Measured: 365 days following the first and final islet transplant

  24. Proportion of Subjects Receiving a Second Islet Cell Transplant

    Measured: 365 days following the first islet transplant

  25. Proportion of Subjects Receiving a Third Islet Cell Transplant

    Measured: 365 days following the first and final islet transplant

  26. Incidence and Severity of Adverse Events Related to the Islet Cell Transplant Procedure

    Measured: 75 days and 365 days following the first and final islet cell infusion

  27. Incidence and Severity of Adverse Events Related to the Immunosuppression Therapy

    Measured: 75 days and 365 days following the first and final islet transplant

  28. Incidence of a Change in the Immunosuppression Drug Regimen

    Measured: 75 days and 365 days following the first and final islet cell transplant

  29. Incidence of Immune Sensitization

    Defined by detecting anti-HLA antibodies not present prior to transplantation

    Measured: 75 days and 365 days following the first and final islet transplant

  30. Acute Insulin Response to Glucose, Insulin Sensitivity, and Disposition Index (DI)

    Derived from the insulin-modified frequently sampled intravenous glucose tolerance (FSIGT) test

    Measured: 365 day following the first and final islet transplant

Timeline

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

  1. First posted13 Feb 2007 (estimated)
  2. Study startOct 2006
  3. Primary completionSep 2011
  4. Study completionNov 2013

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 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
14 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00434850
Sponsor's protocol ID
DAIT CIT-03
Status last verified
Feb 2016
First submitted
9 Feb 2007
Last updated
16 Mar 2016
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Allogeneic Pancreatic Islet Cells, Deoxyspergualin and Antithymocyte globulin in people with Diabetes Mellitus, Type 1, run by National Institute of Allergy and Infectious Diseases (NIAID) at 3 sites 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 9 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 16 Mar 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites 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 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

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?

Proportion of Insulin-independent Subjects (time frame: 75 days following the first islet 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 16 Mar 2016.

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