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Islet Transplantation in Type 1 Diabetes

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 determine the safety and effectiveness of islet transplantation, combined with immunosuppressive medications, for treating type 1 diabetes in individuals experiencing hypoglycemia unawareness and severe hypoglycemic episodes.

A tanulmány áttekintése

Részletes leírás

Type 1 diabetes is commonly treated with the administration of insulin, either by multiple insulin injections or by a continuous supply of insulin through a wearable pump. Insulin therapy allows long-term survival in individuals with type 1 diabetes; however, it does not guarantee constant normal blood sugar control. Because of this, long-term type 1 diabetic survivors often develop vascular complications, such as diabetic retinopathy, an eye disease that can cause poor vision and blindness, and diabetic nephropathy, a kidney disease that can lead to kidney failure. Some individuals with type 1 diabetes develop hypoglycemia unawareness, a life-threatening condition that is not easily treatable with medication and is characterized by reduced or absent warning signals for hypoglycemia. For such individuals, transplantation of pancreatic islets is a possible treatment option. Unfortunately, insulin independence among islet transplant recipients tends to decline over time. New strategies aimed at promoting engraftment of transplanted islets are needed to improve the clinical outcomes associated with this procedure. The purpose of this study is determine the safety and efficacy of islet transplantation, when combined with an immunosuppressive medication regimen, for treating type 1 diabetes in individuals experiencing hypoglycemia unawareness and severe hypoglycemic episodes. This study will also seek to improve the understanding of determinants of success and failure of islet transplants for type 1 diabetes.

Eligible participants will be randomly assigned to this study or a site-specific Phase 2 islet transplantation study. Participants in this study will receive up to three separate islet transplants and a regimen of immunosuppressive medications consisting of antithymocyte globulin (ATG), sirolimus, and low-dose tacrolimus.

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 islet transplant. 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 19 study visits following each transplant. A physical exam, review of adverse events, and blood collection will occur at most visits. A chest x-ray, abdominal ultrasound, electrocardiogram, quality of life questionnaires, urine collection, and glomerular filtrating rate (GFR) testing will occur at some visits. Participants will also test their own blood glucose levels at least five times per day throughout the study. A 24-month follow-up period will take place after the participant's last transplant.

Tanulmány típusa

Beavatkozó

Beiratkozás (Tényleges)

48

Fázis

  • 3. fázis

Kapcsolatok és helyek

Ez a rész a vizsgálatot végzők elérhetőségeit, valamint a vizsgálat lefolytatásának helyére vonatkozó információkat tartalmazza.

Tanulmányi helyek

    • California
      • San Francisco, California, Egyesült Államok, 94143
        • University of Callifornia, San Francisco
    • Florida
      • Miami, Florida, Egyesült Államok, 33136
        • University of Miami
    • Georgia
      • Atlanta, Georgia, Egyesült Államok, 30322
        • Emory University
    • Illinois
      • Chicago, Illinois, Egyesült Államok, 60611
        • Northwestern University
      • Chicago, Illinois, Egyesült Államok, 60612
        • University of Illinois, Chicago
    • Minnesota
      • Minneapolis, Minnesota, Egyesült Államok, 55455
        • University of Minnesota
    • Pennsylvania
      • Philadelphia, Pennsylvania, Egyesült Államok, 19104
        • University of Pennsylvania
    • Alberta
      • Edmonton, Alberta, Kanada, T6G028
        • University of Alberta

Részvételi kritériumok

A kutatók olyan embereket keresnek, akik megfelelnek egy bizonyos leírásnak, az úgynevezett jogosultsági kritériumoknak. Néhány példa ezekre a kritériumokra a személy általános egészségi állapota vagy a korábbi kezelések.

Jogosultsági kritériumok

Tanulmányozható életkorok

18 év (Felnőtt, Idősebb felnőtt)

Egészséges önkénteseket fogad

Nem

Tanulmányozható nemek

Összes

Leírás

Inclusion Criteria:

  • 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 a 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:

    1. Self-monitoring of glucose values no less than a mean of three times each day averaged over each week
    2. Administration of three or more insulin injections each day or insulin pump therapy
    3. 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 in the past 12 months, 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, compatible with hypoglycemia in which the individual required assistance of another subject was unable to treat him/herself person and which was associated with either a blood glucose level less than 54 mg/dl or prompt recovery after 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 specific definition of hypoglycemia unawareness, is in the protocol.

Exclusion Criteria:

  • 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/1.73mm2. More information about this criterion is in the protocol.
  • 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 4 months after study completion
  • Presence or history of active infection, including hepatitis B, hepatitis C, HIV, or tuberculosis.
  • 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:

    1. Heart attack within the last 6 months
    2. Evidence of ischemia on functional heart exam within the year prior to study entry
    3. 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 5 mg or less of prednisone daily, or an equivalent dose of hydrocortisone, for physiological replacement only
  • Treatment with any antidiabetic medication other than insulin within the past 4 weeks
  • Use of any study medications within the past 4 weeks
  • Received a live attenuated vaccine(s) 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.

Tanulási terv

Ez a rész a vizsgálati terv részleteit tartalmazza, beleértve a vizsgálat megtervezését és a vizsgálat mérését.

Hogyan készül a tanulmány?

Tervezési részletek

  • Elsődleges cél: Kezelés
  • Kiosztás: N/A
  • Beavatkozó modell: Egyetlen csoportos hozzárendelés
  • Maszkolás: Nincs (Open Label)

Fegyverek és beavatkozások

Résztvevő csoport / kar
Beavatkozás / kezelés
Kísérleti: Islet Transplantation
Participants will receive up to three separate islet transplants and a regimen of immunosuppressive medications consisting of antithymocyte globulin (ATG), sirolimus, and low-dose tacrolimus.
200 ml suspension of allogenic human purified islets
Participants will begin receiving ATG 2 days prior to the first islet transplant. ATG will continue to be given until Day 2 post-transplant.
Participants will begin receiving sirolimus 2 days prior to the first islet transplant and will be given for the duration of the study.
Más nevek:
  • Rapamycin
On Day 1 post-transplant, participants will receive tacrolimus, which will also be taken for the duration of the study.
Más nevek:
  • Fujimycin
  • FK-506
Etanercept will be taken on the day of transplant and Days 3, 7, and 10 post-transplant.
Transplantation of pancreatic islet cell
Basiliximab will be used in place of ATG for the second and third transplants, if they are necessary.
Más nevek:
  • kiméra egér-humán antiCD25
  • Ig gamma-1 chain C region

Mit mér a tanulmány?

Elsődleges eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Proportion of participants with a HbA1c less than 7.0% AND free of severe hypoglycemic events
Időkeret: From Day 28 to Day 365 (inclusive) following the first islet transplant, with the day of transplant designated Day 0
The proportion of participants with HbA1c ≤7.0% AND free of severe hypoglycemic events from Day 28 to Day 365 inclusive, following the first islet transplant, with the day of transplant designated Day 0.
From Day 28 to Day 365 (inclusive) following the first islet transplant, with the day of transplant designated Day 0

Másodlagos eredményintézkedések

Eredménymérő
Intézkedés leírása
Időkeret
Incidence and severity of adverse events related to the islet transplant procedure
Időkeret: 75 days following each transplant and 365 days following the first and final islet transplant
75 days following each transplant and 365 days following the first and final islet transplant
Incidence of worsening retinopathy
Időkeret: 365 days following the first islet transplant
365 days following the first islet transplant
Percent reduction in insulin requirements
Időkeret: 75 days following the first and subsequent islet transplant
75 days following the first and subsequent islet transplant
HbA1c on Day 75 Status Post the First and Subsequent Islet Transplant
Időkeret: 75 days following the first and subsequent islet transplant
The target level for HbA1c for this study is 7.0%. This value is the level recommended by the American Diabetes Association and is considered to be the clinically relevant goal for subjects with Type 1 diabetes (T1D). A HbA1c level of 6.5% is the goal recommended by the American College of Endocrinology.
75 days following the first and subsequent islet transplant
Mean amplitude of glycemic excursions (MAGE)
Időkeret: 75 days following the first and subsequent islet transplant
A MAGE >11.1 mmol/L (200 mg/dL) is indicative of marked glycemic lability.
75 days following the first and subsequent islet transplant
Glycemic liability index (LI)
Időkeret: 75 days following the first and subsequent islet transplant
75 days following the first and subsequent islet transplant
Ryan hypoglycemia severity score (HYPO)
Időkeret: 75 days following the first and subsequent islet transplant
75 days following the first and subsequent islet transplant
Basal (fasting) and 90-minute glucose and C-peptide derived from mixed meal tolerance test (MMTT)
Időkeret: 75 days following the first and subsequent islet transplant
75 days following the first and subsequent islet transplant
β-score on Day 75 Status Post the First and Subsequent Islet Transplant
Időkeret: 75 days following the first and subsequent islet transplant
Beta-score: an assessment of beta-cell function after islet transplantation.
75 days following the first and subsequent islet transplant
C-peptide:glucose creatinine ratio
Időkeret: 75 days following the first and subsequent islet transplant
75 days following the first and subsequent islet transplant
Acute insulin response to glucose, insulin sensitivity, and disposition index derived from the insulin-modified frequently sampled intravenous glucose tolerance (FSIGT) test
Időkeret: 75 days following the first and subsequent islet transplant
75 days following the first and subsequent islet transplant
Glucose variability and hypoglycemia duration derived from the continuous glucose monitoring system (CGMS)
Időkeret: 75 days following the first and subsequent islet transplant
75 days following the first and subsequent islet transplant
Assessment of Quality of Life Using the Short Form 36 Health Survey: Day 75 Status Post First and Final Islet Transplant
Időkeret: 75 days following the first and subsequent islet transplant
The Short-Form 36 Health Survey (SF-36®) is comprised of 36 items and 2 component scores, the Physical Component Score and the Mental Component Score. Each component is transformed into a 0-100 scale (higher numbers indicate greater quality of life) and normalized to have a mean of 50 and standard deviation of 10 for the 1998 general US population. SF-36 results unit of measure: Units on a Scale.
75 days following the first and subsequent islet transplant
Proportion of insulin-independent Participants on Day 365 Status Post the First and Final Islet Transplant
Időkeret: 365 days following the first and final islet transplant
365 days following the first and final islet transplant
Percent reduction in insulin requirements
Időkeret: 365 days following the first and final islet transplant
365 days following the first and final islet transplant
HbA1c on Day 365 Status Post the First and Final Islet Transplant
Időkeret: 365 days following the first and final islet transplant
The target level for HbA1c for this study is 7.0%. This value is the level recommended by the American Diabetes Association and is considered to be the clinically relevant goal for subjects with Type 1 diabetes (T1D). A HbA1c level of 6.5% is the goal recommended by the American College of Endocrinology.
365 days following the first and final islet transplant
MAGE
Időkeret: 365 days following the first and final islet transplant
A MAGE >11.1 mmol/L (200 mg/dL) is indicative of marked glycemic lability.
365 days following the first and final islet transplant
Glycemic liability index (LI): Day 365 Status Post First and Final Islet Transplant
Időkeret: 365 days following the first and final islet transplant
365 days following the first and final islet transplant
Clarke score
Időkeret: 365 days following the first and final islet transplant
The Clarke survey provides a composite indices of hypoglycemia frequency, severity, and symptom recognition.
365 days following the first and final islet transplant
HYPO score
Időkeret: 365 days following the first and final islet transplant
The HYPO(glycemia) score provides a composite indices of hypoglycemia frequency, severity, and symptom recognition.
365 days following the first and final islet transplant
Basal (fasting) and 90-minute glucose and C-peptide (MTT)
Időkeret: 365 days following the first and final islet transplant
365 days following the first and final islet transplant
β-score on Day 365 Status Post First and Final Islet Transplant
Időkeret: 365 days following the first and final islet transplant
Beta-score: an assessment of beta-cell function after islet transplantation.
365 days following the first and final islet transplant
C-peptide: glucose creatinine ratio
Időkeret: 365 days following the first and final islet transplant
365 days following the first and final islet transplant
Assessment of Quality of Life Using the Short Form 36 Health Survey: Day 365 Status Post First and Final Islet Transplant
Időkeret: 365 days following the first and final islet transplant
The Short-Form 36 Health Survey (SF-36®) is comprised of 36 items and 2 component scores, the Physical Component Score and the Mental Component Score. Each component is transformed into a 0-100 scale (higher numbers indicate greater quality of life) and normalized to have a mean of 50 and standard deviation of 10 for the 1998 general US population. SF-36 results unit of measure: Units on a Scale.
365 days following the first and final islet transplant
Proportion of participants receiving a second islet transplant
Időkeret: 365 days following the first and final islet transplant
365 days following the first and final islet transplant
Proportion of participants receiving a third islet transplant
Időkeret: 365 days following the first and final islet transplant
365 days following the first and final islet transplant
Incidence and severity of adverse events related to the immunosuppression therapy
Időkeret: 75 days following each transplant and 365 days following the first and final islet transplant
75 days following each transplant and 365 days following the first and final islet transplant
Incidence of a change in the immunosuppression drug regimen
Időkeret: 75 days following each transplant and 365 days following the first and final islet transplant
75 days following each transplant and 365 days following the first and final islet transplant
Incidence of immune sensitization defined by detecting anti-HLA antibodies not present prior to transplantation
Időkeret: 75 days following each transplant and 365 days following the first and final islet transplant
75 days following each transplant and 365 days following the first and final islet transplant
Proportion of insulin-independent participants on Day 75 Status Post First and Subsequent Islet Transplant
Időkeret: 75 days following first and subsequent islet transplant
75 days following first and subsequent islet transplant
Acute insulin response to glucose insulin sensitivity, and disposition index derived from the FSIGT test
Időkeret: 365 days following the first and final islet transplant
Frequently Sampled Intravenous Glucose Tolerance (FSIGT), a measure of insulin-independence, a clinically relevant measure of islet graft function.
365 days following the first and final islet transplant

Együttműködők és nyomozók

Itt találhatja meg a tanulmányban érintett személyeket és szervezeteket.

Nyomozók

  • Tanulmányi szék: Bernhard Hering, MD, University of Minnesota
  • Tanulmányi szék: Olle Korsgren, PhD, Uppsala University Hospital
  • Tanulmányi szék: Ali Naji, PhD, University of Pennsylvania
  • Tanulmányi szék: Camillo Ricordi, MD, University of Miami
  • Tanulmányi szék: James Shapiro, MD, PhD, University of Alberta
  • Tanulmányi szék: Andrew Posselt, MD, PhD, University of California, San Francisco
  • Tanulmányi szék: Nicole Turgeon, MD, Emory University
  • Tanulmányi szék: Xunrong Luo, MD, PhD, Northwestern Univerity

Publikációk és hasznos linkek

A vizsgálattal kapcsolatos információk beviteléért felelős személy önkéntesen bocsátja rendelkezésre ezeket a kiadványokat. Ezek bármiről szólhatnak, ami a tanulmányhoz kapcsolódik.

Általános kiadványok

Tanulmányi rekorddátumok

Ezek a dátumok nyomon követik a ClinicalTrials.gov webhelyre benyújtott vizsgálati rekordok és összefoglaló eredmények benyújtásának folyamatát. A vizsgálati feljegyzéseket és a jelentett eredményeket a Nemzeti Orvostudományi Könyvtár (NLM) felülvizsgálja, hogy megbizonyosodjon arról, hogy megfelelnek-e az adott minőség-ellenőrzési szabványoknak, mielőtt közzéteszik őket a nyilvános weboldalon.

Tanulmány főbb dátumok

Tanulmány kezdete

2006. október 1.

Elsődleges befejezés (Tényleges)

2012. szeptember 1.

A tanulmány befejezése (Tényleges)

2014. május 1.

Tanulmányi regisztráció dátumai

Először benyújtva

2007. február 9.

Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak

2007. február 9.

Első közzététel (Becslés)

2007. február 13.

Tanulmányi rekordok frissítései

Utolsó frissítés közzétéve (Tényleges)

2019. július 17.

Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak

2019. július 11.

Utolsó ellenőrzés

2019. július 1.

Több információ

A tanulmányhoz kapcsolódó kifejezések

Terv az egyéni résztvevői adatokhoz (IPD)

Tervezi megosztani az egyéni résztvevői adatokat (IPD)?

IGEN

IPD terv leírása

Participant level data access and additional relevant materials are available to researchers and the public at: https://www.immport.org/home.

The study Identifier in ImmPort is SDY1178.

IPD megosztási időkeret

The data is available. ImmPort is a long-term archive of clinical and mechanistic data.

IPD-megosztási hozzáférési feltételek

Register for ImmPort at: https://www.immport.org/registration and submit a rationale for the purpose of requesting study data access.

ImmPort is a long-term archive of clinical and mechanistic data, a National Institute of Allergy and Infectious Diseases Division of Allergy, Immunology and Transplantation (NIAID DAIT)-funded data repository. This archive is in support of the NIH mission to share data with the public. Data shared through ImmPort is provided by NIH-funded programs, other research organizations and individual scientists, ensuring these discoveries will be the foundation of future research.

Az IPD megosztását támogató információ típusa

  • STUDY_PROTOCOL
  • NEDV
  • ICF
  • ANALYTIC_CODE

Tanulmányi adatok/dokumentumok

  1. Tanulmányi Protokoll
    Információs azonosító: SDY1178
    Információs megjegyzések: ImmPort study ID is SDY1178.
  2. A leíró adatok és eredmények teljes készlete
    Információs azonosító: SDY1178
    Információs megjegyzések: ImmPort is a long-term archive of clinical and mechanistic data from DAIT-funded grants and contracts. This archive is in support of the NIH mission to share data with the public.

Gyógyszer- és eszközinformációk, tanulmányi dokumentumok

Egy amerikai FDA által szabályozott gyógyszerkészítményt tanulmányoz

Igen

Egy amerikai FDA által szabályozott eszközterméket tanulmányoz

Nem

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