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Pancreas bionico nella CFRD

6 novembre 2026 aggiornato da: Jaeb Center for Health Research

Uno studio randomizzato sul pancreas bionico a base di sola insulina nel diabete correlato alla fibrosi cistica

This multi-center randomized controlled trial (RCT) will compare efficacy and safety endpoints using the insulin-only configuration of the iLet Bionic Pancreas System (BP) versus a control group using their usual care insulin delivery method and continuous glucose monitoring (CGM) during a 13-week study period in individuals ≥14 years old with cystic fibrosis-related diabetes (CFRD). After 13 weeks, participants will continue in a 13-week Extension Phase in which the BP group will continue to use the BP system and the Usual Care group will initiate use of the BP system.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

150

Fase

  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Colorado
      • Aurora, Colorado, Stati Uniti, 80045
        • University of Colorado-Barbara Davis Center for Diabetes
    • Connecticut
      • New Haven, Connecticut, Stati Uniti, 06511
        • Yale University School of Medicine
    • Georgia
      • Atlanta, Georgia, Stati Uniti, 30329
        • Emory University
    • Indiana
      • Indianapolis, Indiana, Stati Uniti, 46202
        • Indiana University School of Medicine
    • Maryland
      • Baltimore, Maryland, Stati Uniti, 21287
        • Johns Hopkins University School of Medicine
    • Massachusetts
      • Boston, Massachusetts, Stati Uniti, 02114
        • Massachusetts General Hospital
    • Minnesota
      • Minneapolis, Minnesota, Stati Uniti, 55455
        • University of Minnesota
    • Missouri
      • Kansas City, Missouri, Stati Uniti, 64108
        • Children's Mercy Hospital
    • New York
      • New York, New York, Stati Uniti, 10032
        • Columbia University Medical Center
    • Ohio
      • Cleveland, Ohio, Stati Uniti, 44106
        • University Hospitals of Cleveland
    • Pennsylvania
      • Philadelphia, Pennsylvania, Stati Uniti, 19104
        • Children's Hospital of Philadelphia
    • Texas
      • Dallas, Texas, Stati Uniti, 75235
        • UT Southwestern Medical Center
      • Houston, Texas, Stati Uniti, 77030
        • Baylor College of Medicine
      • San Antonio, Texas, Stati Uniti, 78207
        • University of Texas Health San Antonio
    • Utah
      • Salt Lake City, Utah, Stati Uniti, 84132
        • University of Utah
    • Virginia
      • Charlottesville, Virginia, Stati Uniti, 22903
        • University of Virginia-Center for Diabetes Technology

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

14 anni e precedenti (Bambino, Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion

  1. Age ≥ 14 years old at time of signing informed consent

  2. Able to provide informed consent (and assent for participants <18 years old)

  3. Documentation of a CF diagnosis as evidenced by one or more clinical features consistent with the CF phenotype and one or more of the following criteria:

    • Sweat chloride equal to or greater than 60 mmol/liter by quantitative pilocarpine iontophoresis test (QPIT) (when not taking a cystic fibrosis transmembrane conductance regulator (CFTR) modulator)
    • Two well-characterized mutations in the CFTR gene
  4. Clinical diagnosis of CFRD, defined as a person with CF and diabetes mellitus, treated with insulin for ≥3 months prior to screening

  5. Using the same insulin regimen for ≥1 month prior to screening and collection of baseline CGM data, with no plans to change regimen during the study: either multiple daily injections of insulin (MDI), basal-only without bolus insulin, an insulin pump without automation, or an automated insulin delivery (AID) system other than the BP (which is an exclusion)

  6. Total daily insulin dose must be ≥0.1 units/kg

  7. Able to speak and read English sufficient to understand the pump user interface and provide written materials for safe operation of the BP

    • For pediatric participants, this applies to both the participant and caregiver

  8. For participants <18 years old, living with one or more parent/legal guardian knowledgeable about emergency procedures for severe hypoglycemia. A designated care partner must be willing to be linked to the participant's Dexcom Follow application with location sharing on.

  9. For participants >18 years old who live alone, participant has a relative or acquaintance who lives within 30 minutes of participant and is willing to be contacted to check on participant if study staff feel that participant may be experiencing a medical emergency and cannot be reached. A designated care partner must be willing to be linked to the participant's Dexcom Follow application with location sharing on.

  10. No use of a non-insulin glucose-lowering medication, except metformin, that is not approved for use in T1D within 3 months prior to signing informed consent and willing to not use any such medications during the course of the trial. Note: such drugs cannot be used even if prescribed for weight loss rather than glucose-lowering.

  11. If not currently using a rapid-acting insulin that is approved for use in the iLet pump, willing and able to switch to an approved insulin when using the BP.

  12. Participant has commercial glucagon available for treatment of severe hypoglycemia or will obtain it prior to randomization

  13. Willing to authorize the study team to contact the participant's primary physician to inform them about their participation in this study.

  14. Enrolled in the Cystic Fibrosis Foundation Patient Registry (participants may enroll in the Registry at the time of enrollment if not already enrolled).

  15. No plans for trips of more than 14 consecutive days outside the United States during the period of study participation

  16. Investigator believes that the participant can safely use the iLet and will follow the protocol • The investigator will take into account the participant's HbA1c level (there is no upper limit for eligibility), compliance with current diabetes management, prior acute diabetic complications, cognitive ability, and general medical condition. For this reason, there is no upper limit on HbA1c specified for eligibility.

Exclusion

  1. Current use of the BP or an AID system not FDA approved for T1D

  2. Known hemoglobinopathy (sickle cell trait is not an exclusion)

  3. Current participation in another diabetes-related interventional trial

  4. Established history of allergy or severe reaction to adhesive or tape that must be used in the study

  5. Pregnant (positive urine hCG), breast feeding, plan to become pregnant in the next 7 months, or sexually active and can become pregnant but not using contraception

  6. Current use of hydroxyurea or unable to avoid hydroxyurea use during the study (interferes with accuracy of Dexcom sensor)

  7. Have started or stopped a CFTR modulator in the 4 weeks prior to screening.

    • Modifications of the dosing of a CFTR modulator is acceptable

  8. Anticipated lung or liver transplant (on transplant list)

  9. Lung or liver transplant within one year prior to screening. If they have had a transplant more than a year ago, but they:

    • Have had a rejection episode occur in prior 8 weeks, individual is excluded.
    • Their doses of corticosteroids and/or calcineurin inhibitors have not been stable for one month prior to enrollment and/or is expected to change significantly over the course of the study, individual is excluded.
  10. Acute pulmonary exacerbation or hospitalization within the 4 weeks prior to screening or treatment with IV antibiotics in the 4 weeks prior to screening

  11. History of a complete pancreatectomy

  12. Currently using enteral tube feedings for nutritional support

  13. Presence of a medical condition or use of a medication that, in the judgment of the investigator, clinical protocol chair, or medical monitor, could compromise the results of the study or the safety of the participant. Conditions to be considered by the investigator may include the following:

    • Alcohol or drug abuse
    • Use of prescription drugs that may dull the sensorium, or hinder decision-making during the period of participation in the study such has opioids or short-acting benzodiazepines
    • Coronary artery disease that is not stable with medical management, including unstable angina, angina that prevents moderate exercise (e.g., climbing a flight of stairs) despite medical management; or within the last 12 months before screening: a history of myocardial infarction, percutaneous coronary intervention, enzymatic lysis of a presumed coronary occlusion, or coronary artery bypass grafting
    • Congestive heart failure with New York Heart Association (NYHA) Functional Classification III or IV
    • History of TIA or stroke in the last 12 months
    • Severe liver disease such as end-stage cirrhosis
    • Renal failure requiring dialysis or known eGFR <30
    • Untreated or inadequately treated mental illness
    • History of untreated or inadequately treated eating disorder within the last 2 years, such as anorexia, bulimia, or diabulimia or omission of insulin to manipulate weight
    • History of intentional, inappropriate administration of insulin leading to severe hypoglycemia requiring treatment
  14. Employed by, or having immediate family members employed by Beta Bionics, or being directly involved in conducting the clinical trial, or having a direct supervisor at place of employment who is also directly involved in conducting the clinical trial (as a study investigator, coordinator, etc.); or having a first-degree relative who is directly involved in conducting the clinical trial.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: UC Group

Participants randomized to the Usual Care (UC) group will use their existing insulin delivery method in conjunction with a study CGM during the first 13-week of the study (RCT phase). The UC group will then initiate use of the BP System for the remaining 13 weeks of the study (Extension Phase).

The iLet Bionic Pancreas System (BP) consists of an integrated infusion pump, touchscreen display, Bluetooth radio, and insulin dosing algorithms, that automatically controls insulin delivery based on glucose values obtained by communicating with a CGM sensor.

Usual Care consists in the participant existing insulin therapy (prior to enrollment) in conjunction with a study CGM. Existing insulin therapies are defined as multiple daily injections of insulin (MDI) or use of an insulin pump.

Sperimentale: BP Group

Participants randomized to the intervention group will use the BP group using the iLet Bionic Pancreas System (BP) and continuous glucose monitoring (CGM) during the first 13-week of the study (RCT phase). After the RCT phase, participants will continue in a 13-week Extension Phase in which the BP group will continue to use the BP system.

The iLet Bionic Pancreas System (BP) consists of an integrated infusion pump, touchscreen display, Bluetooth radio, and insulin dosing algorithms, that automatically controls insulin delivery based on glucose values obtained by communicating with a CGM sensor.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
CGM-measured Time In Target Range of 70-180 mg/dL (TIR)
Lasso di tempo: 13 weeks

CGM-measured time in target range of 70-180 mg/dL (TIR)

13 weeks

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
CGM-measured Time In Range <54 mg/dL
Lasso di tempo: 13 weeks

CGM-measured time in range <54 mg/dL

13 weeks

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
CGM-measured Mean Glucose
Lasso di tempo: 13 weeks

Average glucose value measured by CGM

13 weeks
CGM-measured Time In Range >180 mg/dL
Lasso di tempo: 13 weeks

CGM-measured time in range >180 mg/dL

13 weeks
CGM-measured Time In Range >250 mg/dL
Lasso di tempo: 13 weeks

CGM-measured time in range >250 mg/dL

13 weeks
HbA1c At 13 Weeks
Lasso di tempo: 13 weeks

HbA1c at 13 weeks

13 weeks
Glucose Variability Measured With the Standard Deviation (SD)
Lasso di tempo: 13 weeks

Glucose variability measured with the standard deviation (SD)

13 weeks
CGM-measured Time In Range <70 mg/dL
Lasso di tempo: 13 weeks

CGM-measured time in range <70 mg/dL

13 weeks
Glucose Variability With the Coefficient of Variation (CV)
Lasso di tempo: 13 weeks

Glucose variability with the coefficient of variation (CV)

13 weeks
HbA1c <7.0% At 13 Weeks
Lasso di tempo: 13 weeks

HbA1c <7.0% at 13 weeks

13 weeks
HbA1c <7.0% At 13 Weeks In Participants With Baseline HbA1c >7.5%
Lasso di tempo: 13 weeks

HbA1c <7.0% at 13 weeks in participants with baseline HbA1c >7.5%

13 weeks
HbA1c <8.0% At 13 Weeks
Lasso di tempo: 13 weeks

HbA1c <8.0% at 13 weeks

13 weeks
HbA1c Improvement From Baseline To 13 Weeks >0.5%
Lasso di tempo: 13 weeks

HbA1c improvement from baseline to 13 weeks >0.5%

13 weeks
HbA1c Improvement From Baseline To 13 Weeks >1.0%
Lasso di tempo: 13 weeks

HbA1c improvement from baseline to 13 weeks >1.0%

13 weeks
HbA1c Improvement From Baseline To 13 Weeks >1.0% Or HbA1c <7.0% At 13 Weeks
Lasso di tempo: 13 weeks

HbA1c improvement from baseline to 13 weeks >1.0% or HbA1c <7.0% at 13 weeks

13 weeks
CGM-measured Time In Tight Range (TITR) 70-140 mg/dL
Lasso di tempo: 13 weeks

CGM-measured time in tight range (TITR) 70-140 mg/dL

13 weeks
CGM-measured Area Over the Curve (70 mg/dL)
Lasso di tempo: 13 weeks

CGM-measured area over the curve (70 mg/dL)

13 weeks
CGM-measured Low Sensor Glucose Events
Lasso di tempo: 13 weeks

CGM-measured low sensor glucose events

13 weeks
CGM-measured Prolonged High Sensor Glucose Events
Lasso di tempo: 13 weeks

CGM-measured prolonged high sensor glucose events

13 weeks
CGM-measured Time >300 mg/dL
Lasso di tempo: 13 weeks

CGM-measured time >300 mg/dL

13 weeks
CGM-measured Area Under the Curve (180 mg/dL)
Lasso di tempo: 13 weeks

CGM-measured area under the curve (180 mg/dL)

13 weeks
CGM-measured TIR >70%
Lasso di tempo: 13 weeks

CGM-measured TIR >70%

13 weeks
CGM-measured TIR Improvement From Baseline To 13 Weeks ≥5%
Lasso di tempo: 13 weeks

CGM-measured TIR improvement from baseline to 13 weeks ≥5%

13 weeks
CGM-measured TIR Improvement From Baseline To 13 Weeks ≥10%
Lasso di tempo: 13 weeks

CGM-measured TIR improvement from baseline to 13 weeks ≥10%

13 weeks
CGM-measured Time <70 mg/dL <4%
Lasso di tempo: 13 weeks

CGM-measured time <70 mg/dL <4%

13 weeks
CGM-measured Time <54 mg/dL <1%
Lasso di tempo: 13 weeks

CGM-measured time <54 mg/dL <1%

13 weeks
CGM-measured TIR >70% and Time <54 mg/dL <1%
Lasso di tempo: 13 weeks

CGM-measured TIR >70% and time <54 mg/dL <1%

13 weeks
CGM-measured Improvement In TIR By >10% Without An Increase In Time <54 mg/dL By >0.5%
Lasso di tempo: 13 weeks

CGM-measured improvement in TIR by >10% without an increase in time <54 mg/dL by >0.5%

13 weeks
Type 1 Diabetes Distress Scale (T1-DDS)
Lasso di tempo: Screening, 13 weeks

The T1-DDS is to evaluate diabetes-related emotional distress in type 1 diabetic patients. The scale consists of 17 items, contains 4 domains (emotional burden subscale, physician-related subscale, regimen-related distress subscale, and diabetes-related interpersonal distress). Each item is rated on a 6-point Likert scale from 1 (no problem) to 6 (serious problem). Patients with higher scores are considered with more distress

Screening, 13 weeks
Problem Areas In Diabetes - Teens (PAID-T) and Parents of Teens (P-PAID-T)
Lasso di tempo: Screening, 13 weeks

The PAID-T and P-PAID-T questionnaires consist of 26 items that are scored on a 6-point Likert scale from 1-2 (not a problem) to 5-6 (serious problem). The derived total score (26 questions) ranges between 26 and 156, where high scores represent a higher burden

Screening, 13 weeks
Hypoglycemia Confidence Scale (≥18)
Lasso di tempo: Screening, 13 weeks

A person-reported outcome measure (PROM) that examines the degree to which people with diabetes feel able, secure, and comfortable regarding their ability to stay safe from hypoglycemic-related problems (9-item scale with 4 choices that range from 1 (Not Confident At All) to 4 (Very Confident)). The total score can range from 1 to 4, with a higher score indicating a better outcome

Screening, 13 weeks
INSPIRE Survey (Insulin Delivery Systems: Perceptions, Ideas, Reflections, and Expectations)
Lasso di tempo: Screening, 13 weeks

INSPIRE 5-point Likert scale from strongly agree to strongly disagree, along with an N/A option

Screening, 13 weeks
Fear of Hypoglycemia Survey (HFS-II) - Total Score, 2 Subscales and 4 Factor Scores
Lasso di tempo: Screening, 13 weeks

Fear of Hypoglycemia Survey (HFS-II) - total score, 2 subscales and 4 factor scores: Behavior (avoidance, maintain high BG), Worry (helplessness, social consequences)

Screening, 13 weeks
The EuroQol 5 Dimension 5 Level (EQ-5D-5L)
Lasso di tempo: Screening, 13 weeks

The EQ-5D-5L is a standardized measure of health status developed by the EuroQol Group in order to provide a simple, generic measure of health for clinical appraisal. The EQ-5D evaluates 5 dimensions (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) using a 5-level severity scale from 1 (no problems) to 5 (extreme problems), and is converted to a single summary index by applying a formula that essentially attaches weight to each of the levels in each dimension. The visual analogue score (VAS) evaluates the health condition assessed by patients to producae a quantitive measure of health outcome that reflects the patient's own judgement on a range from "the worst health you can imagine" to "the best health you can imagine"

Screening, 13 weeks
World Health Organization Well-being Index (WHO-5)
Lasso di tempo: Screening, 13 weeks

WHO-5 is a 5-item questionnaire of the World Health Organization that measures health related quality of life. Each item is scored on a scale of 0 (at no time) to 5 (all the time). Higher scores indicate greater well-being

Screening, 13 weeks
Perceived Benefits and Burdens of AID Systems
Lasso di tempo: Screening, 13 weeks

A 35-item survey that assesses user expectations of a hybrid closed loop AID system using a 5-point Likert scale from "strongly disagree" to "strongly agree"

Screening, 13 weeks
Total Daily Insulin (Units/kg)
Lasso di tempo: 13 weeks

Total daily insulin (Units/kg)

13 weeks
Percentage of Total Insulin Delivered Via Basal
Lasso di tempo: 13 weeks

Percentage of total insulin delivered via basal

13 weeks
Percentage of Total Insulin Delivered Via Bolus
Lasso di tempo: 13 weeks

Percentage of total insulin delivered via bolus

13 weeks
Weight
Lasso di tempo: 13 weeks

Weight

13 weeks
Body Mass Index (BMI)
Lasso di tempo: 13 weeks

Body Mass Index (BMI)

13 weeks
Number of Severe Hypoglycemia (SH) Events and SH Event Rate Per 100 person-years
Lasso di tempo: 13 weeks

Number of Severe Hypoglycemia (SH) events and SH event rate per 100 person-years

13 weeks
Number of Diabetes Ketoacidosis (DKA) Events and DKA Event Rate Per 100 person-years
Lasso di tempo: 13 weeks

Number of Diabetes Ketoacidosis (DKA) events and DKA event rate per 100 person-years

13 weeks
Number of Other Serious Adverse Events (SAEs other than SH events and DKA events)
Lasso di tempo: 13 weeks

Number of Other Serious Adverse Events (SAEs other than SH events and DKA events)

13 weeks
Number of Unanticipated Adverse Device Effects (UADE)
Lasso di tempo: 13 weeks

Number of Unanticipated Adverse Device Effects (UADE)

13 weeks
Number of Infusion Set Failures
Lasso di tempo: 13 weeks

Number of infusion set failures

13 weeks
Other Device Malfunctions/Device Issues
Lasso di tempo: 13 weeks

Number of other malfunctions/issues related to the study device

13 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Cattedra di studio: Melissa Putman, MD, Massachusetts General Hospital
  • Direttore dello studio: Judy Sibayan, MPH, Jaeb Center for Health Research

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

24 settembre 2024

Completamento primario (Stimato)

30 giugno 2027

Completamento dello studio (Stimato)

30 giugno 2027

Date di iscrizione allo studio

Primo inviato

20 maggio 2024

Primo inviato che soddisfa i criteri di controllo qualità

3 giugno 2024

Primo Inserito (Effettivo)

10 giugno 2024

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

9 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

6 novembre 2026

Ultimo verificato

1 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

Sì

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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