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Verapamil Effect in Cystic Fibrosis-related Dysglycemia

7 lipca 2026 zaktualizowane przez: Kevin Scully, Rhode Island Hospital

The Effect of Verapamil on Beta Cell Function in Adolescents and Adults With Cystic Fibrosis-related Dysglycemia

The investigators are conducting a pilot open-label pre/post interventional trial in adolescents and adults with cystic fibrosis (CF) and abnormal glucose tolerance or early CF-related diabetes mellitus (CFRD) to assess the safety and efficacy of verapamil on beta cell function and dysglycemia.

Przegląd badań

Status

Jeszcze nie rekrutacja

Warunki

Interwencja / Leczenie

Szczegółowy opis

Cystic fibrosis-related diabetes (CFRD) is one of the most common non-pulmonary complications of cystic fibrosis (CF) and is associated with reduced pulmonary function, worse nutritional status, earlier mortality, and impaired quality of life. Dysglycemia in CF typically begins with abnormal glucose tolerance (AGT), characterized by impaired first-phase insulin secretion and postprandial hyperglycemia, and may progress over time to CFRD. Insulin therapy is currently the only recommended treatment for CFRD; however, it adds substantial treatment burden to an already medically complex population. At present, there are no approved therapies targeting beta cell dysfunction or aimed at preventing progression from AGT to CFRD in people with CF.

The pathophysiology of CFRD is increasingly recognized as being driven primarily by beta cell dysfunction rather than complete beta cell destruction. Although insulin secretion is impaired in CF, beta cell mass is relatively preserved compared with type 1 diabetes mellitus (T1D), and residual endogenous insulin production often persists for many years after CFRD diagnosis. Mechanisms contributing to beta cell dysfunction in CF are believed to include oxidative stress, inflammation, endoplasmic reticulum stress, impaired antioxidant defenses, and islet immune dysregulation.

Thioredoxin-interacting protein (TXNIP), a key cellular regulator of oxidative stress, has been implicated in beta cell dysfunction and apoptosis in other forms of diabetes mellitus. Verapamil, a calcium channel blocker commonly used for hypertension and arrhythmias, has been shown to reduce TXNIP expression, decrease inflammatory signaling, and promote beta cell survival. Given the known role of oxidative stress in the CF pancreas and the preservation of residual beta cell function in CFRD, verapamil represents a promising candidate therapy for modifying beta cell dysfunction and improving dysglycemia in CF. However, the effects of verapamil on beta cell function and glucose regulation in people with CF have not previously been studied.

This study is a pilot open-label, pre/post interventional trial designed to evaluate the safety, tolerability, and preliminary efficacy of verapamil in adolescents and adults with CF and AGT or early CFRD not currently treated with insulin therapy. Thirty participants aged 14 years and older with genetically confirmed CF, pancreatic insufficiency, and AGT or early CFRD will be enrolled.

Following screening and confirmation of glycemic status by oral glucose tolerance testing (OGTT), participants will complete a two-week blinded continuous glucose monitoring (CGM) run-in period to establish baseline glycemia. Participants will then undergo a baseline mixed meal tolerance test (MMTT) to assess beta cell function. Verapamil extended release (ER) therapy will be initiated at 120 mg daily and titrated over approximately six weeks to a target dose of 360 mg daily as tolerated. Participants will continue treatment for six months, after which CGM and MMTT assessments will be repeated.

The primary efficacy endpoint is the change from baseline in MMTT-stimulated incremental C-peptide area under the curve (AUC) during the first 30 minutes following mixed meal ingestion, a validated measure of first-phase insulin secretion and beta cell function in CF. Secondary efficacy endpoints include changes in additional MMTT-derived measures of insulin secretion and glucose metabolism, hemoglobin A1c, and CGM-derived measures of dysglycemia including time spent in hyperglycemic and hypoglycemic ranges, average glucose, glucose variability, and coefficient of variation. Safety and tolerability assessments will include monitoring of liver function tests, blood pressure, heart rate, electrocardiograms, pulmonary function tests, weight, hypoglycemia, gastrointestinal symptoms, CFTR modulator levels, adverse events, and medication adherence.

The results of this pilot study will provide important preliminary data regarding the feasibility, safety, and potential efficacy of verapamil as a novel therapeutic strategy targeting beta cell dysfunction in CF-related dysglycemia and will help inform the design of future larger randomized clinical trials.

Typ studiów

Interwencyjne

Zapisy (Szacowany)

30

Faza

  • Faza 2

Kontakty i lokalizacje

Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.

Kontakt w sprawie studiów

Lokalizacje studiów

    • Massachusetts
      • Boston, Massachusetts, Stany Zjednoczone, 02114
        • Diabetes Research Center, Massachusetts General Hospital
        • Kontakt:
    • Rhode Island
      • Providence, Rhode Island, Stany Zjednoczone, 02903

Kryteria uczestnictwa

Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.

Kryteria kwalifikacji

Wiek uprawniający do nauki

  • Dziecko
  • Dorosły
  • Starszy dorosły

Akceptuje zdrowych ochotników

Nie

Opis

Inclusion Criteria:

  1. Age 14 years and older
  2. Genetically-confirmed diagnosis of cystic fibrosis
  3. Clinical diagnosis of pancreatic insufficiency, defined as requiring pancreatic enzyme replacement therapy (PERT)
  4. Diagnosis of AGT or CFRD within 3-months of study enrollment

    1. AGT is defined as having either a OGTT 2-hour glucose >140 mg/dL and <200 mg/dL or OGTT 1-hour glucose >200 mg/dL
    2. CFRD is defined as having a fasting glucose >126 mg/dL and/or OGTT 2-hour glucose >200 mg/dL
  5. Willing to attempt to maximize verapamil to the goal study dosage of 360 mg PO daily
  6. If taking elexacaftor/tezacaftor/ivacaftor (ETI), willing to adjust dosing

Exclusion Criteria:

  1. Severe lung disease indicated by forced expiratory volume in 1 second (FEV1) <50% predicted on most recent spirometry testing
  2. Body mass index (BMI) <18 kg/m2
  3. Weight <50 kg
  4. Current or planned pregnancy within the next 6 months
  5. Treatment with IV antibiotics for a CF exacerbation within 1 month
  6. Systemic supraphysiologic glucocorticoid use within 1 month
  7. Initiation or discontinuation of a CFTR modulator within 3 months (i.e. recent change in CFTR modulator formulation/usage)
  8. Current use of insulin, a GLP-1 receptor agonist, or oral anti-diabetic agent
  9. Most recent HbA1c >7%
  10. Not taking a CFTR modulator due to genotype-ineligibility
  11. Current use of vanzacaftor/tezacaftor/deutivcaftor
  12. Known hypersensitivity to verapamil
  13. Blood pressure (BP) <90/60 (adults) or <5th centile for age and gender (youth) in 2 out of 3 measurements
  14. Heart rate (HR) <60 bpm (adults) or <2nd centile for age and gender (youth) in 2 out of 3 measurements
  15. History of previously diagnosed vasovagal syncopal episodes related to hypotension
  16. History of significant cardiac disease (e.g. severe ventricular dysfunction, hypertrophic cardiomyopathy)
  17. History of certain arrhythmias (e.g. AV block, accessory pathway such as Wolff-Parkinson-White or Lown-Ganong-Levine syndromes)
  18. Abnormal liver function tests defined as AST or ALT >1.5 upper limit of normal [ULN] at the time of screening, or end stage cirrhosis
  19. End stage renal disease on dialysis
  20. History of Duchenne's muscular dystrophy
  21. Need for the use of any pertinent medications (beta blockers, carbamazepine, phenobarbital, phenytoin, HMG-CoA reductase inhibitors, lithium, theophylline, clonidine).
  22. Allergy to any of the components of the MMTT standardized meal

Plan studiów

Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.

Jak projektuje się badanie?

Szczegóły projektu

  • Główny cel: Leczenie
  • Przydział: Nie dotyczy
  • Model interwencyjny: Zadanie dla jednej grupy
  • Maskowanie: Brak (otwarta etykieta)

Broń i interwencje

Grupa uczestników / Arm
Interwencja / Leczenie
Eksperymentalny: Intervention Arm
verapamil hydrochloride
Verapamil extended release (ER) will be initiated at a dose of 120mg daily and up-titrated over six weeks to target dose of 360mg daily as tolerated.

Co mierzy badanie?

Podstawowe miary wyniku

Miara wyniku
Opis środka
Ramy czasowe
Change in 30-minute C-peptide area under the curve after mixed-meal tolerance test
Ramy czasowe: Baseline, 6 months
laboratory test, measured in ng/mL
Baseline, 6 months

Miary wyników drugorzędnych

Miara wyniku
Opis środka
Ramy czasowe
Change in 180 minute C-peptide area under the curve after mixed-meal tolerance test
Ramy czasowe: Baseline, 6 months
laboratory test, measured in ng/mL
Baseline, 6 months
Change in insulin level area under the curve after mixed-meal tolerance test
Ramy czasowe: Baseline, 6 months
laboratory test, measured in microIU/mL
Baseline, 6 months
Change in proinsulin area under the curve after mixed-meal tolerance test
Ramy czasowe: Baseline, 6 months
laboratory test, measured in pmol/L
Baseline, 6 months
Change in glucose area under the curve after mixed-meal tolerance test
Ramy czasowe: Baseline, 6 months
laboratory test, measured in mg/dL
Baseline, 6 months
Change in hemoglobin A1c
Ramy czasowe: Baseline, 6 months
laboratory test, measured in %
Baseline, 6 months
Change in elexacaftor/tezacaftor/ivacaftor trough levels
Ramy czasowe: Baseline, 8 weeks, 6 months
Laboratory test, measured in micrograms/mL
Baseline, 8 weeks, 6 months
Change in aspartate aminotransferase (AST)
Ramy czasowe: Baseline, 8 weeks, 6 months
Laboratory test, measured in IU/L
Baseline, 8 weeks, 6 months
Change in alanine aminotransferase (ALT)
Ramy czasowe: Baseline, 8 weeks, 6 months
Laboratory test, measured in IU/L
Baseline, 8 weeks, 6 months
Change in glucose management indicator (GMI) %
Ramy czasowe: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in average glucose (AG) mg/dL
Ramy czasowe: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in standard deviation (SD)
Ramy czasowe: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in coefficient of variation (CV)
Ramy czasowe: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time <54 mg/dL
Ramy czasowe: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time <70 mg/dL
Ramy czasowe: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time >180 mg/dL
Ramy czasowe: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time >250 mg/dL
Ramy czasowe: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time 70-180 mg/dL
Ramy czasowe: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time 70-140 mg/dL
Ramy czasowe: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in Chronic Respiratory Infection Symptom Score (CRISS)
Ramy czasowe: Baseline, 8 weeks, 6 months
8-item patient-reported questionnaire scored from 0 to 100, with higher scores indicating greater symptom severity
Baseline, 8 weeks, 6 months
Change in Patient Assessment of Constipation (PAC) questionnaire score
Ramy czasowe: Baseline, 8 weeks, 6 months
Likert scale questionnaire with 12 items, each scored 0-4, total score ranging from 0-48 with higher scores related to worse outcomes
Baseline, 8 weeks, 6 months
Change in hypoglycemia symptom questionnaire (HSQ)
Ramy czasowe: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (weeks 12, 16, 20), 6 months
5-item patient-reported questionnaire scored from 0-16, with higher scores indicating greater symptom severity
Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (weeks 12, 16, 20), 6 months
Change in Electrocardiogram (ECG)-Measured PR Interval
Ramy czasowe: Baseline, 8 weeks, 6 months
Cardiac conduction assessed by 12-lead electrocardiogram, measured in milliseconds
Baseline, 8 weeks, 6 months
Change in Electrocardiogram (ECG)-Measured QTc Interval
Ramy czasowe: Baseline, 8 weeks, 6 months
Cardiac conduction assessed by 12-lead electrocardiogram, measured in milliseconds
Baseline, 8 weeks, 6 months
Change in percent predicted Forced Expiratory Volume in 1 Second (FEV1)
Ramy czasowe: Baseline, 8 weeks, 6 months
Pulmonary function will be assessed using spirometry
Baseline, 8 weeks, 6 months
Change in percent predicted Forced Vital Capacity (FVC)
Ramy czasowe: Baseline, 8 weeks, 6 months
Pulmonary function will be assessed using spirometry
Baseline, 8 weeks, 6 months
Change in blood pressure
Ramy czasowe: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (week 12, 16, 20), 6 months
electronic cuff measured systolic and diastolic blood pressure, measured in mmHg
Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (week 12, 16, 20), 6 months
Change in heart rate
Ramy czasowe: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (week 12, 16, 20), 6 months
Electronically measured, reported in beats per minute
Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (week 12, 16, 20), 6 months
Change in weight
Ramy czasowe: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (week 12, 16, 20), 6 months
in-perrson and home-reported measurements using study provided scale, measured in kg
Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (week 12, 16, 20), 6 months
Change in body mass index
Ramy czasowe: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (weeks 12, 16, 20), 6 months
in-person and self reported BMI, calculated using study-provided home scale and height on file at baseline
Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (weeks 12, 16, 20), 6 months
Medication Adherence by Pill Count
Ramy czasowe: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (weeks 12, 16, 20), 6 months
Adherence to study medication will be assessed by pill count at study visits. Adherence will be reported as the percentage of prescribed doses taken during the study period.
Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (weeks 12, 16, 20), 6 months

Współpracownicy i badacze

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Sponsor

Publikacje i pomocne linki

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Publikacje ogólne

Daty zapisu na studia

Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.

Główne daty studiów

Rozpoczęcie studiów (Szacowany)

1 sierpnia 2026

Zakończenie podstawowe (Szacowany)

1 lipca 2028

Ukończenie studiów (Szacowany)

31 sierpnia 2028

Daty rejestracji na studia

Pierwszy przesłany

30 czerwca 2026

Pierwszy przesłany, który spełnia kryteria kontroli jakości

30 czerwca 2026

Pierwszy wysłany (Rzeczywisty)

7 lipca 2026

Aktualizacje rekordów badań

Ostatnia wysłana aktualizacja (Rzeczywisty)

9 lipca 2026

Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości

7 lipca 2026

Ostatnia weryfikacja

1 lipca 2026

Więcej informacji

Terminy związane z tym badaniem

Inne numery identyfikacyjne badania

  • 2390110

Plan dla danych uczestnika indywidualnego (IPD)

Planujesz udostępniać dane poszczególnych uczestników (IPD)?

NIE

Informacje o lekach i urządzeniach, dokumenty badawcze

Bada produkt leczniczy regulowany przez amerykańską FDA

Tak

Bada produkt urządzenia regulowany przez amerykańską FDA

Nie

Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .