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Verapamil Effect in Cystic Fibrosis-related Dysglycemia

7 luglio 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

30

Fase

  • Fase 2

Contatti e Sedi

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

Contatto studio

Luoghi di studio

    • Massachusetts
      • Boston, Massachusetts, Stati Uniti, 02114
        • Diabetes Research Center, Massachusetts General Hospital
        • Contatto:
    • Rhode Island
      • Providence, Rhode Island, Stati Uniti, 02903
        • Rhode Island Hospital
        • Contatto:

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

  • Bambino
  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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

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: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in 30-minute C-peptide area under the curve after mixed-meal tolerance test
Lasso di tempo: Baseline, 6 months
laboratory test, measured in ng/mL
Baseline, 6 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in 180 minute C-peptide area under the curve after mixed-meal tolerance test
Lasso di tempo: 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
Lasso di tempo: Baseline, 6 months
laboratory test, measured in microIU/mL
Baseline, 6 months
Change in proinsulin area under the curve after mixed-meal tolerance test
Lasso di tempo: Baseline, 6 months
laboratory test, measured in pmol/L
Baseline, 6 months
Change in glucose area under the curve after mixed-meal tolerance test
Lasso di tempo: Baseline, 6 months
laboratory test, measured in mg/dL
Baseline, 6 months
Change in hemoglobin A1c
Lasso di tempo: Baseline, 6 months
laboratory test, measured in %
Baseline, 6 months
Change in elexacaftor/tezacaftor/ivacaftor trough levels
Lasso di tempo: Baseline, 8 weeks, 6 months
Laboratory test, measured in micrograms/mL
Baseline, 8 weeks, 6 months
Change in aspartate aminotransferase (AST)
Lasso di tempo: Baseline, 8 weeks, 6 months
Laboratory test, measured in IU/L
Baseline, 8 weeks, 6 months
Change in alanine aminotransferase (ALT)
Lasso di tempo: Baseline, 8 weeks, 6 months
Laboratory test, measured in IU/L
Baseline, 8 weeks, 6 months
Change in glucose management indicator (GMI) %
Lasso di tempo: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in average glucose (AG) mg/dL
Lasso di tempo: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in standard deviation (SD)
Lasso di tempo: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in coefficient of variation (CV)
Lasso di tempo: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time <54 mg/dL
Lasso di tempo: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time <70 mg/dL
Lasso di tempo: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time >180 mg/dL
Lasso di tempo: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time >250 mg/dL
Lasso di tempo: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time 70-180 mg/dL
Lasso di tempo: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in percent time 70-140 mg/dL
Lasso di tempo: Baseline, 8 weeks, 6 months
continuous glucose monitoring
Baseline, 8 weeks, 6 months
Change in Chronic Respiratory Infection Symptom Score (CRISS)
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: Baseline, 8 weeks, 6 months
Pulmonary function will be assessed using spirometry
Baseline, 8 weeks, 6 months
Change in blood pressure
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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

Collaboratori e investigatori

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

Sponsor

Pubblicazioni e link utili

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Pubblicazioni generali

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 (Stimato)

1 agosto 2026

Completamento primario (Stimato)

1 luglio 2028

Completamento dello studio (Stimato)

31 agosto 2028

Date di iscrizione allo studio

Primo inviato

30 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

30 giugno 2026

Primo Inserito (Effettivo)

7 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

9 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

7 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 2390110

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

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

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 .