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Verapamil Effect in Cystic Fibrosis-related Dysglycemia

7. juli 2026 oppdatert av: 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.

Studieoversikt

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Antatt)

30

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Massachusetts
      • Boston, Massachusetts, Forente stater, 02114
        • Diabetes Research Center, Massachusetts General Hospital
        • Ta kontakt med:
    • Rhode Island
      • Providence, Rhode Island, Forente stater, 02903
        • Rhode Island Hospital
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in 30-minute C-peptide area under the curve after mixed-meal tolerance test
Tidsramme: Baseline, 6 months
laboratory test, measured in ng/mL
Baseline, 6 months

Sekundære resultatmål

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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. august 2026

Primær fullføring (Antatt)

1. juli 2028

Studiet fullført (Antatt)

31. august 2028

Datoer for studieregistrering

Først innsendt

30. juni 2026

Først innsendt som oppfylte QC-kriteriene

30. juni 2026

Først lagt ut (Faktiske)

7. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

9. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

7. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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