- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07688070
Verapamil Effect in Cystic Fibrosis-related Dysglycemia
The Effect of Verapamil on Beta Cell Function in Adolescents and Adults With Cystic Fibrosis-related Dysglycemia
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
Contacts et emplacements
Coordonnées de l'étude
- Nom: Kevin J Scully
- Numéro de téléphone: 401-444-5504
- E-mail: kevin_scully@brown.edu
Lieux d'étude
-
-
Massachusetts
-
Boston, Massachusetts, États-Unis, 02114
- Diabetes Research Center, Massachusetts General Hospital
-
Contact:
- Melissa Putman
- Numéro de téléphone: 617-726-8722
- E-mail: msputman@mgh.harvard.edu
-
-
Rhode Island
-
Providence, Rhode Island, États-Unis, 02903
- Rhode Island Hospital
-
Contact:
- Kevin J Scully
- Numéro de téléphone: 401-444-5504
- E-mail: kevin_scully@brown.edu
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Age 14 years and older
- Genetically-confirmed diagnosis of cystic fibrosis
- Clinical diagnosis of pancreatic insufficiency, defined as requiring pancreatic enzyme replacement therapy (PERT)
Diagnosis of AGT or CFRD within 3-months of study enrollment
- 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
- CFRD is defined as having a fasting glucose >126 mg/dL and/or OGTT 2-hour glucose >200 mg/dL
- Willing to attempt to maximize verapamil to the goal study dosage of 360 mg PO daily
- If taking elexacaftor/tezacaftor/ivacaftor (ETI), willing to adjust dosing
Exclusion Criteria:
- Severe lung disease indicated by forced expiratory volume in 1 second (FEV1) <50% predicted on most recent spirometry testing
- Body mass index (BMI) <18 kg/m2
- Weight <50 kg
- Current or planned pregnancy within the next 6 months
- Treatment with IV antibiotics for a CF exacerbation within 1 month
- Systemic supraphysiologic glucocorticoid use within 1 month
- Initiation or discontinuation of a CFTR modulator within 3 months (i.e. recent change in CFTR modulator formulation/usage)
- Current use of insulin, a GLP-1 receptor agonist, or oral anti-diabetic agent
- Most recent HbA1c >7%
- Not taking a CFTR modulator due to genotype-ineligibility
- Current use of vanzacaftor/tezacaftor/deutivcaftor
- Known hypersensitivity to verapamil
- Blood pressure (BP) <90/60 (adults) or <5th centile for age and gender (youth) in 2 out of 3 measurements
- Heart rate (HR) <60 bpm (adults) or <2nd centile for age and gender (youth) in 2 out of 3 measurements
- History of previously diagnosed vasovagal syncopal episodes related to hypotension
- History of significant cardiac disease (e.g. severe ventricular dysfunction, hypertrophic cardiomyopathy)
- History of certain arrhythmias (e.g. AV block, accessory pathway such as Wolff-Parkinson-White or Lown-Ganong-Levine syndromes)
- 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
- End stage renal disease on dialysis
- History of Duchenne's muscular dystrophy
- Need for the use of any pertinent medications (beta blockers, carbamazepine, phenobarbital, phenytoin, HMG-CoA reductase inhibitors, lithium, theophylline, clonidine).
- Allergy to any of the components of the MMTT standardized meal
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in 30-minute C-peptide area under the curve after mixed-meal tolerance test
Délai: Baseline, 6 months
|
laboratory test, measured in ng/mL
|
Baseline, 6 months
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in 180 minute C-peptide area under the curve after mixed-meal tolerance test
Délai: 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
Délai: Baseline, 6 months
|
laboratory test, measured in microIU/mL
|
Baseline, 6 months
|
|
Change in proinsulin area under the curve after mixed-meal tolerance test
Délai: Baseline, 6 months
|
laboratory test, measured in pmol/L
|
Baseline, 6 months
|
|
Change in glucose area under the curve after mixed-meal tolerance test
Délai: Baseline, 6 months
|
laboratory test, measured in mg/dL
|
Baseline, 6 months
|
|
Change in hemoglobin A1c
Délai: Baseline, 6 months
|
laboratory test, measured in %
|
Baseline, 6 months
|
|
Change in elexacaftor/tezacaftor/ivacaftor trough levels
Délai: Baseline, 8 weeks, 6 months
|
Laboratory test, measured in micrograms/mL
|
Baseline, 8 weeks, 6 months
|
|
Change in aspartate aminotransferase (AST)
Délai: Baseline, 8 weeks, 6 months
|
Laboratory test, measured in IU/L
|
Baseline, 8 weeks, 6 months
|
|
Change in alanine aminotransferase (ALT)
Délai: Baseline, 8 weeks, 6 months
|
Laboratory test, measured in IU/L
|
Baseline, 8 weeks, 6 months
|
|
Change in glucose management indicator (GMI) %
Délai: Baseline, 8 weeks, 6 months
|
continuous glucose monitoring
|
Baseline, 8 weeks, 6 months
|
|
Change in average glucose (AG) mg/dL
Délai: Baseline, 8 weeks, 6 months
|
continuous glucose monitoring
|
Baseline, 8 weeks, 6 months
|
|
Change in standard deviation (SD)
Délai: Baseline, 8 weeks, 6 months
|
continuous glucose monitoring
|
Baseline, 8 weeks, 6 months
|
|
Change in coefficient of variation (CV)
Délai: Baseline, 8 weeks, 6 months
|
continuous glucose monitoring
|
Baseline, 8 weeks, 6 months
|
|
Change in percent time <54 mg/dL
Délai: Baseline, 8 weeks, 6 months
|
continuous glucose monitoring
|
Baseline, 8 weeks, 6 months
|
|
Change in percent time <70 mg/dL
Délai: Baseline, 8 weeks, 6 months
|
continuous glucose monitoring
|
Baseline, 8 weeks, 6 months
|
|
Change in percent time >180 mg/dL
Délai: Baseline, 8 weeks, 6 months
|
continuous glucose monitoring
|
Baseline, 8 weeks, 6 months
|
|
Change in percent time >250 mg/dL
Délai: Baseline, 8 weeks, 6 months
|
continuous glucose monitoring
|
Baseline, 8 weeks, 6 months
|
|
Change in percent time 70-180 mg/dL
Délai: Baseline, 8 weeks, 6 months
|
continuous glucose monitoring
|
Baseline, 8 weeks, 6 months
|
|
Change in percent time 70-140 mg/dL
Délai: Baseline, 8 weeks, 6 months
|
continuous glucose monitoring
|
Baseline, 8 weeks, 6 months
|
|
Change in Chronic Respiratory Infection Symptom Score (CRISS)
Délai: 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
Délai: 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)
Délai: 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
Délai: 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
Délai: 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)
Délai: 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)
Délai: Baseline, 8 weeks, 6 months
|
Pulmonary function will be assessed using spirometry
|
Baseline, 8 weeks, 6 months
|
|
Change in blood pressure
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
|
Collaborateurs et enquêteurs
Parrainer
Publications et liens utiles
Publications générales
- Norris AW, Ode KL, Merjaneh L, Sanda S, Yi Y, Sun X, Engelhardt JF, Hull RL. Survival in a bad neighborhood: pancreatic islets in cystic fibrosis. J Endocrinol. 2019 Apr;241(1):R35-R50. doi: 10.1530/JOE-18-0468.
- Forlenza GP, McVean J, Beck RW, Bauza C, Bailey R, Buckingham B, DiMeglio LA, Sherr JL, Clements M, Neyman A, Evans-Molina C, Sims EK, Messer LH, Ekhlaspour L, McDonough R, Van Name M, Rojas D, Beasley S, DuBose S, Kollman C, Moran A; CLVer Study Group. Effect of Verapamil on Pancreatic Beta Cell Function in Newly Diagnosed Pediatric Type 1 Diabetes: A Randomized Clinical Trial. JAMA. 2023 Mar 28;329(12):990-999. doi: 10.1001/jama.2023.2064.
- Ntimbane T, Krishnamoorthy P, Huot C, Legault L, Jacob SV, Brunet S, Levy E, Gueraud F, Lands LC, Comte B. Oxidative stress and cystic fibrosis-related diabetes: a pilot study in children. J Cyst Fibros. 2008 Sep;7(5):373-84. doi: 10.1016/j.jcf.2008.01.004. Epub 2008 Apr 16.
- Umashankar B, Eliasson L, Ooi CY, Kim KW, Shaw JAM, Waters SA. Beyond insulin: Unraveling the complex interplay of ER stress, oxidative damage, and CFTR modulation in CFRD. J Cyst Fibros. 2024 Sep;23(5):842-852. doi: 10.1016/j.jcf.2024.06.004. Epub 2024 Jun 18.
- Ode KL, Ballman M, Battezzati A, Brennan A, Chan CL, Hameed S, Ismail HM, Kelly A, Moran AM, Rabasa-Lhoret R, Saxby NA, Craig ME. ISPAD Clinical Practice Consensus Guidelines 2022: Management of cystic fibrosis-related diabetes in children and adolescents. Pediatr Diabetes. 2022 Dec;23(8):1212-1228. doi: 10.1111/pedi.13453. No abstract available.
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Maladies génétiques, innées
- Maladies des voies respiratoires
- Maladies du système digestif
- Maladies pulmonaires
- Nourrisson, nouveau-né, maladies
- Maladies pancréatiques
- Maladies et anomalies congénitales, héréditaires et néonatales
- Fibrose kystique
- Produits chimiques organiques
- Amines
- Phénéthylamines
- Éthylamines
- Vérapamil
Autres numéros d'identification d'étude
- 2390110
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .