Cystic Fibrosis Related DiabetesPhase 2NCT07688070
Verapamil Effect in Cystic Fibrosis-related Dysglycemia
A Phase 2 study testing Verapamil Hydrochloride in people with Cystic Fibrosis Related Diabetes and Cystic Fibrosis (CF), run by Rhode Island Hospital at 2 sites in United States.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 14 years and older
- Conditions the study is for
- Cystic Fibrosis Related Diabetes, Cystic Fibrosis (CF), Abnormal Glucose Tolerance
- What is being tested?
- Verapamil Hydrochloride
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 2 sitesUnited States
- Study dates
- 1 Aug 2026to 31 Aug 2028
- Phase
- Phase 2
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 14 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- 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
Who cannot join
- 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
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- 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
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
United States2 sites
Diabetes Research Center, Massachusetts General Hospital
Boston, Massachusetts, 02114
Melissa Putman, 617-726-8722, msputman@mgh.harvard.edu
Rhode Island Hospital
Providence, Rhode Island, 02903
Kevin J Scully, 401-444-5504, kevin_scully@brown.edu
About this study
Official title: 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.
Read the detailed description
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.
- Being tested
- Verapamil Hydrochloride
- Keywords
- cystic fibrosis related diabetes, mixed meal tolerance test, verapamil, beta cell function, continuous glucose monitoring, abnormal glucose tolerance, cystic fibrosis
- Medical subject headings
- Cystic Fibrosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Verapamil HydrochlorideDrug
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.
| Study group | Role | What they receive |
|---|---|---|
| Intervention Arm | Experimental | verapamil hydrochloride Receives: Drug: Verapamil Hydrochloride |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in 30-minute C-peptide area under the curve after mixed-meal tolerance test
laboratory test, measured in ng/mL
Measured: Baseline, 6 months
Secondary outcomes (30)
Change in 180 minute C-peptide area under the curve after mixed-meal tolerance test
laboratory test, measured in ng/mL
Measured: Baseline, 6 months
Change in insulin level area under the curve after mixed-meal tolerance test
laboratory test, measured in microIU/mL
Measured: Baseline, 6 months
Change in proinsulin area under the curve after mixed-meal tolerance test
laboratory test, measured in pmol/L
Measured: Baseline, 6 months
Change in glucose area under the curve after mixed-meal tolerance test
laboratory test, measured in mg/dL
Measured: Baseline, 6 months
Change in hemoglobin A1c
laboratory test, measured in %
Measured: Baseline, 6 months
Change in elexacaftor/tezacaftor/ivacaftor trough levels
Laboratory test, measured in micrograms/mL
Measured: Baseline, 8 weeks, 6 months
Change in aspartate aminotransferase (AST)
Laboratory test, measured in IU/L
Measured: Baseline, 8 weeks, 6 months
Change in alanine aminotransferase (ALT)
Laboratory test, measured in IU/L
Measured: Baseline, 8 weeks, 6 months
Change in glucose management indicator (GMI) %
continuous glucose monitoring
Measured: Baseline, 8 weeks, 6 months
Change in average glucose (AG) mg/dL
continuous glucose monitoring
Measured: Baseline, 8 weeks, 6 months
Change in standard deviation (SD)
continuous glucose monitoring
Measured: Baseline, 8 weeks, 6 months
Change in coefficient of variation (CV)
continuous glucose monitoring
Measured: Baseline, 8 weeks, 6 months
Change in percent time <54 mg/dL
continuous glucose monitoring
Measured: Baseline, 8 weeks, 6 months
Change in percent time <70 mg/dL
continuous glucose monitoring
Measured: Baseline, 8 weeks, 6 months
Change in percent time >180 mg/dL
continuous glucose monitoring
Measured: Baseline, 8 weeks, 6 months
Change in percent time >250 mg/dL
continuous glucose monitoring
Measured: Baseline, 8 weeks, 6 months
Change in percent time 70-180 mg/dL
continuous glucose monitoring
Measured: Baseline, 8 weeks, 6 months
Change in percent time 70-140 mg/dL
continuous glucose monitoring
Measured: Baseline, 8 weeks, 6 months
Change in Chronic Respiratory Infection Symptom Score (CRISS)
8-item patient-reported questionnaire scored from 0 to 100, with higher scores indicating greater symptom severity
Measured: Baseline, 8 weeks, 6 months
Change in Patient Assessment of Constipation (PAC) questionnaire score
Likert scale questionnaire with 12 items, each scored 0-4, total score ranging from 0-48 with higher scores related to worse outcomes
Measured: Baseline, 8 weeks, 6 months
Change in hypoglycemia symptom questionnaire (HSQ)
5-item patient-reported questionnaire scored from 0-16, with higher scores indicating greater symptom severity
Measured: 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
Cardiac conduction assessed by 12-lead electrocardiogram, measured in milliseconds
Measured: Baseline, 8 weeks, 6 months
Change in Electrocardiogram (ECG)-Measured QTc Interval
Cardiac conduction assessed by 12-lead electrocardiogram, measured in milliseconds
Measured: Baseline, 8 weeks, 6 months
Change in percent predicted Forced Expiratory Volume in 1 Second (FEV1)
Pulmonary function will be assessed using spirometry
Measured: Baseline, 8 weeks, 6 months
Change in percent predicted Forced Vital Capacity (FVC)
Pulmonary function will be assessed using spirometry
Measured: Baseline, 8 weeks, 6 months
Change in blood pressure
electronic cuff measured systolic and diastolic blood pressure, measured in mmHg
Measured: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (week 12, 16, 20), 6 months
Change in heart rate
Electronically measured, reported in beats per minute
Measured: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (week 12, 16, 20), 6 months
Change in weight
in-perrson and home-reported measurements using study provided scale, measured in kg
Measured: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (week 12, 16, 20), 6 months
Change in body mass index
in-person and self reported BMI, calculated using study-provided home scale and height on file at baseline
Measured: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (weeks 12, 16, 20), 6 months
Medication Adherence by Pill Count
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.
Measured: Baseline, weekly telehealth visits (weeks 1-7), 8 weeks, monthly telehealth visits (weeks 12, 16, 20), 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Jul 2026
- Study start1 Aug 2026 (estimated)
- Primary completion1 Jul 2028 (estimated)
- Study completion31 Aug 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (5)Papers the sponsor has linked to this study.
- Other trials for Cystic Fibrosis Related DiabetesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Pre/post interventional trial
- Masking
- None (open label)
- Enrolment
- 30 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Rhode Island Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Kevin Scully, Rhode Island Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07688070
- Sponsor's protocol ID
- 2390110
- Status last verified
- Jul 2026
- First submitted
- 30 Jun 2026
- Last updated
- 9 Jul 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
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.
PubMed 36826844Ntimbane 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.
PubMed 18420468Umashankar 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.
PubMed 38897882Ode 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.
PubMed 36537525Norris 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.
PubMed 30759072