Blood pressure drug may help preserve insulin in cystic fibrosis
NCT ID NCT07688070
First seen Jul 07, 2026 · Last updated Jul 10, 2026 · Updated 3 times
Summary
This study tests whether verapamil, a common blood pressure medication, can help protect insulin-producing cells in people with cystic fibrosis who have early blood sugar problems or diabetes. Participants take verapamil for several weeks, and researchers measure changes in insulin and C-peptide levels after a meal. The goal is to see if this drug can slow or improve glucose control in this population.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- verapamil (a blood pressure medication)
- What this could lead to
- If it works, this could point toward a new way to preserve insulin production and manage blood sugar in people with cystic fibrosis.
- What could go wrong
- This is a small, early pilot study without a placebo group, so results may not be conclusive. Verapamil can cause side effects like low blood pressure or constipation.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Aug 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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14 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Diabetes Research Center, Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
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Rhode Island Hospital
Providence, Rhode Island, 02903, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A low-intervention prospective-retrospective study to evaluate the pharmacokinetics of Elexacaftor/Tezacaftor/Ivacaftor combination in a cystic fibrosis population
- MRI could reveal a new way to ease gut troubles in cystic fibrosis
- AI may predict lung decline in cystic fibrosis kids using muscle and balance data
- Breathing vs. beating: which technique clears lungs better in cystic fibrosis?
- Could modern CF drugs make daily inhaled treatments obsolete?
- New study investigates hidden heart risks in cystic fibrosis patients on modern drugs