Blood pressure drug may help preserve insulin in cystic fibrosis

NCT ID NCT07688070

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

About 30 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Aug 2026

An estimate. Start dates often move.

Expected to finish

Aug 2028

An estimate. End dates often move.

Lead sponsor

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

14 years and older

Sex

Anyone

Healthy volunteers

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

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.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Diabetes Research Center, Massachusetts General Hospital

    Boston, Massachusetts, 02114, United States

  • Rhode Island Hospital

    Providence, Rhode Island, 02903, United States

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