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Verapamil Effect in Cystic Fibrosis-related Dysglycemia

2026年7月7日 更新者: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.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (推定)

30

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Massachusetts
      • Boston、Massachusetts、アメリカ、02114
        • Diabetes Research Center, Massachusetts General Hospital
        • コンタクト:
    • Rhode Island
      • Providence、Rhode Island、アメリカ、02903
        • Rhode Island Hospital
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子
  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in 30-minute C-peptide area under the curve after mixed-meal tolerance test
時間枠:Baseline, 6 months
laboratory test, measured in ng/mL
Baseline, 6 months

二次結果の測定

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

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出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

一般刊行物

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年8月1日

一次修了 (推定)

2028年7月1日

研究の完了 (推定)

2028年8月31日

試験登録日

最初に提出

2026年6月30日

QC基準を満たした最初の提出物

2026年6月30日

最初の投稿 (実際)

2026年7月7日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月9日

QC基準を満たした最後の更新が送信されました

2026年7月7日

最終確認日

2026年7月1日

詳しくは

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個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

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米国FDA規制医薬品の研究

はい

米国FDA規制機器製品の研究

いいえ

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