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NCT Number: NCT06273072

Metformin IN Asthma for Overweight and Obese Individuals (MINA)

This is a randomized clinical trial of metformin among overweight or obese adults with not well-controlled asthma despite maintenance inhaler therapy.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Johns Hopkins University, Baltimore, Maryland, United States

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About this study

This is a randomized, placebo-controlled, parallel-arm pilot clinical trial. Adult participants who are overweight or obese and have not well-controlled asthma despite use of an inhaled corticosteroid will be randomized to metformin, an FDA-approved medication for the treatment of type 2 diabetes mellitus, or to placebo, to be taken daily for a total duration of six months. Recruitment will occur at two sites in the United States.

Randomized participants will have regular telemedicine visits to assess side effects and adherence. Additionally, participants will have a measurement of asthma outcomes at randomization and at 3 and 6 months after randomization.

The purpose of this study is to determine feasibility to inform a future multi-center clinical trial of metformin in this population.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Physician-diagnosed asthma on maintenance therapy
  • Not well-controlled asthma (ACT score <20, or at least one asthma exacerbation requiring corticosteroids in the prior 12 months)
  • Overweight or obesity: Body mass index ≥25kg/m2
  • Adult: Age ≥18

Exclusion criteria

  • Currently pregnant, expect to become pregnant in the next 6 months or are currently breastfeeding
  • Major cardiovascular disease: heart failure, heart attack or stroke within the last 6 months
  • Other chronic lung disease, inclusive of chronic obstructive pulmonary disease, bronchiectasis, interstitial lung disease, pulmonary fibrosis
  • Active smoking or former smoker with ≥20 pack-year smoking history
  • Chronic kidney disease: estimated glomerular filtration rate ≤60 mL/min/1.73 m2
  • Heavy alcohol use: in a typical week, 8 or more drinks for a woman or 15 or more drinks for a man
  • Liver disease: elevation in aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 2x the upper limit of normal or prior diagnosis of liver disease
  • Anemia: hemoglobin < 13 g/dl in males and hemoglobin < 11 g/dl in females
  • Taking Glucagon Like Peptide 1(GLP-1) medications for weight loss
  • Diabetes (Hemoglobin A1C ≥ 6.5% or taking metformin or other medications used to treat diabetes)
  • Participation in any other clinical trial (observational studies are permitted)

Treatment and study plan

Metformin Hydrochloride Extended-Release Tablets

Drug

titrated to 2000 mg once daily

Visually identical placebo Metformin hydrochloride extended-release tablets

Drug

placebo

Primary outcomes

  1. Number of completed telemedicine visits

    Time frame: Baseline to week 24

    Number of participants completing at least 3 out of the 4 monitoring telemedicine visits

  2. Adherence to study drug

    Time frame: Baseline to week 24

    Adherence will be measured by pill count

  3. Retention rate

    Time frame: Baseline to week 24

    Investigators will collect data on the number of subjects screened, randomized, and complete the final in-person visit

Secondary outcomes

  1. Asthma control as assessed by the Asthma Control Test (ACT) score

    Time frame: Baseline to week 24

    Difference in Asthma Control Test (ACT) score at week 24; range is from 5-25 with higher being better asthma control

  2. Change in Asthma exacerbations rate

    Time frame: Baseline to week 24

    Change in (annualized) asthma exacerbations rate at week 24

  3. Pre-bronchodilator lung function

    Time frame: Baseline to week 24

    Difference in volume of air exhaled in the first second during spirometry (FEV1) at week 24

  4. Fractional exhaled nitric oxide (FeNO)

    Time frame: Baseline to week 24

    Difference in FeNO between baseline and week 24

  5. Airways hyperresponsiveness

    Time frame: Baseline to week 24

    Difference in cumulative dose of mannitol required to precipitate a significant decrement in FEV1 between baseline at week 24

Study contacts

Contact information is provided by the study sponsor or research team.

Meredith C McCormack, M.D., M.H.S.

CONTACT

[email protected]

410-550-6205

Rachelle Koehl, M.S.

CONTACT

[email protected]

410-955-1530

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • Baylor College of Medicine
  • National Heart, Lung, and Blood Institute (NHLBI)
  • Temple University

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2028
First posted
Feb 22, 2024
Registry last updated
Jan 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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