Could a diabetes drug tame asthma in obesity? new trial investigates
NCT ID NCT05254314
First seen Jun 27, 2026 · Last updated Sep 18, 2026 · Updated 2 times
Summary
This Phase 2 trial tests whether semaglutide (Wegovy), a drug approved for diabetes and weight loss, can improve asthma control in 100 adults with obesity and persistent asthma despite using inhaled steroids. Participants receive weekly injections of semaglutide or a placebo for up to 24 weeks. The study measures changes in asthma symptoms and airway inflammation to see if the drug has direct benefits beyond weight loss.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Semaglutide (Wegovy) injection
- What this could lead to
- If it works, this could point toward a new treatment option for people with obesity-related asthma that is not well controlled with standard inhalers.
- What could go wrong
- This is a mid-stage trial with only 100 participants, so results may not apply to everyone. Semaglutide can cause side effects like nausea and vomiting, and it is not yet proven to help asthma directly.
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 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2022
- Expected to finish
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Dec 2026
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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18 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. . Subject must be able to understand and provide informed consent. 2. Males and females age 18 or older 3. Obesity defined as body mass index (BMI) \>=30, or \>=27 in the setting of \>=1 weight-related comorbidity: * clinically documented hypertension (\>130 mmHg systolic or \>85 mmHg diastolic or treatment) in the prior year or during run-in * clinically documented dyslipidemia (Triglycerides ш 150 mg/dl, HDL \<40 mg/dl in males or \<50 mg/dl in females, \>=130 mg/dl or treatment) in the prior year or during run-in * current obstructive sleep apnea treatment * documented pre-diabetes defined by A1c 5.7-\<6.5 in the prior year or during run-in * clinically documented cardiovascular disease 4. History of physician-diagnosed asthma 5. Persistent Asthma as determined by the requirement of at least medium-dose daily inhaled corticosteroid or more 6. Symptomatic asthma with an ACQ-6 score \>=1.5 at enrollment and at the time of randomization 7. Patient report of stable asthma controller regimen for the prior 8 weeks 8. Evidence of bronchodilator responsiveness (\>=12% and at least 200 mL increase in FEV1) or airway hyperresponsiveness with a Methacholine PC20 \<=16 mg/mL or PD20 \<=400 mcg in the prior year 9. Female subjects of childbearing potential must have a negative pregnancy test upon study entry 10. Female subjects of childbearing potential must agree to use a highly effective birth control method (e.g. hormonal, surgical or abstinence) for the duration of the study Exclusion Criteria: At enrollment: 1. Inability or unwillingness of a subject to give written informed consent or comply with the study protocol 2. Diagnosis of type I or type II diabetes mellitus (DM) or HbA1c ≥6.5 on screening labs 3. Use of \>8 puffs/inhalations of short-acting bronchodilators most days in the previous week (i.e. answer to question #6 on ACQ-6 = 4, 5, or 6) 4. Oxygen saturation \< 94% on room air 5. Patient-reported Tobacco, e-cigarette, or smoked marijuana use within 12 months#, or \>10 pack-years of use\* * Can still be enrolled if ≥40 years old, smoked \<20 pack years, none within 12 months#, and demonstrate a post-bronchodilator FEV1/FVC ratio of \>0.7 or a DLCO z-score of -1.645 or greater (or the equivalent ≥ 75% of predicted) documented in prior 12 months or during run-in \* Smoking equivalent pack years. One pack of cigarettes a day for 1 year is equivalent to: * 1 cigar or pipe per day for 1 year * Smoked hookah or shisha =1 session per day for 1 year * Vaped e-cigarettes =0.5 mLs e-liquid per day for 1 year, or =1 cartridge/tank/pod per day for 1 year * 1 use of inhaled marijuana per day for 1 year #Use of any inhalant \>1 time weekly in the past year is considered use within 12 months. * Active smoking of conventional tobacco, inhaling of marijuana or other drugs, or vaping of e-cigarettes or vape pods \>1 time per week in the past year. * Any form of tobacco qualifies, such as: 1 cigarette, 1 hookah or shisha sessions, 1 cigar, 1 pipe, etc. * Any electronic (e)-device included: e-cigarette e-cig, mod, vape pen, JUUL, e-cigar, e-hookah, e-pipe, vape pods, etc. * Any form of inhaled marijuana, including smoking marijuana leaves or inhaling THC via e-cigarette or device 6. Pregnancy by urine testing, current lactation, or plans to become pregnant during the study period 7. Pharmaceutical weight loss treatment for \>7 days in the prior 90 days at enrollment 8. Previous surgical weight loss treatment. Can still be enrolled if surgery \> 5 years ago and evidence of stable or increasing weight in the prior 3-12 months. 9. Personal history of pancreatitis as determined by history 10. Personal or family history of medullary thyroid cancer by history or multiple endocrine neoplasia syndrome type 2 11. Personal history of gallstone disease without previous cholecystectomy 12. Personal history of gastroparesis 13. Personal history of hypersensitivity to semaglutide 14. Personal history of hypersensitivity to local amide type (ex. Lidocaine) anesthetics 15. Use of antidiabetic agent, other than metformin, including GLP-1R agonist in the previous 90 days. Metformin is allowed provided the dose has been stable in the 90 days prior to screening and will remain stable for the duration of the trial. 16. Use of systemic glucocorticoids in the past 28 days 17. Use of monoclonal antibody for the treatment of asthma in the past 120 days 18. Myocardial infarction, unstable angina, stroke, or heart failure (NYHA class II) within 1 year by history 19. Patient report and confirmed by review of historical diagnostic testing by study physician of other physician-diagnosed chronic respiratory diseases: COPD, cystic fibrosis, pulmonary hypertension, interstitial lung disease, sarcoidosis, bronchiectasis 20. History of physician-diagnosed immune deficiency. 21. History of physician-diagnosed malignancy (other than excised non-melanoma skin cancer) in the past 5 years. 22. Current uncontrolled hypertension (systolic \>150, diastolic \>90) or untreated hyperthyroidism 23. Current, diagnosed or self-reported drug or alcohol abuse that, in the opinion of the investigator, would interfere with the subject's ability to comply with study requirements. 24. Use of investigational drugs within 20 weeks of participation, other than vaccines and/or treatments for SARS-CoV-2 authorized for emergency use 25. Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the subject's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study. At randomization: 26. Screening creatinine elevation with EGFR\<30 ml/min/1.73 m2 collected at visit 1a 27. Compliance to baseline asthma inhaler therapy of \<80% during run-in, at the time of randomization.
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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.
Contacts and locations
Locations
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Vanderbilt University Medical Center
Nashville, Tennessee, 37203, United States
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