COPDPhase 2GLIMR COPDNCT07747805
GLP-1 Agonists for Lung Function Improvement and Muscle Restoration in COPD
A Phase 2 study testing Tirzepatide in people with COPD and Obesity & Overweight, run by The Cleveland Clinic at 1 site in United States.
Trial summary
Chronic obstructive pulmonary disease (COPD) is associated with systemic inflammation, obesity-related metabolic dysfunction, skeletal muscle impairment, and progressive decline in lung function. Read more about this study
- Who is it for?
- Ages 40 to 80 years
- Conditions the study is for
- COPD, Obesity & Overweight, Sarcopenia
- What is being tested?
- Tirzepatide
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 1 siteUnited States
- Study dates
- 28 Aug 2026to 15 Aug 2029
- Phase
- Phase 2
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age 40-80 years
- Diagnosis of chronic obstructive pulmonary disease (COPD) with post-bronchodilator FEV₁/FVC < 0.70
- GOLD stage 1-3 COPD (FEV₁ >30% predicted)
- Former smoker with a smoking history of at least 10 pack-years
- Body mass index (BMI) ≥27 kg/m² with at least one weight-related comorbidity (e.g., prediabetes, hypertension, dyslipidemia, obstructive sleep apnea, or cardiovascular disease) or BMI 30-40 kg/m²
- Able and willing to provide written informed consent
- Able to comply with study procedures and follow-up visits
Who cannot join
- Type 2 diabetes mellitus (HbA1c > 6.5%)
- Pregnancy or breastfeeding
- Coagulopathy, defined as INR > 1.4 or platelet count <80,000/μL
- Active malignancy, including lung cancer
- Use of medications known to significantly alter muscle protein metabolism within 6 weeks of enrollment (e.g., oral corticosteroids, tamoxifen, high-dose estrogen, testosterone)
- Personal or family history of medullary thyroid carcinoma
Show all 17Show fewer
- Multiple endocrine neoplasia syndrome type 2 (MEN2)
- Known hypersensitivity or contraindication to tirzepatide or its components
- History of pancreatitis
- Severe gastrointestinal disease that, in the opinion of the investigator, would increase risk from study participation
- Significant diabetic retinopathy
- Clinically significant renal impairment
- Clinically significant gallbladder disease
- Current treatment with a DPP-4 inhibitor
- COPD exacerbation within 60 days prior to enrollment
- Participation in pulmonary rehabilitation within 2 weeks prior to enrollment
- Any medical, psychiatric, or social condition that, in the opinion of the investigators, may interfere with study participation, adherence to study procedures, or participant safety
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site
Cleveland Clinic
Cleveland, Ohio, 44195
Amy Attaway, MD, 2164452807, attawaa@ccf.org
About this study
Official title: GLIMR COPD: GLP-1 Agonists for Lung Function Improvement and Muscle Restoration in COPD
Chronic obstructive pulmonary disease (COPD) is associated with systemic inflammation, obesity-related metabolic dysfunction, skeletal muscle impairment, and progressive decline in lung function. While obesity has historically been viewed as protective in COPD, emerging evidence suggests that excess adiposity and adipokine dysregulation, particularly elevated leptin levels, contribute to chronic inflammation, impaired muscle function, and worse clinical outcomes. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have demonstrated anti-inflammatory, metabolic, and potential muscle-preserving effects beyond weight loss, making them promising therapeutic candidates for COPD.
The GLIMR COPD study is a prospective, randomized, controlled pilot trial designed to evaluate the effects of tirzepatide on lung function, skeletal muscle health, inflammation, and body composition in overweight and obese adults with COPD. Thirty participants will be enrolled at the Cleveland Clinic COPD Center, including 20 participants receiving tirzepatide and 10 age- and sex-matched control participants. Study participants will be followed for 12 months with assessments performed at screening, baseline, 6 months, and 12 months. Tirzepatide-treated participants will undergo standard dose escalation to a maintenance dose of 2.4 mg weekly.
Read more
The primary objective is to determine the effect of GLP-1 receptor agonist therapy on skeletal muscle function and physiology over 12 months. Secondary objectives include evaluating changes in body composition, systemic inflammation, adipokine signaling, immune function, pulmonary physiology, physical performance, and treatment tolerability.
The study is built around three mechanistic aims. First, we will characterize the effects of GLP-1 therapy on systemic inflammation and immune dysregulation using longitudinal blood-based proteomic analyses and adipokine measurements, including leptin and adiponectin. Second, we will investigate the impact of GLP-1 therapy on skeletal muscle mitochondrial function and fatty acid oxidation using muscle biopsies obtained at baseline and 12 months, combined with high-resolution respirometry, transcriptomics, metabolomics, and proteomics. Third, we will assess changes in clinical outcomes including lung function, body composition, muscle strength, and physical performance.
Participants will undergo comprehensive phenotyping that includes spirometry, respiratory muscle strength testing, six-minute walk testing, handgrip strength, sit-to-stand testing, body composition assessment, diaphragm ultrasound, and non-contrast CT imaging of the lungs and thighs. Blood samples will be collected for biomarker, proteomic, metabolomic, genomic, and immunologic analyses. Vastus lateralis muscle biopsies will be performed at baseline and study completion to evaluate mitochondrial bioenergetics and molecular pathways associated with muscle remodeling.
Eligible participants will be adults aged 40-80 years with COPD, a smoking history of at least 10 pack-years, and overweight or obesity. Individuals with diabetes, active malignancy, recent COPD exacerbations, contraindications to tirzepatide, or conditions that could interfere with study participation will be excluded.
This pilot study is designed to generate critical mechanistic and clinical data regarding the role of GLP-1 receptor agonists in COPD. Findings will help define the relationships among obesity, adipokine signaling, systemic inflammation, skeletal muscle dysfunction, and lung disease progression, while providing preliminary efficacy estimates to support the design of a future multicenter randomized clinical trial evaluating GLP-1 therapy as a novel treatment strategy for COPD.
Read the detailed description
Chronic obstructive pulmonary disease (COPD) is a leading cause of morbidity and mortality worldwide and is increasingly recognized as a systemic disease that affects far more than the lungs. In addition to airflow limitation, many individuals with COPD experience chronic inflammation, loss of skeletal muscle function, reduced exercise capacity, and metabolic abnormalities that contribute substantially to disability, hospitalizations, and reduced quality of life. Obesity, which is highly prevalent among patients with COPD, further worsens these systemic manifestations through complex interactions involving inflammation, altered hormone signaling, and impaired energy metabolism. Despite the significant burden imposed by these metabolic and musculoskeletal complications, few therapies specifically target the underlying biological pathways that connect obesity, inflammation, muscle dysfunction, and lung disease.
The GLIMR COPD study is a randomized, controlled pilot clinical trial designed to investigate whether treatment with the GLP-1/GIP receptor agonist tirzepatide can improve lung function, skeletal muscle health, physical performance, and systemic inflammation in overweight and obese individuals with COPD. Beyond its established effects on weight reduction and glucose regulation, tirzepatide has demonstrated potent anti-inflammatory and metabolic benefits that may favorably influence multiple biological pathways involved in COPD progression. Emerging evidence suggests that GLP-1-based therapies can reduce inflammatory signaling, improve mitochondrial function, enhance skeletal muscle metabolism, and alter adipokine profiles, including reductions in circulating leptin, a hormone that has been strongly associated with worse COPD outcomes.
The study will enroll 30 participants with COPD, including 20 individuals receiving tirzepatide and 10 age- and sex-matched control participants. Participants will undergo detailed evaluations at baseline, six months, and twelve months. These assessments will include pulmonary function testing, exercise capacity measurements, muscle strength testing, body composition analysis, imaging studies, blood biomarker analyses, and skeletal muscle biopsies. By combining clinical assessments with advanced molecular analyses, the study seeks to understand not only whether tirzepatide improves health outcomes, but also the biological mechanisms responsible for those improvements.
The first objective of the study is to determine how tirzepatide influences systemic inflammation and immune dysfunction in COPD. Blood samples collected throughout the study will undergo comprehensive proteomic and biomarker analyses to identify changes in inflammatory pathways and circulating mediators associated with treatment. Particular attention will be given to adipokines such as leptin and adiponectin, which may serve as important links between obesity and COPD progression.
The second objective is to investigate the effects of tirzepatide on skeletal muscle health. Skeletal muscle dysfunction is a major contributor to exercise intolerance and reduced quality of life in COPD. Muscle biopsies obtained before and after treatment will be used to evaluate mitochondrial function, fatty acid oxidation, gene expression, protein signaling, and metabolic pathways that regulate muscle performance and adaptation. These studies will provide important insights into whether tirzepatide directly improves muscle bioenergetics and cellular health.
The third objective is to quantify the effects of tirzepatide on clinically meaningful outcomes. Investigators will assess changes in lung function, respiratory muscle strength, exercise capacity, muscle strength, physical performance, and body composition. Advanced CT imaging will be used to measure changes in skeletal muscle mass, visceral fat, and other body composition characteristics. These measurements will help determine whether improvements in metabolic health translate into better physical function and pulmonary outcomes.
Participants eligible for enrollment will be adults aged 40-80 years with COPD and overweight or obesity. The study is being conducted through the Cleveland Clinic COPD Center, which follows more than 2,500 patients and has extensive experience in COPD clinical research and translational investigations.
The long-term goal of this project is to establish a scientific foundation for larger multicenter clinical trials evaluating incretin-based therapies as novel treatment strategies for COPD. By examining the interconnected relationships among obesity, inflammation, skeletal muscle dysfunction, and lung disease, this study has the potential to identify new therapeutic approaches that address both pulmonary and systemic manifestations of COPD. The findings may ultimately help improve physical function, quality of life, and long-term outcomes for millions of individuals living with COPD.
- Conditions
- COPD, Obesity & Overweight, Sarcopenia
- Being tested
- Tirzepatide
- Keywords
- COPD, sarcopenia, obesity
- Medical subject headings
- Pulmonary Disease, Chronic Obstructive, Obesity, Overweight, Sarcopenia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
TirzepatideDrug
Tirzepatide is a once-weekly subcutaneous dual GIP/GLP-1 receptor agonist administered for 52 weeks using standard dose escalation as tolerated in addition to standard clinical care.
| Study group | Role | What they receive |
|---|---|---|
| COPD control | No intervention | Participants with COPD and overweight or obesity who will not receive tirzepatide and will continue standard clinical care. Participants will complete the same research assessments as the intervention group, including blood collection, pulmonary function testing, physical performance testing, body composition assessments, imaging, and skeletal muscle biopsies, allowing comparison of clinical and biological changes over 12 months. |
| COPD tirzepatide treatment | Active comparator | Participants with COPD and overweight or obesity will receive once-weekly subcutaneous tirzepatide for 52 weeks in addition to standard clinical care. Participants will undergo longitudinal assessments of lung function, skeletal muscle health, body composition, physical performance, and inflammatory biomarkers to evaluate the effects of tirzepatide on pulmonary and systemic manifestations of COPD. Receives: Drug: Tirzepatide |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in FEV1
Change in post-bronchodilator forced expiratory volume in one second (FEV₁) measured by standardized spirometry. FEV₁ will be compared between participants receiving tirzepatide and control participants.
Measured: 12 months
Secondary outcomes (6)
Change in Hand Grip Strength
Change in dominant hand grip strength measured using a calibrated hand dynamometer.
Measured: 6 months and 12 months
Change in Six-Minute Walk Distance (6MWD)
Change in time required to complete five chair rises as a measure of lower extremity muscle function and mobility.
Measured: 6 months and 12 months
Change in Five Sit-to-Stand Performance
Change in time required to complete five chair rises as a measure of lower extremity muscle function and mobility.
Measured: 6 months and 12 months
Change in Lean Muscle Mass
Change in skeletal muscle mass quantified by CT imaging and bioimpedance analysis.
Measured: 12 months
Change in Serum Leptin Concentration
Change in circulating leptin concentration measured from fasting blood samples.
Measured: 6 months and 12 months
Change in Skeletal Muscle Mitochondrial function
Change in mitochondrial respiratory capacity measured in vastus lateralis muscle biopsy specimens.
Measured: 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Aug 2026
- Study start28 Aug 2026 (estimated)
- Primary completion15 Aug 2028 (estimated)
- Study completion15 Aug 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for COPDStudies of the same condition, open and under way.
- More trials run by The Cleveland ClinicThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 30 participants (estimated)
Sponsor and investigators
- Lead sponsor
- The Cleveland Clinic
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Amy Attaway, The Cleveland Clinic
- Investigators
- Amy Attaway, MD, Principal investigator, The Cleveland Clinic
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07747805
- Sponsor's protocol ID
- IRB 25-1092
- Other IDs
- Mandel MAG0024
- Acronym
- GLIMR COPD
- Status last verified
- Jul 2026
- First submitted
- 31 Jul 2026
- Last updated
- 5 Aug 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No: There is no current plan to share individual participant data outside the study team. Any future data sharing will be considered in accordance with participant consent, institutional policies, and regulatory requirements.
Publications
Hong Y, Lee JH, Jeong KW, Choi CS, Jun HS. Amelioration of muscle wasting by glucagon-like peptide-1 receptor agonist in muscle atrophy. J Cachexia Sarcopenia Muscle. 2019 Aug;10(4):903-918. doi: 10.1002/jcsm.12434. Epub 2019 Apr 24.
PubMed 31020810Foer D, Strasser ZH, Cui J, Cahill KN, Boyce JA, Murphy SN, Karlson EW. Association of GLP-1 Receptor Agonists with Chronic Obstructive Pulmonary Disease Exacerbations among Patients with Type 2 Diabetes. Am J Respir Crit Care Med. 2023 Nov 15;208(10):1088-1100. doi: 10.1164/rccm.202303-0491OC.
PubMed 37647574
Study at a glance
From the registry record, last updated by the sponsor on 5 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- GLIMR COPD: GLP-1 Agonists for Lung Function Improvement and Muscle Restoration in COPD
- ClinicalTrials.gov ID
- NCT07747805
- Acronym / sponsor ID
- GLIMR COPD / IRB 25-1092
- Conditions
- COPD, Obesity & Overweight, Sarcopenia
- Keywords
- COPD, sarcopenia, obesity
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 30 participants (estimated)
- Lead sponsor
- The Cleveland ClinicUniversity, hospital or other
- Study start
- 28 Aug 2026 (estimated)
- Primary completion
- 15 Aug 2028 (estimated)
- Study completion
- 15 Aug 2029 (estimated)
- First posted
- 5 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Chronic obstructive pulmonary disease (COPD) is associated with systemic inflammation, obesity-related metabolic dysfunction, skeletal muscle impairment, and progressive decline in lung function. While obesity has historically been viewed as protective in COPD, emerging evidence suggests that excess adiposity and adipokine dysregulation, particularly elevated leptin levels, contribute to chronic inflammation, impaired muscle function, and worse clinical outcomes. Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have demonstrated anti-inflammatory, metabolic, and potential muscle-preserving effects beyond weight loss, making them promising therapeutic candidates for COPD.
The GLIMR COPD study is a prospective, randomized, controlled pilot trial designed to evaluate the effects of tirzepatide on lung function, skeletal muscle health, inflammation, and body composition in overweight and obese adults with COPD. Thirty participants will be enrolled at the Cleveland Clinic COPD Center, including 20 participants receiving tirzepatide and 10 age- and sex-matched control participants. Study participants will be followed for 12 months with assessments performed at screening, baseline, 6 months, and 12 months. Tirzepatide-treated participants will undergo standard dose escalation to a maintenance dose of 2.4 mg weekly.
The primary objective is to determine the effect of GLP-1 receptor agonist therapy on skeletal muscle function and physiology over 12 months. Secondary objectives include evaluating changes in body composition, systemic inflammation, adipokine signaling, immune function, pulmonary physiology, physical performance, and treatment tolerability.
The study is built around three mechanistic aims. First, we will characterize the effects of GLP-1 therapy on systemic inflammation and immune dysregulation using longitudinal blood-based proteomic analyses and adipokine measurements, including leptin and adiponectin. Second, we will investigate the impact of GLP-1 therapy on skeletal muscle mitochondrial function and fatty acid oxidation using muscle biopsies obtained at baseline and 12 months, combined with high-resolution respirometry, transcriptomics, metabolomics, and proteomics. Third, we will assess changes in clinical outcomes including lung function, body composition, muscle strength, and physical performance.
Participants will undergo comprehensive phenotyping that includes spirometry, respiratory muscle strength testing, six-minute walk testing, handgrip strength, sit-to-stand testing, body composition assessment, diaphragm ultrasound, and non-contrast CT imaging of the lungs and thighs. Blood samples will be collected for biomarker, proteomic, metabolomic, genomic, and immunologic analyses. Vastus lateralis muscle biopsies will be performed at baseline and study completion to evaluate mitochondrial bioenergetics and molecular pathways associated with muscle remodeling.
Eligible participants will be adults aged 40-80 years with COPD, a smoking history of at least 10 pack-years, and overweight or obesity. Individuals with diabetes, active malignancy, recent COPD exacerbations, contraindications to tirzepatide, or conditions that could interfere with study participation will be excluded.
This pilot study is designed to generate critical mechanistic and clinical data regarding the role of GLP-1 receptor agonists in COPD. Findings will help define the relationships among obesity, adipokine signaling, systemic inflammation, skeletal muscle dysfunction, and lung disease progression, while providing preliminary efficacy estimates to support the design of a future multicenter randomized clinical trial evaluating GLP-1 therapy as a novel treatment strategy for COPD.
Detailed description
Chronic obstructive pulmonary disease (COPD) is a leading cause of morbidity and mortality worldwide and is increasingly recognized as a systemic disease that affects far more than the lungs. In addition to airflow limitation, many individuals with COPD experience chronic inflammation, loss of skeletal muscle function, reduced exercise capacity, and metabolic abnormalities that contribute substantially to disability, hospitalizations, and reduced quality of life. Obesity, which is highly prevalent among patients with COPD, further worsens these systemic manifestations through complex interactions involving inflammation, altered hormone signaling, and impaired energy metabolism. Despite the significant burden imposed by these metabolic and musculoskeletal complications, few therapies specifically target the underlying biological pathways that connect obesity, inflammation, muscle dysfunction, and lung disease.
The GLIMR COPD study is a randomized, controlled pilot clinical trial designed to investigate whether treatment with the GLP-1/GIP receptor agonist tirzepatide can improve lung function, skeletal muscle health, physical performance, and systemic inflammation in overweight and obese individuals with COPD. Beyond its established effects on weight reduction and glucose regulation, tirzepatide has demonstrated potent anti-inflammatory and metabolic benefits that may favorably influence multiple biological pathways involved in COPD progression. Emerging evidence suggests that GLP-1-based therapies can reduce inflammatory signaling, improve mitochondrial function, enhance skeletal muscle metabolism, and alter adipokine profiles, including reductions in circulating leptin, a hormone that has been strongly associated with worse COPD outcomes.
The study will enroll 30 participants with COPD, including 20 individuals receiving tirzepatide and 10 age- and sex-matched control participants. Participants will undergo detailed evaluations at baseline, six months, and twelve months. These assessments will include pulmonary function testing, exercise capacity measurements, muscle strength testing, body composition analysis, imaging studies, blood biomarker analyses, and skeletal muscle biopsies. By combining clinical assessments with advanced molecular analyses, the study seeks to understand not only whether tirzepatide improves health outcomes, but also the biological mechanisms responsible for those improvements.
The first objective of the study is to determine how tirzepatide influences systemic inflammation and immune dysfunction in COPD. Blood samples collected throughout the study will undergo comprehensive proteomic and biomarker analyses to identify changes in inflammatory pathways and circulating mediators associated with treatment. Particular attention will be given to adipokines such as leptin and adiponectin, which may serve as important links between obesity and COPD progression.
The second objective is to investigate the effects of tirzepatide on skeletal muscle health. Skeletal muscle dysfunction is a major contributor to exercise intolerance and reduced quality of life in COPD. Muscle biopsies obtained before and after treatment will be used to evaluate mitochondrial function, fatty acid oxidation, gene expression, protein signaling, and metabolic pathways that regulate muscle performance and adaptation. These studies will provide important insights into whether tirzepatide directly improves muscle bioenergetics and cellular health.
The third objective is to quantify the effects of tirzepatide on clinically meaningful outcomes. Investigators will assess changes in lung function, respiratory muscle strength, exercise capacity, muscle strength, physical performance, and body composition. Advanced CT imaging will be used to measure changes in skeletal muscle mass, visceral fat, and other body composition characteristics. These measurements will help determine whether improvements in metabolic health translate into better physical function and pulmonary outcomes.
Participants eligible for enrollment will be adults aged 40-80 years with COPD and overweight or obesity. The study is being conducted through the Cleveland Clinic COPD Center, which follows more than 2,500 patients and has extensive experience in COPD clinical research and translational investigations.
The long-term goal of this project is to establish a scientific foundation for larger multicenter clinical trials evaluating incretin-based therapies as novel treatment strategies for COPD. By examining the interconnected relationships among obesity, inflammation, skeletal muscle dysfunction, and lung disease, this study has the potential to identify new therapeutic approaches that address both pulmonary and systemic manifestations of COPD. The findings may ultimately help improve physical function, quality of life, and long-term outcomes for millions of individuals living with COPD.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| COPD control | No intervention | –Participants with COPD and overweight or obesity who will not receive tirzepatide and will continue standard clinical care. Participants will complete the same research assessments as the intervention group, including blood collection, pulmonary function testing, physical performance testing, body composition assessments, imaging, and skeletal muscle biopsies, allowing comparison of clinical and biological changes over 12 months. |
| COPD tirzepatide treatment | Active comparator | Drug: TirzepatideParticipants with COPD and overweight or obesity will receive once-weekly subcutaneous tirzepatide for 52 weeks in addition to standard clinical care. Participants will undergo longitudinal assessments of lung function, skeletal muscle health, body composition, physical performance, and inflammatory biomarkers to evaluate the effects of tirzepatide on pulmonary and systemic manifestations of COPD. |
Who may qualify
- Ages
- 40 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- Age 40-80 years
- Diagnosis of chronic obstructive pulmonary disease (COPD) with post-bronchodilator FEV₁/FVC < 0.70
- GOLD stage 1-3 COPD (FEV₁ >30% predicted)
- Former smoker with a smoking history of at least 10 pack-years
- Body mass index (BMI) ≥27 kg/m² with at least one weight-related comorbidity (e.g., prediabetes, hypertension, dyslipidemia, obstructive sleep apnea, or cardiovascular disease) or BMI 30-40 kg/m²
Key exclusion criteria (17 listed)
- Type 2 diabetes mellitus (HbA1c > 6.5%)
- Pregnancy or breastfeeding
- Coagulopathy, defined as INR > 1.4 or platelet count <80,000/μL
- Active malignancy, including lung cancer
- Use of medications known to significantly alter muscle protein metabolism within 6 weeks of enrollment (e.g., oral corticosteroids, tamoxifen, high-dose estrogen, testosterone)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| TirzepatideTirzepatide is a once-weekly subcutaneous dual GIP/GLP-1 receptor agonist administered for 52 weeks using standard dose escalation as tolerated in addition to standard clinical care. | Drug | COPD tirzepatide treatment |
Primary outcome
Change in FEV1
Time frame: 12 months
Change in post-bronchodilator forced expiratory volume in one second (FEV₁) measured by standardized spirometry. FEV₁ will be compared between participants receiving tirzepatide and control participants.
6 secondary outcomes
Change in Hand Grip Strength
Time frame: 6 months and 12 months
Change in Six-Minute Walk Distance (6MWD)
Time frame: 6 months and 12 months
Change in Five Sit-to-Stand Performance
Time frame: 6 months and 12 months
Change in Lean Muscle Mass
Time frame: 12 months
Change in Serum Leptin Concentration
Time frame: 6 months and 12 months
Change in Skeletal Muscle Mitochondrial function
Time frame: 12 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Aug 2026.
- Background: PubMed 31020810Hong Y, Lee JH, Jeong KW, Choi CS, Jun HS. Amelioration of muscle wasting by glucagon-like peptide-1 receptor agonist in muscle atrophy. J Cachexia Sarcopenia Muscle. 2019 Aug;10(4):903-918. doi: 10.1002/jcsm.12434. Epub 2019 Apr 24.
- Background: PubMed 37647574Foer D, Strasser ZH, Cui J, Cahill KN, Boyce JA, Murphy SN, Karlson EW. Association of GLP-1 Receptor Agonists with Chronic Obstructive Pulmonary Disease Exacerbations among Patients with Type 2 Diabetes. Am J Respir Crit Care Med. 2023 Nov 15;208(10):1088-1100. doi: 10.1164/rccm.202303-0491OC.
- Individual participant dataSharing planned: No. There is no current plan to share individual participant data outside the study team. Any future data sharing will be considered in accordance with participant consent, institutional policies, and regulatory requirements.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Amy Attaway, MD principal investigator
The Cleveland Clinic
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Tirzepatide in people with COPD and Obesity & Overweight, run by The Cleveland Clinic at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 5 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Amy Attaway, MD (216-445-2807, attawaa@ccf.org), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in FEV1 (time frame: 12 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07747805, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Aug 2026.