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GLP-1 Agonists for Lung Function Improvement and Muscle Restoration in COPD (GLIMR COPD)

2026년 7월 31일 업데이트: Amy Attaway, The Cleveland Clinic

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.

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.

연구 개요

상태

아직 모집하지 않음

개입 / 치료

상세 설명

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.

연구 유형

중재적

등록 (추정된)

30

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

  • 이름: Amy Attaway, MD
  • 전화번호: 216-445-2807
  • 이메일: attawaa@ccf.org

연구 연락처 백업

  • 이름: Lian Yang
  • 전화번호: 216-445-5441
  • 이메일: YANGL2@ccf.org

연구 장소

    • Ohio
      • Cleveland, Ohio, 미국, 44195
        • Cleveland Clinic
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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
  • 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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
간섭 없음: COPD control
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.
활성 비교기: COPD tirzepatide treatment
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.
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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Change in FEV1
기간: 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.
12 months

2차 결과 측정

결과 측정
측정값 설명
기간
Change in Hand Grip Strength
기간: 6 months and 12 months
Change in dominant hand grip strength measured using a calibrated hand dynamometer.
6 months and 12 months
Change in Six-Minute Walk Distance (6MWD)
기간: 6 months and 12 months
Change in time required to complete five chair rises as a measure of lower extremity muscle function and mobility.
6 months and 12 months
Change in Five Sit-to-Stand Performance
기간: 6 months and 12 months
Change in time required to complete five chair rises as a measure of lower extremity muscle function and mobility.
6 months and 12 months
Change in Lean Muscle Mass
기간: 12 months
Change in skeletal muscle mass quantified by CT imaging and bioimpedance analysis.
12 months
Change in Serum Leptin Concentration
기간: 6 months and 12 months
Change in circulating leptin concentration measured from fasting blood samples.
6 months and 12 months
Change in Skeletal Muscle Mitochondrial function
기간: 12 months
Change in mitochondrial respiratory capacity measured in vastus lateralis muscle biopsy specimens.
12 months

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Amy Attaway, MD, The Cleveland Clinic

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 8월 28일

기본 완료 (추정된)

2028년 8월 15일

연구 완료 (추정된)

2029년 8월 15일

연구 등록 날짜

최초 제출

2026년 7월 31일

QC 기준을 충족하는 최초 제출

2026년 7월 31일

처음 게시됨 (실제)

2026년 8월 5일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 8월 5일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 31일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

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.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

미국에서 제조되어 미국에서 수출되는 제품

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다