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Effect of Mazdutide on Coronary Plaque in Patients With Coronary Atherosclerosis and Overweight or Obesity

2026년 8월 26일 업데이트: Xiao Wang, China National Center for Cardiovascular Diseases

Effect of Mazdutide on Coronary Plaque Progression in Patients With Coronary Atherosclerosis and Overweight or Obesity: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Trial

This multicenter, randomized, double-blind, placebo-controlled trial aims to evaluate the effect of mazdutide, a dual GLP-1/GCG receptor agonist, on coronary plaque progression assessed by coronary computed tomography angiography (CCTA) in patients with coronary atherosclerosis and overweight or obesity. The primary endpoint is the change in total non-calcified plaque volume (NCPV) from baseline to week 52. Secondary endpoints include changes in pericoronary adipose tissue inflammation (fat attenuation index, FAI), plaque composition, metabolic parameters, inflammatory biomarkers, and clinical outcomes. A substudy will include 18F-NaF PET/CT imaging.

연구 개요

상세 설명

Coronary atherosclerosis is the principal pathological substrate underlying most cardiovascular events and remains a leading cause of morbidity and mortality. Overweight and obesity are well-established independent risk factors that drive the development and progression of coronary atherosclerotic plaque, and thus represent critical modifiable targets for therapeutic intervention.

Prior studies have shown that GLP-1 receptor agonists (GLP-1RAs) provide hypoglycemic, weight-loss, and cardiovascular protective benefits. Mazdutide, the first approved GLP-1/GCG dual receptor agonist, combines GLP-1-mediated insulin secretion and appetite suppression with GCG-driven energy expenditure. Phase III trials have demonstrated robust glycemic and weight benefits, along with reductions in hs-CRP and liver fat. Given that dual-receptor activation yields more robust metabolic improvements than single-receptor agonism, mazdutide may possess greater potential than GLP-1 monotherapy in suppressing coronary plaque progression.

Therefore, we propose a multicenter, randomized, double-blind, placebo-controlled trial to evaluate the effect of 52 weeks of Mazdutide treatment on CCTA-assessed non-calcified plaque volume (NCPV) in patients with coronary atherosclerosis and overweight or obesity.

PET-CT substudy: A subset of eligible patients will be enrolled into a sub-study, we aim to evaluate the efficacy of Mazdutide on plaque inflammation assessed by 18F-NaF PET/CT.

연구 유형

중재적

등록 (추정된)

116

단계

  • 4단계

연락처 및 위치

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

연구 연락처

연구 연락처 백업

연구 장소

    • Beijing Municipality
      • Beijing, Beijing Municipality, 중국, 100037
        • Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
        • 수석 연구원:
          • Kefei Dou, MD
        • 연락하다:
        • 수석 연구원:
          • Xiao Wang, MD
        • 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:

  1. Age ≥ 18 years
  2. BMI ≥ 28 kg/m2 or BMI≥ 24kg/m2 with at least one of the following conditions: dyslipidemia, metabolic associated fatty liver disease, hypertension, prediabetes, type 2 diabetes mellitus, or obesity-related obstructive sleep apnea syndrome (at screening or within 6 months prior to screening).
  3. Coronary stenosis 30-70% confirmed by CAG or CCTA within 3 months prior to enrollment.
  4. Signed informed consent
  5. Willing to comply with follow-up

Exclusion Criteria:

  1. History or evidence of the following :

    1. A history of severe hypoglycemia, or recurrent symptomatic hypoglycemia (≥2 episodes) within the past six months
    2. Severe heart disease as determined by the investigator, including coronary artery disease that has undergone or is planned for coronary artery bypass grafting or percutaneous coronary intervention, valvular heart disease requiring valve repair or replacement, heart transplantation, severe heart failure (NYHA III-IV) or cardiogenic shock, or a known history of left ventricular ejection fraction ≤30%
    3. A hemorrhagic/ischemic stroke or transient ischemic attack within six months prior to screening
    4. A history of acute or chronic pancreatitis, gallbladder/bile duct disease, or pancreatic injury
    5. Presence of severe diseases such as malignant tumors, lymphoma, liver cirrhosis, HIV-positive status, etc., with an expected survival of less than 2 years
    6. Contraindications to GLP-1/GCG dual receptor agonists, such as hypersensitivity or severe intolerance
    7. A personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia syndrome type 2
  2. Use of the following medications or treatments prior to screening :

    1. Use of weight-affecting medications (e.g., systemic steroids, tricyclic antidepressants, psychiatric/sedative medications, etc.) within three months prior to screening
    2. Use of GLP-1 RA or GIP/GLP-1 RA (exposure to investigational drugs) within three months prior to screening
    3. Participation in other clinical trials (exposure to investigational drugs) within three months prior to screening
    4. Known clinically significant abnormal gastric emptying or current use of medications that directly affect gastrointestinal motility
  3. Laboratory test results meeting any of the following criteria at screening (repeat testing within one week is permitted if there is a clear reason, and the reason for retesting must be documented by the investigator)

    1. Serum calcitonin ≥50 ng/L (pg/mL)
    2. ALT/AST >3.0 × ULN
    3. eGFR <30 mL/min/1.73m²
    4. Abnormal thyroid function (TSH >6 mIU/L or <0.4 mIU/L)
  4. Pregnancy, planned pregnancy, or breastfeeding
  5. Contraindications to CCTA, including severe allergy to iodine contrast agents, presence of cardiac implantable electronic devices or other metal implants that may affect image analysis
  6. Inability to complete the study or comply with study requirements as determined by the investigator Exclusion criteria for the PET-CT substudy: All exclusion criteria of the main study, as well as contraindications to PET-CT examination

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: 삼루타

무기와 개입

참가자 그룹 / 팔
개입 / 치료
위약 비교기: 위약
Placebo administered subcutaneously once weekly, starting at 2 mg for 4 weeks, then escalated to 4 mg for 4 weeks, and then to 6 mg thereafter until week 52.
실험적: Experimental: Mazdutide
Mazdutide administered subcutaneously once weekly, starting at 2 mg for 4 weeks, then escalated to 4 mg for 4 weeks, and then to 6 mg thereafter until week 52.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Change in total non-calcified plaque volume (NCPV) by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks

2차 결과 측정

결과 측정
기간
Change in RCA pericoronary fat attenuation index (RCA-FAI) by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in LAD pericoronary fat attenuation index (LAD-FAI) by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in LCX pericoronary fat attenuation index (LCX-FAI) by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in lesion pericoronary fat attenuation index (lesion-FAI) by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in total plaque volume (TPV) by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in percent atheroma volume (PAV) by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in low-attenuation plaque volumes by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in fibrous plaque volumes by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in fibrofatty plaque volumes by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in calcified plaque volumes by CCTA from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in total cholesterol from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in triglycerides from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in LDL-C from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in non-HDL-C from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in ApoB from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in HbA1c from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Changein fasting glucose from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in uric acid from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in Lp(a) from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in hs-CRP from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in IL-6 from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in TNF-α from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in body weight from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in waist circumference from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in waist-to-hip ratio from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in SBP from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in DBP from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Incidence of major adverse cardiovascular events (MACE) at 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks

기타 결과 측정

결과 측정
기간
Change in liver stiffness measurement by vibration-controlled transient elastography from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks
Change in controlled attenuation parameter by vibration-controlled transient elastography from baseline to 52 weeks
기간: Baseline and 52 weeks
Baseline and 52 weeks

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Xiao Wang, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
  • 수석 연구원: Ke fei Dou, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College

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 9월 1일

기본 완료 (추정된)

2027년 12월 31일

연구 완료 (추정된)

2027년 12월 31일

연구 등록 날짜

최초 제출

2026년 6월 14일

QC 기준을 충족하는 최초 제출

2026년 6월 14일

처음 게시됨 (실제)

2026년 6월 18일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 8월 28일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 8월 26일

마지막으로 확인됨

2026년 8월 1일

추가 정보

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