Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

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

26 de agosto de 2026 atualizado por: 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.

Visão geral do estudo

Status

Ainda não está recrutando

Descrição detalhada

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.

Tipo de estudo

Intervencional

Inscrição (Estimado)

116

Estágio

  • Fase 4

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

    • Beijing Municipality
      • Beijing, Beijing Municipality, China, 100037
        • Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
        • Investigador principal:
          • Kefei Dou, MD
        • Contato:
        • Investigador principal:
          • Xiao Wang, MD
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Triplo

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador de Placebo: Placebo
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.
Experimental: 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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Change in total non-calcified plaque volume (NCPV) by CCTA from baseline to 52 weeks
Prazo: Baseline and 52 weeks
Baseline and 52 weeks

Medidas de resultados secundários

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

Outras medidas de resultado

Medida de resultado
Prazo
Change in liver stiffness measurement by vibration-controlled transient elastography from baseline to 52 weeks
Prazo: Baseline and 52 weeks
Baseline and 52 weeks
Change in controlled attenuation parameter by vibration-controlled transient elastography from baseline to 52 weeks
Prazo: Baseline and 52 weeks
Baseline and 52 weeks

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

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

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de setembro de 2026

Conclusão Primária (Estimado)

31 de dezembro de 2027

Conclusão do estudo (Estimado)

31 de dezembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

14 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

14 de junho de 2026

Primeira postagem (Real)

18 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

28 de agosto de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

26 de agosto de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever