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

26 de agosto de 2026 actualizado 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.

Descripción general del estudio

Estado

Aún no reclutando

Intervención / Tratamiento

Descripción detallada

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 estudio

Intervencionista

Inscripción (Estimado)

116

Fase

  • Fase 4

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

  • Nombre: Xiao Wang
  • Número de teléfono: 86-10-88396953
  • Correo electrónico: wangxiao@fuwai.com

Copia de seguridad de contactos de estudio

Ubicaciones de estudio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana, 100037
        • Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
        • Investigador principal:
          • Kefei Dou, MD
        • Contacto:
          • Xiao Wang, MD
          • Número de teléfono: 86-10-88396953
          • Correo electrónico: wangxiao@fuwai.com
        • Investigador principal:
          • Xiao Wang, MD
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Triple

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador de placebos: 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.

¿Qué mide el estudio?

Medidas de resultado primarias

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

Medidas de resultado secundarias

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

Otras medidas de resultado

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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

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

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

31 de diciembre de 2027

Finalización del estudio (Estimado)

31 de diciembre de 2027

Fechas de registro del estudio

Enviado por primera vez

14 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

14 de junio de 2026

Publicado por primera vez (Actual)

18 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

28 de agosto de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

26 de agosto de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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