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

26 agosto 2026 aggiornato da: 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.

Panoramica dello studio

Stato

Non ancora reclutamento

Intervento / Trattamento

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Stimato)

116

Fase

  • Fase 4

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Cina, 100037
        • Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
        • Investigatore principale:
          • Kefei Dou, MD
        • Contatto:
        • Investigatore principale:
          • Xiao Wang, MD
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Triplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore 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.
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
Change in total non-calcified plaque volume (NCPV) by CCTA from baseline to 52 weeks
Lasso di tempo: Baseline and 52 weeks
Baseline and 52 weeks

Misure di risultato secondarie

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

Altre misure di risultato

Misura del risultato
Lasso di tempo
Change in liver stiffness measurement by vibration-controlled transient elastography from baseline to 52 weeks
Lasso di tempo: Baseline and 52 weeks
Baseline and 52 weeks
Change in controlled attenuation parameter by vibration-controlled transient elastography from baseline to 52 weeks
Lasso di tempo: Baseline and 52 weeks
Baseline and 52 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

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

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 settembre 2026

Completamento primario (Stimato)

31 dicembre 2027

Completamento dello studio (Stimato)

31 dicembre 2027

Date di iscrizione allo studio

Primo inviato

14 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

14 giugno 2026

Primo Inserito (Effettivo)

18 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

28 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

26 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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