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- Klinische proef NCT07657676
Effect of Mazdutide on Coronary Plaque in Patients With Coronary Atherosclerosis and Overweight or Obesity
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
Studie Overzicht
Toestand
Interventie / Behandeling
Gedetailleerde beschrijving
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.
Studietype
Inschrijving (Geschat)
Fase
- Fase 4
Contacten en locaties
Studiecontact
- Naam: Xiao Wang
- Telefoonnummer: 86-10-88396953
- E-mail: wangxiao@fuwai.com
Studie Contact Back-up
- Naam: Fang Luo
- Telefoonnummer: 86-10-88396953
- E-mail: luofang@fuwaihospital.org
Studie Locaties
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Beijing Municipality
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Beijing, Beijing Municipality, China, 100037
- Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
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Hoofdonderzoeker:
- Kefei Dou, MD
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Contact:
- Xiao Wang, MD
- Telefoonnummer: 86-10-88396953
- E-mail: wangxiao@fuwai.com
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Hoofdonderzoeker:
- Xiao Wang, MD
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Contact:
- Luo Fang
- Telefoonnummer: 86-10-88396953
- E-mail: luofang@fuwaihospital.org
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Age ≥ 18 years
- 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).
- Coronary stenosis 30-70% confirmed by CAG or CCTA within 3 months prior to enrollment.
- Signed informed consent
- Willing to comply with follow-up
Exclusion Criteria:
History or evidence of the following :
- A history of severe hypoglycemia, or recurrent symptomatic hypoglycemia (≥2 episodes) within the past six months
- 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%
- A hemorrhagic/ischemic stroke or transient ischemic attack within six months prior to screening
- A history of acute or chronic pancreatitis, gallbladder/bile duct disease, or pancreatic injury
- Presence of severe diseases such as malignant tumors, lymphoma, liver cirrhosis, HIV-positive status, etc., with an expected survival of less than 2 years
- Contraindications to GLP-1/GCG dual receptor agonists, such as hypersensitivity or severe intolerance
- A personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia syndrome type 2
Use of the following medications or treatments prior to screening :
- Use of weight-affecting medications (e.g., systemic steroids, tricyclic antidepressants, psychiatric/sedative medications, etc.) within three months prior to screening
- Use of GLP-1 RA or GIP/GLP-1 RA (exposure to investigational drugs) within three months prior to screening
- Participation in other clinical trials (exposure to investigational drugs) within three months prior to screening
- Known clinically significant abnormal gastric emptying or current use of medications that directly affect gastrointestinal motility
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)
- Serum calcitonin ≥50 ng/L (pg/mL)
- ALT/AST >3.0 × ULN
- eGFR <30 mL/min/1.73m²
- Abnormal thyroid function (TSH >6 mIU/L or <0.4 mIU/L)
- Pregnancy, planned pregnancy, or breastfeeding
- 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
- 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
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verdrievoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Placebo-vergelijker: Placebo
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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.
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Experimenteel: Experimental: Mazdutide
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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.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
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Change in total non-calcified plaque volume (NCPV) by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Change in RCA pericoronary fat attenuation index (RCA-FAI) by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in LAD pericoronary fat attenuation index (LAD-FAI) by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in LCX pericoronary fat attenuation index (LCX-FAI) by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in lesion pericoronary fat attenuation index (lesion-FAI) by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in total plaque volume (TPV) by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in percent atheroma volume (PAV) by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in low-attenuation plaque volumes by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in fibrous plaque volumes by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in fibrofatty plaque volumes by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in calcified plaque volumes by CCTA from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in total cholesterol from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in triglycerides from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in LDL-C from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in non-HDL-C from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in ApoB from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in HbA1c from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Changein fasting glucose from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in uric acid from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in Lp(a) from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in hs-CRP from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in IL-6 from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in TNF-α from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in body weight from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in waist circumference from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in waist-to-hip ratio from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in SBP from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in DBP from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Incidence of major adverse cardiovascular events (MACE) at 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Andere uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
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Change in liver stiffness measurement by vibration-controlled transient elastography from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Change in controlled attenuation parameter by vibration-controlled transient elastography from baseline to 52 weeks
Tijdsspanne: Baseline and 52 weeks
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Baseline and 52 weeks
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Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: Xiao Wang, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
- Hoofdonderzoeker: Ke fei Dou, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Vaatziekten
- Hart-en vaatziekten
- Voedingsstoornissen
- Pathologische aandoeningen, anatomisch
- Hartziekten
- Overvoeding
- Lichaamsgewicht
- Myocardiale ischemie
- Pathologische aandoeningen, tekenen en symptomen
- Voedings- en stofwisselingsziekten
- Tekenen en symptomen
- Overgewicht
- Obesitas
- Hart-en vaatziekte
- Plaque, amyloïde
- Mazdutide
Andere studie-ID-nummers
- 2026-3068
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
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