Cette page a été traduite automatiquement et l'exactitude de la traduction n'est pas garantie. Veuillez vous référer au version anglaise pour un texte source.

Icosapent Ethyl for High-Risk Coronary Plaques Assessed by 18F-NaF PET/CT (IPE-NaF)

A Randomized Controlled Trial Evaluating the Effect of Icosapent Ethyl on High-Risk Coronary Plaques Using 18F-Sodium Fluoride PET/CT

This randomized controlled study will evaluate whether icosapent ethyl (IPE) can improve and stabilize high-risk coronary plaques in patients receiving stable low-density lipoprotein cholesterol (LDL-C)-lowering therapy. Potential participants will have coronary plaques identified by coronary computed tomography angiography (CCTA), with 30% to 70% narrowing in at least one major coronary artery and at least one high-risk plaque feature.

After baseline imaging with fluorine-18 sodium fluoride positron emission tomography/computed tomography (18F-NaF PET/CT), eligible participants will be randomly assigned in a 1:1 ratio to receive either IPE 2 g twice daily plus standard LDL-C-lowering therapy or standard LDL-C-lowering therapy alone for 12 months. At the end of treatment, participants will undergo repeat CCTA and 18F-NaF PET/CT. Blood biomarkers and major adverse cardiovascular events will also be assessed during follow-up.

Aperçu de l'étude

Description détaillée

This study consists of three main stages. First, a screening cohort will be established using CCTA. Individuals with 30% to 70% diameter narrowing in at least one major coronary artery-the left anterior descending, left circumflex, or right coronary artery-and at least one high-risk plaque feature will be considered for further screening. High-risk plaque features assessed by experienced imaging specialists include increased pericoronary fat attenuation, low-attenuation plaque, positive remodeling, spotty calcification, and the napkin-ring sign. This screening process is intended to identify appropriate and reliably characterized candidates for the randomized study.

Eligible participants will undergo baseline 18F-NaF PET/CT imaging and then be randomly assigned in a 1:1 ratio using a centralized block randomization system. Participants in the intervention group will receive IPE 2 g twice daily for 12 months in addition to stable LDL-C-lowering therapy. Participants in the control group will continue stable LDL-C-lowering therapy without IPE. The LDL-C-lowering regimen should be stable for more than 4 weeks before randomization.

After 12 months, participants in both groups will undergo follow-up CCTA and 18F-NaF PET/CT to evaluate changes in coronary plaque characteristics and disease activity. Follow-up will also include measurements of relevant plasma biomarkers and monitoring for major adverse cardiovascular events. Imaging data will be acquired using standardized procedures and interpreted by experienced imaging specialists.

Type d'étude

Interventionnel

Inscription (Estimé)

100

Phase

  • Phase 4

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

  • Nom: Zheng Yin, Master
  • Numéro de téléphone: +8615359270767
  • E-mail: yinzheng@fuwai.com

Lieux d'étude

    • Beijing Municipality
      • Beijing, Beijing Municipality, Chine, 100037
        • Fuwai Hospital
        • Contact:
        • Chercheur principal:
          • Naqiong Wu, Doctor

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

  • Male or female participants aged 18 to 75 years.
  • Ability to understand the study and provide written informed consent before enrollment.
  • Receiving a stable lipid-lowering regimen before enrollment, with the type and dose of statin therapy remaining unchanged for at least 4 weeks.
  • Fasting triglyceride level below 5.6 mmol/L.
  • Presence of at least one of the following high-risk plaque features on coronary computed tomography angiography (CCTA):Pericoronary fat attenuation index greater than -70.1 Hounsfield units;
  • Low-attenuation plaque below 30 Hounsfield units;
  • Positive remodeling index greater than 1.1;
  • Spotty calcification;
  • or Napkin-ring sign, defined as a low-attenuation plaque core surrounded by a rim of higher attenuation.

Exclusion Criteria:

  • Current participation in another investigational drug, device, or procedure study, or receipt of an investigational drug or device within 4 weeks before enrollment.
  • Treatment with icosapent ethyl within 12 months before enrollment.
  • Known intolerance or hypersensitivity to icosapent ethyl or fish oil.
  • A previous diagnosis of homozygous familial hypercholesterolemia or hyperlipidemia requiring hemodialysis.
  • Myocardial infarction, unstable angina, percutaneous coronary intervention, coronary artery bypass grafting, or stroke within 3 months before enrollment;
  • Planned cardiac surgery, percutaneous coronary intervention, or carotid artery stenting, or planned major noncardiac surgery during the study.
  • A known contraindication or limitation to PET/CT, including exceeding scanner weight limits or having a device, carotid or aortic stent, or vascular graft that may cause imaging artifacts.
  • Autoimmune disease, vasculitis, or active inflammatory disease.
  • Serious infection within 1 month before enrollment or a current infection requiring intravenous antibiotic treatment.
  • Use within 6 weeks before enrollment or current use of medications that may significantly affect plaque inflammation, including oral, rectal, or injectable corticosteroids or immunosuppressive agents, such as cyclosporine, methotrexate, tacrolimus, azathioprine, antithymocyte globulin, sirolimus, anti-tumor necrosis factor agents such as infliximab, anti-interleukin-6 therapy such as tocilizumab, or anti-interleukin-1 therapy.
  • Use within 6 weeks before enrollment or current use of aspirin at a dose greater than 325 mg/day or nonsteroidal anti-inflammatory drugs at a dose greater than 1,000 mg/day.
  • Treatment within 12 months before enrollment with a cholesteryl ester transfer protein inhibitor, including anacetrapib, dalcetrapib, or evacetrapib, or with mipomersen or lomitapide.
  • Known clinically significant systemic disease, including hepatic, renal, hematologic, or malignant disease, or any other clinically significant comorbidity that may interfere with study participation or study assessments.
  • History of malignancy within the previous 5 years, except nonmelanoma skin cancer, cervical carcinoma in situ, ductal carcinoma in situ of the breast, or stage I prostate cancer.
  • Inability or anticipated inability to complete all protocol-required visits or procedures, or any condition that may make the participant unreliable for study participation, including alcohol or other substance abuse within the previous year or a psychiatric disorder.
  • Pregnancy or breastfeeding, or plans to become pregnant or breastfeed during study treatment or within 15 weeks after the last dose of study treatment.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Icosapent Ethyl Plus Standard LDL-C-Lowering Therapy
Participants will receive oral icosapent ethyl 2 g twice daily for 12 months in addition to their stable LDL-C-lowering therapy. CCTA and 18F-NaF PET/CT will be performed at baseline and after 12 months, together with biomarker and clinical event follow-up.
Icosapent ethyl will be administered orally at a dose of 2 g twice daily (total daily dose of 4 g) for 12 months, in addition to stable LDL-C-lowering therapy.
Autres noms:
  • IPE
  • Ethyl Eicosapentaenoate
  • Eicosapentaenoic Acid Ethyl Ester
Participants will continue an individualized, stable LDL-C-lowering regimen throughout the 12-month study period. The LDL-C-lowering regimen must have remained stable for more than 4 weeks before randomization. This background therapy will be administered in both study arms.
Comparateur actif: Standard LDL-C-Lowering Therapy Alone
Participants will continue their stable LDL-C-lowering therapy for 12 months without receiving icosapent ethyl. CCTA and 18F-NaF PET/CT will be performed at baseline and after 12 months, together with biomarker and clinical event follow-up.
Participants will continue an individualized, stable LDL-C-lowering regimen throughout the 12-month study period. The LDL-C-lowering regimen must have remained stable for more than 4 weeks before randomization. This background therapy will be administered in both study arms.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Absolute Change From Baseline in Maximum Target-to-Background Ratio of the Target Coronary Lesion
Délai: Baseline and Month 12
The target lesion is defined as the coronary lesion with the highest maximum target-to-background ratio (TBRmax) at baseline. TBRmax is calculated as the maximum standardized uptake value (SUVmax) of the target lesion divided by the mean standardized uptake value (SUVmean) of the blood-pool background measured in the right atrium, superior vena cava, or inferior vena cava. Absolute change is calculated as the Month 12 TBRmax minus the baseline TBRmax.
Baseline and Month 12

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Percentage Change From Baseline in TBRmax of the Target Coronary Lesion
Délai: Baseline and Month 12
The target lesion is the coronary lesion with the highest TBRmax at baseline. Percentage change is calculated as [(Month 12 TBRmax - baseline TBRmax) / baseline TBRmax] × 100%.
Baseline and Month 12
Change From Baseline in SUVmax of the Target Coronary Lesion
Délai: Baseline and Month 12
Change in the maximum standardized uptake value of the prespecified target coronary lesion, calculated as the Month 12 value minus the baseline value.
Baseline and Month 12
Change From Baseline in Total Volume of 18F-NaF-Positive Coronary Plaque
Délai: Baseline and Month 12
Total volume of coronary plaque demonstrating positive 18F-NaF uptake, defined as TBRmax greater than 1.25. Change is calculated as the Month 12 volume minus the baseline volume.
Baseline and Month 12
Change From Baseline in the Number of 18F-NaF-Positive Coronary Segments
Délai: Baseline and Month 12
Number of coronary artery segments with positive 18F-NaF uptake, defined as TBRmax greater than 1.25. Change is calculated as the Month 12 count minus the baseline count.
Baseline and Month 12
Change From Baseline in Pericoronary Fat Attenuation Index at the Target Plaque
Délai: Baseline and Month 12
Pericoronary fat attenuation index (FAI), measured in Hounsfield units using CCTA at the location of the target plaque. Change is calculated as the Month 12 value minus the baseline value.
Baseline and Month 12
Change From Baseline in Percent Atheroma Volume at the Target Plaque
Délai: Baseline and Month 12
Percent atheroma volume (PAV) will be measured using CCTA. Change is calculated as the Month 12 value minus the baseline value.
Baseline and Month 12
Change From Baseline in CCTA-Derived Coronary Plaque Component Volumes
Délai: Baseline and Month 12
CCTA will be used to measure changes in total plaque, noncalcified plaque, calcified plaque, and low-attenuation noncalcified plaque volumes. For each component, change is calculated as the Month 12 volume minus the baseline volume.
Baseline and Month 12

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Change in Plasma triglycerides Levels From Baseline to Month 12
Délai: Baseline and Month 12
Plasma levels of triglycerides (TG) will be measured.
Baseline and Month 12
Percentage Change From Baseline in Plasma High-Sensitivity C-Reactive Protein Level
Délai: Baseline and Month 12
Percentage change will be calculated as [(Month 12 hs-CRP - baseline hs-CRP) / baseline hs-CRP] × 100%.
Baseline and Month 12
Change in Plasma Eicosapentaenoic Acid Level From Baseline to Month 12
Délai: Baseline and Month 12
Plasma eicosapentaenoic acid (EPA) concentration will be measured and reported in its applicable concentration unit (e.g., μg/mL or % of total fatty acids, according to the laboratory assay).
Baseline and Month 12
Exploratory Incidence of Three-Point Major Adverse Cardiovascular Events
Délai: From randomization through Month 12
Number and percentage of participants experiencing a three-point major adverse cardiovascular event (3P-MACE), defined as the composite of all-cause death, nonfatal myocardial infarction, or nonfatal stroke.
From randomization through Month 12
Exploratory Incidence of Four-Point Major Adverse Cardiovascular Events
Délai: From randomization through Month 12
Number and percentage of participants experiencing a four-point major adverse cardiovascular event (4P-MACE), defined as 3P-MACE plus ischemia-driven coronary revascularization.
From randomization through Month 12

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 août 2026

Achèvement primaire (Estimé)

31 décembre 2028

Achèvement de l'étude (Estimé)

31 décembre 2029

Dates d'inscription aux études

Première soumission

29 juillet 2026

Première soumission répondant aux critères de contrôle qualité

11 août 2026

Première publication (Réel)

13 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

13 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

11 août 2026

Dernière vérification

1 juillet 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

Individual participant data will not be shared because of participant privacy and confidentiality considerations and applicable institutional ethics and data governance requirements. Deidentified aggregate study results may be reported in scientific publications and presentations.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Oui

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

S'abonner