- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07614958
Phase 3 Clinical Study Evaluating Efficacy, Safety, and Tolerability of Obicetrapib Vs Bempedoic Acid to Treat Dyslipidemia in Adults With Primary Non-familial Hypercholesterolemia or Mixed Dyslipidemia at High to Very High Cardiovascular Risk, During a Treatment Period of Approximately 84 Days (MEDICI)
A Double-Blind, Randomized, Comparative Study of Obicetrapib and Bempedoic Acid on Top of Maximally Tolerated Lipid-Lowering Therapy in Patients With Dyslipidemia at High to Very High Cardiovascular Risk
This Phase 3, randomized, double-blind, active-controlled study evaluates the efficacy and safety of obicetrapib (OBI) compared to bempedoic acid (BPA) in participants with dyslipidemia at high or very high cardiovascular risk. Participants must have elevated low density lipoprotein cholesterol (LDL-C) levels despite receiving maximally tolerated lipid lowering therapy.
The primary objective is to compare the LDL-C lowering effect of OBI (a CETP inhibitor) against BPA at 12 weeks
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Phase 3
Contacts et emplacements
Coordonnées de l'étude
- Nom: Andrea Conte, Medical Doctor
- Numéro de téléphone: +352 26497650
- E-mail: aconte@menarini.lu
Lieux d'étude
-
-
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Stockton-on-Tees, Royaume-Uni, TS19
- Recrutement
- FutureMeds North Tees
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Are male or female and ≥18 years of age at Screening (Visit 1);
Females may be enrolled if all 3 of the following criteria are met:
- Are not pregnant;
- Are not breastfeeding; and
- Do not plan to become pregnant during the study.
- Have primary non-familial hypercholesterolemia or mixed dyslipidemia and are at high to very high CV risk;
- Are on stable maximally tolerated lipid-modifying therapy for at least 8 weeks prior to Screening (Visit 1) as an adjunct to a lipid-lowering diet and lifestyle modifications, defined as a maximum tolerated statin dose, with or without ezetimibe and/or a monoclonal PCSK9-targeted therapy for at least 4 stable doses prior to Screening (Visit 1);
- Have a fasting serum LDL-C at Screening (Visit 1) of ≥70 mg/dL (1.81 mmol/L) and <130 mg/dL (3.37 mmol/L);
- Have fasting TGs <500 mg/dL (<5.7 mmol/L) at Screening (Visit 1); and
- Have an eGFR ≥30 mL/min/1.73 m2 calculated using the Chronic Kidney Disease Epidemiology Collaboration equation at Screening (Visit 1).
Exclusion Criteria:
- Have current or any previous history of New York Heart Association class III or IV HF or left ventricular ejection fraction <30%;
- Have been hospitalized for HF, with HF as the primary cause of the hospitalization, within 5 years prior to Screening (Visit 1);
- Have had any of the following clinical events within 3 months prior to Screening (Visit 1): MI; Stroke; Non-elective coronary revascularization; and/or Hospitalization for unstable angina and/or chest pain.
- Have uncontrolled severe hypertension;
- Have a formal diagnosis of definite familial hypercholesterolemia (either homozygous or heterozygous) either through genetic testing on Dutch Lipid Network criteria, Simon Broome, or MedPed;
- Have active liver disease;
- Have HbA1c ≥8.0% (≥0.080 hemoglobin fraction) or a fasting glucose ≥270 mg/dL (≥15.0 mmol/L) at Screening (Visit 1);
- Have a history of a malignancy that required surgery (excluding local and wide local excision), radiation therapy, and/or systemic therapy during the 3 years prior to Screening (Visit 1);
- Have history of full statin intolerance;
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Double
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Obicetrapib
|
Orally, Once Daily
|
|
Comparateur actif: Bempedoic Acid
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Orally, Once Daily
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
The primary efficacy endpoint is the percentage change from baseline to Day 84 in LDL-C in the OBI group compared to the BPA group.
Délai: 84 days
|
84 days
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
Percentage change from baseline to Day 84 in non-HDL-C in the OBI group compared to the BPA group
Délai: 84 days
|
84 days
|
|
Percentage change from baseline to Day 84 in HDL-C in the OBI group compared to the BPA group;
Délai: 84 days
|
84 days
|
|
Percentage change from baseline to Day 84 in ApoA1 in the OBI group compared to the BPA group;
Délai: 84 days
|
84 days
|
|
Percentage change from baseline to Day 84 in Lp(a) in the OBI group compared to the BPA group;
Délai: 84 days
|
84 days
|
|
Percentage change from baseline to Day 84 in ApoB in the OBI group compared to the BPA group;
Délai: 84 days
|
84 days
|
|
Percentage change from baseline to Day 84 in TGs in the OBI group compared to the BPA group.
Délai: 84 days
|
84 days
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- AMIL/25/Obi-Dys/001
- 2025-524265-24-00 (Ctis)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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