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- Essai clinique NCT07908875
Upfront Lipid-Lowering Therapy With Statins Combined With Hybutimibe in Patients With Acute Ischemic Stroke or Transient Ischemic Attack.
This study aims to evaluate whether an upfront combination lipid-lowering therapy (statins combined with hybutimibe) can further improve the 8-week LDL-C target achievement rate (<1.8 mmol/L and ≥50% reduction from baseline) compared with a sequential lipid-lowering therapy in patients with acute ischemic stroke or transient ischemic attack (TIA)
Aperçu de l'étude
Statut
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Phase 3
Contacts et emplacements
Coordonnées de l'étude
- Nom: Zhiyuan Feng
- Numéro de téléphone: 86-010-59975672
- E-mail: fzyhhz1996@gmail.com
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Definite diagnosis of acute ischemic stroke or TIA.
- Age ≥18 and <75 years
- Time from onset (last known normal) to enrollment ≤ 72 hours.
- LDL-C level ≥ 1.8 mmol/L prior to enrollment (must obtain LDL-C value after onset to be randomized).
Exclusion Criteria:
-
Use of high-intensity statins, cholesterol absorption inhibitors, PCSK9 inhibitors, or other small interfering RNA cholesterol-lowering drugs within 14 days prior to randomization.
-
Suspected familial hypercholesterolemia.
-
Suspected cardiogenic stroke (e.g., with atrial fibrillation, prosthetic heart valves, atrial myxoma, endocarditis).
-
Acute ischemic stroke suspected to be caused by other etiologies (e.g., arterial dissection, vasculitis, vascular malformation).
-
Presence of isolated sensory symptoms (e.g., numbness) only, isolated visual changes only, or isolated dizziness/vertigo only, in the absence of evidence of acute infarction on baseline head CT or MRI.
-
Pre-stroke mRS score >2.
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High risk of cerebral hemorrhage (e.g., imaging indicates hemorrhagic transformation after the current stroke, or history of hemorrhagic stroke).
-
Patients with risks or contraindications to statins or hybutimibe:
- Acute liver failure or decompensated cirrhosis.
- Known hypersensitivity to statins or hybutimibe.
- Pregnant or breastfeeding women, or women of childbearing potential who are not using effective contraceptive measures and have no documented pregnancy test.
- Use of immunosuppressants, azole antifungals, amiodarone, fibrates, or other medications that may affect statin metabolism within 14 days prior to randomization, or planned use of such medications during the study period.
- Hepatic or renal impairment (hepatic impairment defined as ALT >2× upper limit of normal [ULN] or AST >2× ULN; renal impairment defined as serum creatinine >1.5× ULN or estimated glomerular filtration rate [eGFR] <20 mL/min).
- Creatine kinase >5× ULN, or a personal or family history of hereditary muscle disease.
-
Planned major surgery or interventional procedure within 8 weeks that may require interruption of the study drug.
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Severe organic disease with a life expectancy < 8 weeks.
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Currently participating in other investigational drug or device studies.
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Inability to complete the 8-week follow-up due to geographic or other reasons (e.g., dementia, severe paralysis, psychiatric disorders).
Plan d'étude
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: Upfront combination Lipid Lowering Therapy
Patients will receive a combination of Atorvastatin (40 mg/day) and Hybutimibe (10 mg/day) immediately after enrollment, continuing for 8 weeks |
40 mg/day, administered orally 10 mg/day, administered orally. Used upfront in the experimental group, and sequentially added in the active comparator group if the 4-week LDL-C target is not met. |
|
Comparateur actif: Sequential Lipid Lowering Therapy
Patients will receive Atorvastatin (40 mg/day) immediately after enrollment for 4 weeks. An LDL-C test will be performed at 4 weeks; if the target is achieved (<1.8 mmol/L and ≥50% reduction from baseline), the same regimen will continue until 8 weeks. If the target is not achieved, Hybutimibe (10 mg/day) will be added to the regimen until 8 weeks |
40 mg/day, administered orally 10 mg/day, administered orally. Used upfront in the experimental group, and sequentially added in the active comparator group if the 4-week LDL-C target is not met. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Percentage of patients achieving the LDL-C target at 8 weeks
Délai: at 8 weeks
|
Defined as achieving an LDL-C level of <1.8 mmol/L and a reduction of ≥50% from baseline |
at 8 weeks
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Percentage change in the lipid profile at 8 weeks
Délai: at 8 weeks
|
Evaluated by the least squares mean percentage change from baseline in LDL-C, non-HDL-C, TG, TC, Lp(a), and ApoB. |
at 8 weeks
|
|
Percentage of patients achieving the general LDL-C target at 8 weeks
Délai: at 8 weeks
|
Defined as achieving an LDL-C level of <1.8 mmol/L at 8 weeks |
at 8 weeks
|
|
Incidence of composite vascular events at 8 weeks
Délai: at 8 weeks
|
Including stroke (ischemic or hemorrhagic stroke), myocardial infarction, and cardiovascular death. |
at 8 weeks
|
|
All-cause mortality rate at 8 weeks
Délai: at 8 weeks
|
Incidence of death from any cause during the study period |
at 8 weeks
|
|
Stroke recurrence rate at 8 weeks
Délai: at 8 weeks
|
Incidence of recurrent stroke events during the follow-up period |
at 8 weeks
|
|
Percentage of patients with a favorable functional outcome at 8 weeks
Délai: at 8 weeks
|
Defined as a modified Rankin Scale (mRS) score of 0 to 2 |
at 8 weeks
|
|
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 up to 8 weeks
Délai: Up to 8 weeks
|
Defined as the occurrence of any of the following prespecified safety events: study drug discontinuation or dose reduction due to intolerance, newly diagnosed diabetes, muscle-related adverse events (myalgia, myopathy, muscle necrosis), elevated liver enzymes (ALT or AST > 3 times the upper limit of normal), or major bleeding events. |
Up to 8 weeks
|
Collaborateurs et enquêteurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
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
- Troubles cérébrovasculaires
- Maladies du cerveau
- Maladies du système nerveux central
- Maladies du système nerveux
- Maladies vasculaires
- Maladies cardiovasculaires
- Ischémie cérébrale
- Accident vasculaire cérébral
- AVC ischémique
- Attaque ischémique, transitoire
- Composés hétérocycliques, 1 anneau
- Composés hétérocycliques
- Acides gras
- Lipides
- Azoles
- Pyrroles
- Acides heptanoïques
- Atorvastatine
Autres numéros d'identification d'étude
- 20260528-Hybutimibe
Plan pour les données individuelles des participants (IPD)
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Informations sur les médicaments et les dispositifs, documents d'étude
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