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Viernes 2 oct 2026SEC · NASDAQ biomédico

Calendario›SNY›ALIROCUMAB SAR236553

ALIROCUMAB SAR236553

Safety, Tolerability, and Effect of Alirocumab in High Cardiovascular Risk Patients With Severe Hypercholesterolemia Not Adequately Controlled With Conventional Lipid-modifying Therapies (ODYSSEY APPRISE)

Ensayo de Sanofi en Hipercolesterolemia.

Más ensayos de: Hipercolesterolemia.

Fase
Fase 3
Estado
Completado
Participantes
998
previstos
Centros
153
Fin del objetivo primario
abr 2019
fecha real

Qué significa cada fase y cada estado.

Estudio de intervención, de un solo grupo, abierto. Comenzó en jun 2015.

Qué mide

Percentage of Participants With Treatment Emergent Adverse Events (TEAEs) (From first injection of investigational medicinal product (IMP) up to 2 weeks after last dose of study drug (Week 120)) (del registro, en inglés)

Cómo lo describe el promotor

En el documentoEn inglés, del registroPrimary Objective: To provide participants with severe hypercholesterolemia at risk for subsequent cardiovascular (CV) events and not adequately controlled with currently available lipid-modifying therapy (LMT) access to alirocumab ahead of commercial availability and to document the overall safety and tolerability of alirocumab in this participant population. Secondary Objectives: To document the effect of alirocumab on low-density lipoprotein cholesterol (LDL-C) levels as well as non-high-density lipoprotein cholesterol (non-HDL-C), total cholesterol (total-C), high-density lipoprotein cholesterol (HDL-C), and triglyceride (TG) levels after 12 weeks of treatment. To document participant's acceptability of self-injection (Self Injection Assessment Questionnaire, SIAQ).

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Todos los de SNY, en su ficha.

Ficha completa en ClinicalTrials.gov (NCT02476006), actualizada en mar 2022.