Evaluation of Adherence, Persistence and Efficacy of Treatment With Alirocumab 300mg in Italy
- Sponsor
- Federico II University
- Study ID
- NCT07375225
- Status
- Recruiting
Conditions
- Hypercholesterolaemia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Praluent (Alirocumab) — DRUGAlirocumab 300 mg injection
Study Details
Evaluation of adherence, persistence and efficacy of treatment with alirocumab 300 mg in a real-life Italian population.
Key Dates
- Start date
- Dec 1, 2024
- Status verified
- Jan 2026
- Primary completion
- Dec 1, 2026
- Completion
- Dec 1, 2027
Study Design
- Enrollment
- 1,500 participants (estimated)
Arms
- Arm: Subjects with hyperlipidaemia under Alirocumab 300 mg treatment.Subjects with hyperlipidaemia
Primary Outcome Measure
Description of adherence of treatment with alirocumab 300mg in a real-life Italian population. [ Time Frame: 6-12-24-36 months ]
Central Contacts
- Pasquale Perrone Filardi+390817462224
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