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Clinical Trials in Italy / NCT07375225
Recruiting Observational

Evaluation of Adherence, Persistence and Efficacy of Treatment With Alirocumab 300mg in Italy

NCT07375225 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2024-12-01
Last updated
2026-01-29

Condition(s) studied

Hypercholesterolaemia

Investigational drug(s) / intervention(s)

Praluent (Alirocumab) →

Praluent (Alirocumab): Alirocumab 300 mg injection

Study summary

Evaluation of adherence, persistence and efficacy of treatment with alirocumab 300 mg in a real-life Italian population.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: \- Patients under alirocumab 300mg treatment. Exclusion Criteria: * Age \< 18 years o \> 80 years; * Patients who refuse to participate and to sign informed consent.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Federico II University of Naples, Department of Advanced Biomedical Sciences Naples Napoli Recruiting

More Federico II University trials in Italy

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07375225 on ClinicalTrials.gov ↗ ← All trials in Italy