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

F

Federico II University

Status

Enrolling

Conditions

Hypercholesterolaemia

Treatments

Drug: Praluent (Alirocumab)

Study type

Observational

Funder types

Other

Identifiers

NCT07375225
Prot. 28/2024

Details and patient eligibility

About

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

Enrollment

1,500 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

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.

Trial design

1,500 participants in 1 patient group

Subjects with hyperlipidaemia under Alirocumab 300 mg treatment.
Description:
Subjects with hyperlipidaemia
Treatment:
Drug: Praluent (Alirocumab)

Trial contacts and locations

1

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Central trial contact

Pasquale Perrone Filardi

Data sourced from clinicaltrials.gov

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