Leqvio rPMS (Regulatory Post-Marketing Surveillance in Korea)
Recruiting
Observational Study
Primary Hypercholesterolemia or Mixed Dyslipidemia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 – 100
- Sex
- Any
- Study type
- Observational
- Participants needed
- 1,500 (estimated)
- Sponsor
- Novartis Pharmaceuticals · Industry
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About This Trial
This non-interventional study is a mandatory regular Post Marketing Surveillance(rPMS) granted by the Korean health authorities, and is conducted to assess the effectiveness and safety of Leqvio® Pre-filled Syringe(inclisiran sodium) in routine clinical practice for the approved indications (primary hypercholesterolemia or mixed dyslipidemia).
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
If a subject meets all of the following criteria, he/she can participate in this study:
1. Adult patients(18 years or older) who have hypercholesterolemia or mixed dyslipidemia and are prescribed Leqvio® Pre-filled Syringe(inclisiran sodium) according to domestically approved p…
Contacts
Novartis Pharmaceuticals
CONTACT