Condition: Primary Hypercholesterolemia or Mixed Dyslipidemia · Sponsor: Novartis Pharmaceuticals
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).
This description comes directly from the study's public registry record.
Novartis Pharmaceuticals · +41613241111 · novartis.email@novartis.com
Novartis Pharmaceuticals
Always discuss trial participation with your own doctor first.
| Novartis Investigative Site | Yangsan, Gyeongsangnam-do, South Korea | Recruiting |
| Novartis Investigative Site | Busan, South Korea | Recruiting |
| Novartis Investigative Site | Seoul, South Korea | Recruiting |
| Novartis Investigative Site | Taegu, South Korea | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06770543