RecruitingNCT07083206

A Study to Evaluate the Effectiveness and Safety of Fixed-Dose Combination of Pitavastatin/ Ezetimibe

A Multi-center, Prospective, Non-intervention, Observational Study to Evaluate the Effectiveness and Safety of Switching to Pevarozet Tablet in Patients With Hypercholesterolemia Previously Treated With Atorvastatin or Rosuvastatin Monotherapy


Sponsor

Ahn-Gook Pharmaceuticals Co.,Ltd

Enrollment

4,500 participants

Start Date

Jul 29, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

The objective of this study is to evaluate the effectiveness and safety of Pitavastatin/Ezetimibe FDC in patients with hypercholesterolemia.


Eligibility

Min Age: 19 Years

Plain Language Summary

Simplified for easier understanding

This observational study is collecting real-world data on how effective and safe a fixed-dose combination pill (pitavastatin/ezetimibe) is in patients with high cholesterol who are switching from statin-only therapy. The study will capture laboratory results from routine clinical visits to compare cholesterol levels before and after the switch. You may be eligible if you are 19 or older, have high cholesterol, have been on a stable statin (atorvastatin or rosuvastatin) for at least 3 months, and your doctor has already decided to switch you to the pitavastatin/ezetimibe combination. Participation involves your doctor collecting routine blood test results over time; no extra procedures or clinic visits beyond standard care are required. This summary was prepared using AI to help patients understand this research.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Locations(1)

Yongin Severance Hospital

Yongin-si, South Korea

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NCT07083206


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