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Clinical Trial Summary

This study will investigate the efficacy and safety based on the observation of the blood cholesterol change with Mevalotin® Tablet administration in Korean menopausal women aged 50 years or more who require treatment of dyslipidemia.


Clinical Trial Description

In this prospective, observational study, patient data (eg, clinical outcomes in actual clinical settings, demographic information, medical treatment-related information, Mevalotin® Tablet administration start date [Index date], and the lipid profile results at Week 24 after Mevalotin® Tablet administration start date) will be collected from medical records. No study drug will be administered in this study. Patient data will be used to determine the change in blood cholesterol with Mevalotin® Tablet administration (5 mg, 10 mg, 20 mg, 40 mg as determined by Investigator in clinical practice) in Korean menopausal women aged 50 years or more who require treatment of dyslipidemia. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05120895
Study type Observational
Source Daiichi Sankyo, Inc.
Contact Daiichi Sankyo Contact for Clinical Trial Information
Phone +81-3-6225-1111(M-F 9-5 JST)
Email [email protected]
Status Recruiting
Phase
Start date August 10, 2021
Completion date April 2023

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