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Clinical Trial Summary

This observation study is to evaluate blood lipid-lowering effects and liver/renal safety, changes in HbA1c and FPG in patients with dyslipidemia who administered CREZET tablets for 24 weeks.


Clinical Trial Description

A subject who is diagnosed with dyslipidemia and scheduled to administer CREZET tablets, will be enrolled in this study based on the doctor's medical decision. The CREZET Tablet will be administered for 24 weeks, and the data including demographic information, body measurement, vital signs and etc will be collected during the study period. The data collection point is as follows. 1. Visit 1 (baseline, day 0) 2. Visit 2 (at 12 weeks) 3. Visit 3 (at 24 weeks) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05889143
Study type Observational
Source Daewoong Pharmaceutical Co. LTD.
Contact SaeKyung Hong
Phone 82-02-550-8563
Email skhong129@daewoong.co.kr
Status Recruiting
Phase
Start date May 24, 2023
Completion date June 30, 2024

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