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Clinical Trial Summary

This study is designed to characterize the excretion of bempedoic acid or bempedoic acid and ezetimibe into mature breast milk of healthy lactating women and assess the exposure to the breast fed infant by estimating the daily infant dosage and the relative infant dose (RID) of bempedoic acid or bempedoic acid and ezetimibe in breast milk after 6 consecutive daily doses of bempedoic acid or bempedoic acid/ezetimibe FCDP.


Clinical Trial Description

Post marketing approval commitment for the FDA ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06021951
Study type Interventional
Source Esperion Therapeutics, Inc.
Contact
Status Completed
Phase Phase 4
Start date August 4, 2023
Completion date March 22, 2024

See also
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Completed NCT01727791 - A Study Of Pregabalin (Lyrica) Drug Levels In Urine, Plasma And Breast Milk Of Healthy Lactating Women Phase 4