This study is currently not recruiting participants.

An open-label pharmacokinetic and tolerability study of eliglustat tartrate given as a single dose in subjects with mild and moderate hepatic impairment and in matched subjects with normal hepatic function STUDY NUMBER: POP13777

  • STATUS
    Not Recruiting
Updated on 19 February 2024

Summary

The purpose of this study is to investigate the pharmacokinetics of eliglustat in subjects with mild and moderate hepatic impairment, and to compare it to matched subjects with normal hepatic function to satisfy regulatory requirements.

Description

The purpose of this study is to investigate the pharmacokinetics of eliglustat in subjects with mild and moderate hepatic impairment, and to compare it to matched subjects with normal hepatic function to satisfy regulatory requirements.

Details
Condition Hepatic impairment
Age 100years or below
Clinical Study IdentifierTX5452
Last Modified on19 February 2024

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