The purpose of this study is to examine the safety and tolerability of AZD2389 in participants with hepatic impairment and participants with normal hepatic function.
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Plasma PK parameter Cmax
Timeframe: pre-dose to 48 hours post-dose
Plasma PK parameter AUCinf
Timeframe: pre-dose to 48 hours post-dose
Plasma PK parameter AUClast
Timeframe: pre-dose to 48 hours post-dose