Healthy Participants Clinical Trial
Official title:
Evaluation of the Safety and Pharmacokinetics of a Single Dose of Linzagolix in Female Subjects With Normal and Impaired Hepatic Function
The primary objective of this study is to assess the pharmacokinetics (PK) of linzagolix in subjects with varying degrees of impaired hepatic function compared to match control subjects with normal hepatic function
This is a Phase 1, non-randomized, open label, single-dose study to evaluate the effect of
varying degrees of impaired hepatic function (i.e., mild, moderate, and severe Hepatic
Impairment (HI)) on the PK, safety, and tolerability of linzagolix and its major metabolite,
KP017.
Up to 28 adult female participants will be enrolled.
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