Hepatic Impairment; Renal Impairment Clinical Trial
Official title:
A Multicenter Phase 0 Study In Healthy Subjects and Subjects With Either Hepatic Or Renal Impairment To Obtain Plasma For Assessment In Vitro Lenvatinib Protein Binding
E7080-A001-010 is a multicenter, parallel-group study in participants with mild, moderate, or severe hepatic or renal impairment and age-, gender-, and smoking status-matched healthy participants. The primary objective of the study is to obtain plasma from participants for use in in vitro protein binding studies.
E7080-A001-010 is a multicenter, parallel-group study in participants with mild, moderate, or
severe hepatic or renal impairment and age-, gender-, and smoking status-matched healthy
participants. Approximately 6 participants with each degree (mild, moderate, or severe) of
hepatic or renal impairment will be enrolled. Two cohorts of 8 healthy participants will be
enrolled. One cohort of healthy participants will be matched to the hepatic-impaired
participants, whereas the other will be matched to the renal-impaired participants.
The study has 2 phases. The Pre-study Phase consists of a Screening Period and a Baseline
Period. The Study Phase consists of a 2-day Study Period. No lenvatinib will be administered
in this study.
The end of the study will be the date of the last study visit for the last participant in the
study.
The following estimates are provided:
- From first participant in to last participant out, the study is expected to take
approximately one year to complete.
- The maximum estimated duration of the study for each participant is anticipated to be
approximately 5 weeks.
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