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A Study of Effects of Selpercatinib in Hepatically Impaired Participants and Healthy Participants

Healthy Clinical Trial

Official title:
Open-label, Nonrandomized, Single-dose, Parallel-group, Safety, Tolerance, and Pharmacokinetic Study of LOXO-292 Administered to Fasted Hepatically Impaired Male and Female Subjects and Fasted Matched-control Healthy Subjects

Clinical Trial Summary

The main purpose of this study is to assess how selpercatinib gets into the blood stream and how long it takes the body to remove it when administered to participants with impaired hepatic function compared to healthy participants. Information about safety and tolerability will be collected. The study will last up to about 7 weeks, inclusive of screening period.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05436912
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 1
Start date December 10, 2018
Completion date October 30, 2019
View Details
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