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A Study of Lanabecestat in Participants With Severe Kidney Impairment Compared to Healthy Participants

Renal Insufficiency Clinical Trial

Official title:
Pharmacokinetics of Lanabecestat (LY3314814) in Subjects With Impaired Renal Function

Clinical Trial Summary

The purpose of the study is to determine whether lanabecestat can be safely prescribed in participants with kidney impairment without a dose adjustment.

Participants will be on study for up to 6 weeks; this includes a 2-week screening and a follow-up about 10 days after final drug administration.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03545087
Study type Interventional
Source Eli Lilly and Company
Contact
Status Withdrawn
Phase Phase 1
Start date June 2018
Completion date January 2019
View Details
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