Overview
A Study of LY3314814 in Participants With Liver Impairment
Status:
Withdrawn
Withdrawn
Trial end date:
2018-12-01
2018-12-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of the study is to determine whether LY3314814 can be safely prescribed in participants with liver impairment without a dose adjustment. Participants will be on study for 11 days with follow-up about 7 days afterward.Phase:
Phase 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Eli Lilly and CompanyCollaborator:
AstraZeneca
Criteria
Inclusion Criteria:- Have a Body Mass Index (BMI) of 18 to 40 kilogram per meter square (kg/m²), inclusive, at
the time of screening
Exclusion Criteria:
- Have a history of or current significant ophthalmic disease, particularly any eye
problem involving the retina
- Have moderate or severe vitiligo or any other clinically significant disorder of skin
or hair pigmentation
- Have acute unstable neuropsychiatric disease
- Have active or uncontrolled neurologic disease, or clinically significant head injury