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A Study of LY3437943 in Participants With Impaired and Normal Liver Function

Sponsored by Eli Lilly and Company

About this trial

Last updated 2 years ago

Study ID

18531

Status

Recruiting

Type

Interventional

Phase

Phase 1

Placebo

No

Accepting

18-75 Years
18 to 85 Years
All
All

Trial Timing

Ended a year ago

What is this trial about?

The main purpose of this study is to measure how much of LY3437943 gets into the bloodstream and how long it takes the body to eliminate it in participants with mild, moderate and severe impaired liver function compared to healthy participants with normal liver function. The safety and tolerability of LY3437943 will also be evaluated. The study may last up to 9 weeks for each participant including the screening period.

What are the participation requirements?

Yes

Inclusion Criteria

- Have a body mass index within the range 19.0 to 42.0 kilograms per meter squared (kg/m²), inclusive

- Healthy or various degrees of hepatic impairment depending on the study group

No

Exclusion Criteria

- Have or are anticipating an organ transplant within the next 6 months

- Requires needle evacuation of ascites fluid more than 2 times per month

- Have had variceal bleeding within 3 months of check-in, unless the participant has undergone a successful banding procedure; in that case, may check-in from 1 month after the banding procedure

Locations

Location

Status

Recruiting
Recruiting
Recruiting
Recruiting