A Study of LY3437943 in Participants With Impaired and Normal Liver Function
← catalyst calendarSponsored by Eli Lilly and Company (industry) · LLY — their whole pipeline →.
Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Non randomized · None · Basic science
Enrollment
43actual
Sites
5
Country
United States
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2023-07-13 | actual | When the study began enrolling |
| Primary completion | 2025-03-02 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-03-02 | actual | The whole study's end, after follow-up |
| First posted | 2023-06-23 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-04-18 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Healthy
- Hepatic Insufficiency
Intervention
- Drug: LY3437943
Primary outcomes
what the primary-completion date above is the date OFPharmacokinetics (PK): Area under the concentration versus time curve from time zero to infinity (AUC0-∞) of LY3437943
measured Predose up to 30 days postdose
PK: Maximum observed concentration (Cmax) of LY3437943
measured Predose up to 30 days postdose
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