A Study of Pharmacokinetics and Safety of LY3537031 in Participants With Normal Renal Function and Participants With Renal Impairment
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Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Non randomized · None · Basic science
Enrollment
31actual
Sites
4
Countries
New Zealand, 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 | 2025-09-18 | actual | When the study began enrolling |
| Primary completion | 2026-04-16 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2026-04-16 | actual | The whole study's end, after follow-up |
| First posted | 2025-09-10 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-04-24 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Conditions
- Renal Impairment
- Healthy
- Renal Insufficiency
- End Stage Renal Disease (ESRD)
Intervention
- Drug: LY3537031
Primary outcomes
what the primary-completion date above is the date OFPharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of LY3537031
measured Predose on day 1 up to week 8 post dose
PK: Maximum Concentration (Cmax) of LY3537031
measured Predose on day 1 up to week 8 post dose
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