A Study of Multiple Olomorasib (LY3537982) Capsules in Healthy Participants
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Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · None · Basic science
Enrollment
120actual
Sites
2
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 | 2025-07-11 | actual | When the study began enrolling |
| Primary completion | 2025-11-08 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-11-08 | actual | The whole study's end, after follow-up |
| First posted | 2025-06-29 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-05-29 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Healthy
Intervention
- Drug: Olomorasib — also filed as LY3537982
Primary outcomes
what the primary-completion date above is the date OFPharmacokinetics (PK): Area Under the Concentration versus Time Curve from Time Zero to Time t (AUC[0-tlast]) of Olomorasib
measured From Day 1, Predose up to 72 hours Postdose
PK: Area Under the Concentration versus Time Curve from Zero to Infinity (AUC[0-∞]) of Olomorasib
measured From Day 1, Predose up to 72 hours Postdose
PK: Maximum Observed Drug Concentration (Cmax) of Olomorasib
measured From Day 1, Predose up to 72 hours Postdose
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