The main purpose of this study is to measure how much LY4064809 gets into the bloodstream and how long it takes the body to eliminate it in healthy participants. It also looks at safety and tolerability in healthy participants. The study drug will be administered orally. The study will last approximately 21 days, excluding screening.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
10
administered orally
Lilly Centre for Clinical Pharmacology
Singapore, Singapore
Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY4064809
PK: Cmax of LY4064809
Time frame: Predose on Day 1 Through Day 14
PK: Area Under the Concentration Versus Time Curve (AUC) of LY4064809
PK: AUC of LY4064809
Time frame: Predose on Day 1 Through Day 14
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