The main purpose of this study is to evaluate the safety and tolerability of LY3541860 in healthy Japanese and non-Japanese participants. The study will also assess how fast LY3541860 gets into the blood stream and how long it takes the body to remove it. The study is open to healthy participants. The study will last up to approximately 113 days.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
94
P-One Clinic
Hachiōji, Tokyo, Japan
Number of Participants with One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration
A summary of TEAEs, SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module
Time frame: Baseline through Day 113
Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY3541860
PK: Cmax of LY3541860
Time frame: Predose on Day 1 through Day 113
PK: Area Under the Concentration Versus Time Curve (AUC) of LY3541860
PK: AUC of LY3541860
Time frame: Predose on Day 1 through Day 113
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