The main purpose of this study is to evaluate the safety and tolerability of LY3549492 in healthy participants. The blood tests will be performed to check how much LY3549492 gets into the bloodstream and how the body handles LY3549492. This study includes two parts and will last up to approximately 76 days for each participant, including screening.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
54
Covance Dallas
Dallas, Texas, United States
Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration
A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module
Time frame: Baseline through final follow-up at approximately Day 76
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of LY3549492
PK: AUC of LY3549492
Time frame: Predose up to 48 days postdose
PK: Maximum Concentration (Cmax) of LY3549492
PK: Cmax of LY3549492
Time frame: Predose up to 48 days postdose
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