The main purpose of this study is to evaluate the safety of a study drug known as LY3090106 in healthy Caucasian and Japanese participants. Side effects and tolerability will be documented. Blood samples will be taken to compare how the body handles the drug. The study will last about 12 weeks, not including screening or additional follow-up.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
30
Anaheim Clinical Trials, LLC
Anaheim, California, 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 Day 85
Maximum Observed Drug Concentration (Cmax) of LY3090106
Cmax of LY3090106
Time frame: Baseline through Day 85
Area Under the Concentration-Versus-Time Curve (AUC) of LY3090106
AUC of LY3090106
Time frame: Baseline through Day 85
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