This study is the first administration of LG-0317 to humans. The purpose of the study is to evaluate safety/tolerability and pharmacokinetics in healthy subjects. The intention of this study is to provide confidence in the safety of the molecule to inform progression to further proof-of-concept studies.
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Number of participants experiencing Adverse Events (AEs) and Serious Adverse Events (SAEs)
Timeframe: Day 1 to day 18
Number of participants with clinically significant laboratory assessment abnormalities
Timeframe: Day 1 to day 18
Number of participants with clinically significant Vital sign abnormalities
Timeframe: Day 1 to day 18
Number of participants with clinically significant 12-lead electrocardiograms (ECGs) abnormalities
Timeframe: Day 1 to day 18
Number of participants with clinically significant physical examination abnormalities
Timeframe: Day 1 to day 18