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.
Age range
18 Years – 45 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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