Lilly Centre for Clinical Pharmacology
Singapore, 138623
NCT Number: NCT07247357
The main purpose of this study is to measure how much LY4064809 gets into the bloodstream and how long it takes the body to eliminate it in healthy participants. It also looks at safety and tolerability in healthy participants. The study drug will be administered orally. The study will last approximately 21 days, excluding screening.
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Notify Me21 year–55 year
All sexes
Interventional
Phase 1
Singapore, 138623
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
administered orally
Time frame: Predose on Day 1 Through Day 14
PK: Cmax of LY4064809
Time frame: Predose on Day 1 Through Day 14
PK: AUC of LY4064809
Eli Lilly and Company
Industry
A Phase 1, Open-Label Study of the Pharmacokinetics of LY4064809 in Healthy Adult Chinese Participants
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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