The purpose of this study is to compare two different formulations (test \& reference) of LY3471851 in healthy participants. This study will compare how much of each formulation gets into the blood stream and how long it takes the body to remove it. Information about any side effects that may occur will also be collected. Participants will remain in the study for about 12 weeks, after receiving the study drug that is LY3471851.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
41
Covance Dallas
Dallas, Texas, United States
Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY3471851
PK: Cmax of LY3471851
Time frame: Predose up to 56 days postdose
PK: Area Under the Concentration Versus Time Curve (AUC) of LY3471851
PK: AUC of LY3471851
Time frame: Predose up to 56 days postdose
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.