The purpose of this study is to see how safe and well-tolerated the drug LY3549492 is and how it behaves in the body, when given in multiple doses to healthy people who are overweight or have obesity. Participation in the study will last approximately 8 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
60
Administered orally
Fortrea Clinical Research Unit
Daytona Beach, Florida, United States
RECRUITINGFortrea Clinical Research Unit
Dallas, Texas, United States
RECRUITINGFortrea Clinical Research Unit
Madison, Wisconsin, United States
COMPLETEDNumber 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 regardless of causality, will be reported in the Reported Adverse Events module
Time frame: Baseline through end of the Follow-up Period (Week 10)
Pharmacokinetics (PK): Maximum Observed Drug Concentration (Cmax) of LY3549492
PK: Cmax of LY3549492
Time frame: Predose on Day 1 through end of the Follow-up Period (Week 10)
PK: Observed Drug Trough Concentration (Ctrough) of LY3549492
PK: Ctrough of LY3549492
Time frame: Predose on Day 1 through end of the Follow-up Period (Week 10)
PK: Area Under the Concentration Versus Time Curve (AUC) of LY3549492
PK: AUC of LY3549492
Time frame: Predose on Day 1 through end of the Follow-up Period (Week 10)
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
CONTACT
Physicians interested in becoming principal investigators please contact
CONTACT
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