49
Participants
Start Date
July 16, 2024
Primary Completion Date
December 31, 2024
Study Completion Date
December 31, 2024
LY4100511 (DC-853) Dose 1
Administered orally
LY4100511 (DC-853) Dose 2
Administered orally
LY4100511 (DC-853) Dose 3
Administered orally
Midazolam
Administered orally
Repaglinide
Administered orally
Digoxin
Administered orally
Rosuvastatin
Administered orally
Fortrea Clinical Research Unit, Dallas
DICE Therapeutics, Inc., a wholly owned subsidiary of Eli Lilly and Company
INDUSTRY