100
Participants
Start Date
March 19, 2017
Primary Completion Date
January 20, 2019
Study Completion Date
January 20, 2019
LY3471851
LY3471851 drug product is a sterile liquid for SC injection that may be diluted with sterile 0.9% sodium chloride solution for injection (USP) prior to administration.
Placebo
The placebo dosing solution is 0.9% sodium chloride for injection (USP).
PRA Health Sciences, Lenexa
Lead Sponsor
Eli Lilly and Company
INDUSTRY
Nektar Therapeutics
INDUSTRY