56
Participants
Start Date
April 30, 2012
Primary Completion Date
September 30, 2012
Study Completion Date
September 30, 2012
LY3016859 intravenous
Administered intravenously
Placebo intravenous
Administered intravenously
LY3016859 subcutaneous
Administered subcutaneously
Placebo subcutaneous
Administered subcutaneously
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., London
Eli Lilly and Company
INDUSTRY