39
Participants
Start Date
April 30, 2012
Primary Completion Date
October 31, 2013
Study Completion Date
May 31, 2014
BI 655066 (very high i.v. dose)
Single very high i.v. dose BI 655066
Placebo, i.v.
Single i.v. administration of placebo
BI 655066 (high s.c. dose)
Single high s.c. dose BI 655066
BI 655066 (low i.v. dose)
Single low i.v. dose BI 655066
BI 655066 (high medium i.v. dose)
Single high medium i.v. dose BI 655066
BI 655066 (very low i.v. dose)
Single very low i.v. dose BI 655066
BI 655066 (low s.c. dose)
Single low s.c. dose BI 655066
BI 655066 (high i.v. dose)
Single high i.v. dose BI 655066
Placebo, s.c.
Single s.c. administration of placebo
BI 655066 (low medium i.v. dose)
Single low medium i.v. dose BI 655066
1311.1.0007 Boehringer Ingelheim Investigational Site, Burbank
1311.1.0008 Boehringer Ingelheim Investigational Site, Miami
1311.1.0003 Boehringer Ingelheim Investigational Site, Port Orange
1311.1.0005 Boehringer Ingelheim Investigational Site, Normal
1311.1.0006 Boehringer Ingelheim Investigational Site, Evansville
1311.1.0004 Boehringer Ingelheim Investigational Site, North Dartmouth
1311.1.0002 Boehringer Ingelheim Investigational Site, Pittsburgh
1311.1.4901 Boehringer Ingelheim Investigational Site, Berlin
1311.1.0009 Boehringer Ingelheim Investigational Site, Leeds
Lead Sponsor
Collaborators (1)
Boehringer Ingelheim
INDUSTRY
AbbVie
INDUSTRY