62
Participants
Start Date
April 1, 2012
Primary Completion Date
August 1, 2012
Study Completion Date
August 1, 2012
BI 411034
Low dose solution for oral administration
Placebo
Solution for oral administration
BI 411034
Medium dose solution for oral administration
BI 411034
Low dose solution for oral administration
BI 411034
High dose solution for oral administration
BI 411034
High dose solution for oral administration
BI 411034
Medium dose solution for oral administration
BI 411034
High dose solution for oral administration
BI 411034
Medium dose solution for oral administration
1308.1.1 Boehringer Ingelheim Investigational Site, Ingelheim
Lead Sponsor
Boehringer Ingelheim
INDUSTRY