55
Participants
Start Date
October 31, 2007
Primary Completion Date
December 31, 2008
Study Completion Date
April 30, 2009
BAY60-4552
Single dose escalation planned at dose of 1 mg, 2.5 mg, 5 mg, 7.5 mg, and 10 mg
Giessen
Bad Nauheim
Lead Sponsor
Bayer
INDUSTRY