30
Participants
Start Date
December 31, 2008
Primary Completion Date
November 30, 2009
Study Completion Date
November 30, 2009
NP031112
unidose sachets containing dry powder for oral suspension, once daily dosing 400 mg (4 to 20 weeks), 600 mg(4 to 16 weeks),800 mg (6 to 12 weeks), 1000 mg (6 weeks)
Placebo
unidose sachets containing dry powder for oral suspension, once daily dosing 400 mg (4 to 20 weeks), 600 mg(4 to 16 weeks),800 mg (6 to 12 weeks), 1000 mg (6 weeks)
Pharmacologische Studiecentrum Chemnitz, Chemnitz
Arzneimittelforschung Leipzig GmbH, Leipzig
Studienzentrum PD Dr. Steinwachs, Nuremberg
Lead Sponsor
Noscira SA
INDUSTRY