126
Participants
Start Date
May 31, 2012
Primary Completion Date
May 31, 2013
Study Completion Date
May 31, 2013
HPP404
Administered orally once daily for 26 weeks
Placebo
Administered orally once daily for 26 weeks
Site 2, New York
Site 6, Richmond
Site 7, Norfolk
Site 5, High Point
Site 1, Charlotte
Site 11, Augusta
Site 12, Louisville
Site 3, Valparaiso
Site 10, Saint Paul
Site 9, Hyannis
Lead Sponsor
High Point Pharmaceuticals, LLC.
INDUSTRY