180
Participants
Start Date
September 30, 2006
Primary Completion Date
October 31, 2007
Study Completion Date
October 31, 2007
DNK333
DNK333 25mg b.i.d. given orally for 4 weeks
Placebo
Matching placebo
Investigative Site, Buffalo
Investigative Site, Elkin
Investigative Site, Gainesville
Investigative Site, Hollywood
Investigative Site, Miami
Investigative Site, Boca Raton
Investigative Site, Tampa
Investigative Site, Chattanooga
Investigative Site, Cincinnati
Investigative Site, Arlington Heights
Investigative Site, Rockford
Investigative Site, North Little Rock
Investigative Site, Oklahoma City
Investigative Site, Lake Jackson
Investigative Site, Colorado Springs
Investigative Site, Salt Lake City
Investigative Site, Tucson
Investigative Site, San Diego
Investigative Site, Riverside
Investigative Site, Orange
Investigative Site, Sacramento
Investigative Site, Portland
Investigative Site, Bellevue
Investigative Site, Seattle
Investigative Site, Everett
Investigative Site, Monroe
Investigative Site, Jacksonville
Investigative Site, Los Angeles
Investigative Site, Bristol
Investigative Site, Hartford
Investigative Site, New Smyrna Beach
Investigative Site, Boston
Investigative Site, Wellesley Hills
Investigative Site, Mexico
Investigative Site, Great Neck
Investigative Site, San Antonio
Investigative Site, Chesapeake
Investigative Site, Calgary
Investigative Site, St. John's
Investigative Site, Hamilton
Investigative Site, Montreal
Investigative Site, Québec
Investigative Site, Sherbrooke
Lead Sponsor
Novartis
INDUSTRY