688
Participants
Start Date
June 30, 2008
Primary Completion Date
April 30, 2009
Study Completion Date
April 30, 2009
Aliskiren/hydrochlorothiazide (HCTZ) (300/25 mg)
During the titration period, patients received aliskiren/hydrochlorothiazide (HCTZ) 150/12.5 mg for 1 week.
Aliskiren (300 mg)
During the titration period, patients received aliskiren 150 mg for one week. Subsequently, patients were up-titrated and received aliskiren 300 mg.
Investigative Site, East Hanover
Investigative Site, Buenos Aires
Investigative Site, Quito
Investigative Site, Berlin
Investigative Site, Guatemala City
Investigative Site, Rome
Investigative Site, Basel
Investigative Site, Ankara
Lead Sponsor
Novartis
INDUSTRY