75
Participants
Start Date
September 23, 2014
Primary Completion Date
July 16, 2016
Study Completion Date
July 16, 2016
Riociguat (Adempas, BAY63-2521)
Participants received therapy with riociguat during a 10-week titration phase. The starting dose for riociguat for all patients was 0.5 milligram (mg) three times a day (TID). The dose of riociguat was increased every 2 weeks in 0.5 mg increments to 1.0, 1.5, 2.0, and 2.5 mg until patients reached their individual optimal dose based on their systolic blood pressure and well-being. After reaching their optimal dose, patients then entered a maintenance phase and remained on this dose for an additional 14 weeks. End of treatment was reached at Visit 10 after 24 weeks of treatment with riociguat.
Mineola
New Hyde Park
Brooklyn
Albany
Liverpool
Syracuse
Pittsburgh
Philadelphia
Marietta
Austell
Atlanta
Augusta
Jacksonville
Orlando
Miami Beach
Miami
Weston
Celebration
Pascagoula
Louisville
Columbus
Toledo
Cleveland
Cincinnati
Cincinnati
Cincinnati
Indianapolis
Fort Wayne
Troy
Detroit
Iowa City
Milwaukee
Milwaukee
Sioux Falls
Chicago
Omaha
Lincoln
New Orleans
Temple
Houston
El Paso
Aurora
Tucson
Pomona
La Jolla
Moreno Valley
San Juan Capistrano
Santa Barbara
Sacramento
Portland
Hartford
Boston
Boston
North Dartmouth
Newark
Albuquerque
Stony Brook
Providence
Guaynabo
Lead Sponsor
Bayer
INDUSTRY