313
Participants
Start Date
March 31, 2004
Primary Completion Date
August 31, 2005
Study Completion Date
August 31, 2005
Darbepoetin alfa
Darbepoetin alfa was administered IV, every week or every 2 weeks during Weeks 1 through 52.
methoxy polyethylene glycol-epoetin beta [Mircera]
RO0503821 was administered IV, every 2 weeks during Weeks 1 through 52. The starting dose of RO0503821 (60, 100, or 180 micro gram \[µg\]) was based on the dose of darbepoetin alfa at the time of randomization (\< 40, 40 to 80, or \> 80 µg per week, respectively).
Lausanne
Brussels
Brussels
Sydney
Gosford
Parkville
Clayton
Liège
Roskilde
Brisbane
Odense
Aarau
Graz
Aalborg
Aalst
Córdoba
Stockholm
Lecco
Bergamo
Pavia
Madrid
Toulouse
Oviedo
Montpellier
Hannoversch Münden
Salamanca
Santander
Livorno
Tarbes
Karlstad
Strasbourg
Villingen-Schwenningen
Nuremberg
Aubervilliers
Messina
Blacktown
Calgary
Edmonton
Kamloops
Vancouver
Winnipeg
Halifax
Kitchener
Mississauga
HUS
Nice
Badalona
Barcelona
Hoffmann-La Roche
INDUSTRY