120
Participants
Start Date
October 31, 2007
Primary Completion Date
October 31, 2009
Study Completion Date
October 31, 2009
Methoxy polyethylene glycol-epoetin beta
Mircera will be administered intravenously every 4 weeks for a total of 52 weeks. The first dose of 120, 200, or 360 mcg will be determined by the dose of ESA received prior to administration of study treatment, while subsequent doses will be adjusted to maintain hemoglobin within a country-specific target range.
Lausanne
Vienna
Vienna
Vienna
Vienna
Geneva
Vienna
Sion
Sankt Pölten
Burgdorf
Linz
Basel
Steyr
Liestal
Salzburg
Lucerne
Kufstein
Bellinzona
Locarno
Feldkirch
Mendrisio
Bregenz
Lugano
Graz
Zurich
Zurich
Sankt Gallen
Hoffmann-La Roche
INDUSTRY