718
Participants
Start Date
February 28, 2003
Primary Completion Date
November 30, 2003
Study Completion Date
April 30, 2004
rHuEPO
rHuEPO 40,000U QW for 4 weeks. Dose will be increased to 60,000U/week at week 5 if inadequate response through week 12.
Darbepoetin alfa
4.5 mcg/kg QW for 4 weeks then Q3W starting at week 5 through week 11.
Lead Sponsor
Amgen
INDUSTRY