446
Participants
Start Date
March 31, 2005
Primary Completion Date
October 31, 2005
Study Completion Date
October 31, 2006
Darbepoetin Alfa
Initial dose, frequency and route of administration of study drug will be the same as that administered for darbepoetin alfa prior to enrollment. Frequency either once a week or once every two weeks, frequency may not change for duration of study. Route of administration either subcutaneous or intravenous, route of administration may not change for duration of study. Study drug provided in pre-filled syringes at the following unit doses: 10, 15, 20, 30, 40, 50, 60, 80, 100 or 150 ug.
Lead Sponsor
Amgen
INDUSTRY