The purpose of this study is to determine the safety of darbepoetin alfa beyond 16 weeks of treatment in subjects with anemia of cancer who are not receiving chemotherapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
371
Q4W
Q4W
Incidence of adverse events
Time frame: throughout study
Confirmed antibody formation to investigational product
Time frame: throughout study
Deaths on study
Time frame: on study
Laboratory parameters
Time frame: throughout study
Vital signs (blood pressure)
Time frame: throughout study
Change in PRO scores
Time frame: from baseline to end of treatment
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