Finding studies
Finding studies
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Lead
Astellas Pharma Europe B.V.
With
This was a phase 3, multicenter, randomized, open-label, active-controlled study. The study was planned to provide key efficacy and safety data for the approval of roxadustat in the treatment of anemia associated with CKD. Participants assigned to roxadustat treatment were administered roxadustat orally as a combination of tablets of different strengths. Participants assigned to darbepoetin alfa treatment were administered darbepoetin alfa subcutaneously or intravenously. The study consisted of 3 study periods: * Screening period: up to 6 weeks * Treatment period: 104 weeks * Follow-up period: 4 weeks until planned study end (end of year 2)
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
