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Clinical Trial Summary

This study is to evaluate the safety and the dose-response of ASP1517 in the treatment of anemia in non-dialysis Chronic Kidney Disease (CKD) patients when ASP1517 is applied intermittently.


Clinical Trial Description

To evaluate the safety and the dose-response of ASP1517 on Hemoglobin (Hb) correction in the treatment of anemia in non-dialysis Chronic Kidney Disease (CKD) patients when ASP1517 is applied intermittently. Patients will receive ASP1517 three times a week (TIW) for first 6weeks. Patients may have the second-randomization to TIW dosing or once-a-week (QW) dosing at Week 6, 8, 10, 12, 14 or 16 if patients meet the criteria. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01964196
Study type Interventional
Source Astellas Pharma Inc
Contact
Status Completed
Phase Phase 2
Start date September 17, 2013
Completion date December 1, 2015

See also
  Status Clinical Trial Phase
Completed NCT01652872 - Strategies Using Darbepoetin Alfa to Avoid Transfusions in Chronic Kidney Disease Phase 3