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Clinical Trial Summary

The objectives of this study are to assess the long-term efficacy and safety of different dose regimens of KRX-0502 in the treatment of iron deficiency anemia (IDA) in adult subjects with non-dialysis dependent chronic kidney disease (CKD).


Clinical Trial Description

This is a Phase 4, 48-week, randomized, open-label, multicenter clinical study comprised of 2 periods: a 24-week Dose Titration Period, followed by a 24-week Dose Maintenance Period. The study will consist of 12 scheduled clinic visits over a period of 48 weeks and additional visits as needed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03236246
Study type Interventional
Source Keryx Biopharmaceuticals
Contact
Status Completed
Phase Phase 4
Start date August 15, 2017
Completion date September 27, 2019

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