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Clinical Trial Summary

This study is to evaluate 24-week efficacy and 52 week immunogenicity of subcutaneous Eporon versus Epoetin Alfa (Eprex) in the treatment of anemia associated with chronic renal failure in pre-dialysis patients. A total of 214 patients will be enrolled in Turkey.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03521713
Study type Interventional
Source Dong-A ST Co., Ltd.
Contact Ayse Uslu
Phone 90 312 284 50 85
Email ayse.uslu@triogrup-cro.com
Status Recruiting
Phase Phase 3
Start date March 1, 2016
Completion date March 2021

See also
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