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Clinical Trial Summary

The purpose of this study is to determine whether FG-4592 is safe and effective in the treatment of anemia in participants with lower risk MDS and low red blood cell transfusion burden.


Clinical Trial Description

This study includes an Open-Label Lead in, a Double-Blind component, and an Open-Label High Erythropoietin component. There is a screening period of up to 42 days followed by a treatment period of 52 weeks and a 4-week end of treatment assessment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03263091
Study type Interventional
Source FibroGen
Contact
Status Terminated
Phase Phase 3
Start date September 7, 2017
Completion date June 22, 2023