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Clinical Trial Summary

The purpose of this study is to evaluate the dose response (efficacy), pharmacodynamic response, pharmacokinetics, safety, and tolerability of orally administered AKB-6548 in pre-dialysis participants with anemia with repeat dosing for 42 days.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01381094
Study type Interventional
Source Akebia Therapeutics
Contact
Status Completed
Phase Phase 2
Start date June 15, 2011
Completion date February 16, 2012

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