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Clinical Trial Summary

Evaluate efficacy and safety of 16 weeks of titrated dose treatment with BAY85-3934 versus epoetin alfa/beta as measured by hemoglobin (Hb) levels. Fixed starting doses of 25, 50,75 and 150 mg of BAY85-3934 titrated at the scheduled dose control visits. Titration will be based on the subject's Hb response and tolerability of the prior dose. Planned doses include 15, 25, 50, 75, 100,150 and 200 mg/day


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01975818
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 2
Start date October 28, 2013
Completion date December 15, 2015

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