drugset / Trial / NCT01191255

A 58-Week Safety and Efficacy Trial of Ferric Citrate in Patients With ESRD on Dialysis

NCT01191255

Phase 3 Completed 441 enrolled Keryx Biopharmaceuticals
RandomizedFactorialOpen-labelPrevention

Summary

This is up to a 58 week study comparing ferric citrate to active control for 52 weeks in ESRD dialysis patients, and subsequently comparing ferric citrate to placebo for 4 weeks.

Timeline

Start
2010-10
Primary completion
2013-01
Completion
2013-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Calcium carbonate Other / unclassified
Subject Ferric Citrate Unknown
Subject sevelamer Other / unclassified