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

Outcome

Met primary endpoint

registry Placebo-EAP vs KRX-0502 (Ferric Citrate)-EAP; p <0.0001; ANCOVA NCT01191255 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Ferric Citrate Unknown — —
Subject calcium acetate Other / unclassified — —
Subject sevelamer Other / unclassified — —