drugset / Trial / NCT01503736

A Randomized, Double-Blind, Placebo-Controlled Phase 3 Study of the Effects of Ferric Citrate in Subjects With End Stage Renal Disease

NCT01503736

Phase 3 Completed 183 enrolled Panion & BF Biotech Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to determine the effect and optimum dose and evaluate the safety of ferric citrate, administered three times daily (TID) immediately after meals for a total daily dose of 4 or 6 grams for 56 days, on serum phosphate (PO4) levels in subjects with end stage renal disease (ESRD).

Timeline

Start
2010-06
Primary completion
2012-06
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Ferric Citrate Unknown 4 g Oral
Subject Ferric Citrate Unknown 6 g Oral