Pharmacokinetics & Preliminary Bioequivalence of Triferic (Ferric

Clinical Trial Summary

The main purpose is to determine the pharmacokinetics (PK) of Triferic iron administered via hemodialysate and via two different intravenous routes in adult patients with chronic kidney disease on chronic hemodialysis (CKD-5HD). It is an open-label, randomized single dose study.

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NCT number	NCT02739100
Study type	Interventional
Source	Rockwell Medical Technologies, Inc.
Contact
Status	Completed
Phase	Phase 1
Start date	April 2016
Completion date	July 2016

Pharmacokinetics and Preliminary Bioequivalence of Triferic (Ferric Pyrophosphate Citrate) Administered Via Hemodialysate and Intravenously to Adult CKD-5HD Patients

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms