Safety Study of Soluble Ferric Pyrophosphate (SFP) in Dialysate in CKD Patients Receiving Chronic Hemodialysis

Completed · Phase 3 · Has a placebo group

Conditions studied: End Stage Renal Disease, Chronic Kidney Disease

In brief

The purpose of the parent study is to assess the short-term safety and tolerability of soluble ferric pyrophosphate (SFP) in dialysate administered to a large number of representative adult chronic kidney disease patients on hemodialysis (CKD-HD). The purpose of the extension study is to assess the long-term safety and tolerability of SFP.

Key facts

Study ID

NCT01503021

Run by

Rockwell Medical Technologies, Inc.

People needed

718

Starts

2011-11-01

Expected to finish

2014-01-01

Last updated by the study team

2016-10-25

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Study site — Mobile, Alabama, United States
• Study site — Northridge, California, United States
• Study site — Arvada, Colorado, United States
• Study site — Westminster, Colorado, United States
• Study site — Lauderhill, Florida, United States
• Study site — Marietta, Georgia, United States
• Study site — Chicago, Illinois, United States
• Study site — Peoria, Illinois, United States
• Study site — Columbus, Indiana, United States
• Study site — Wichita, Kansas, United States
• Study site — Baton Rouge, Louisiana, United States
• Study site — Shreveport, Louisiana, United States
• Study site — Camp Springs, Maryland, United States
• Study site — Gulfport, Mississippi, United States
• Study site — McComb, Mississippi, United States
• Study site — Tupelo, Mississippi, United States
• Study site — City of Saint Peters, Missouri, United States
• Study site — Lincoln, Nebraska, United States
• Study site — Reno, Nevada, United States
• Study site — Rocky Mount, North Carolina, United States
• Study site — Dayton, Ohio, United States
• Study site — Columbia, South Carolina, United States
• Research Across America — Houston, Texas, United States
• Study site — Houston, Texas, United States
• Study site — Irving, Texas, United States

Full record on ClinicalTrials.gov

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