Continuous Soluble Ferric Pyrophosphate (SFP) Iron Delivery Via Dialysate in Hemodialysis Patients

Completed · Phase 2 · Has a placebo group

Conditions studied: End Stage Renal Disease

In brief

The purpose of this study is to compare the clinical safety and efficacy of SFP in sparing the need for erythropoiesis stimulating agents (ESAs) required to maintain hemoglobin (hgb) levels in chronic hemodialysis subjects who receive SFP via the dialysate versus subjects who receive conventional dialysate without iron.

Key facts

Study ID

NCT01286012

Run by

Rockwell Medical Technologies, Inc.

People needed

108

Starts

2011-01-01

Expected to finish

2013-01-01

Last updated by the study team

2018-10-01

Who can join

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

Where it is running

• Investigator — Birmingham, Alabama, United States
• Investigator — Tempe, Arizona, United States
• Investigator — Granada Hills, California, United States
• Investigator — Colorado Springs, Colorado, United States
• Investigator — Miami, Florida, United States
• Investigator — Miami, Florida, United States
• Investigator — Albany, Georgia, United States
• Investigator — Hayden, Idaho, United States
• Investigator — Louisville, Kentucky, United States
• Investigator — New Orleans, Louisiana, United States
• Investigator — Columbus, Mississippi, United States
• Investigator — Kansas City, Missouri, United States
• Investigator — Las Vegas, Nevada, United States
• Investigator — Paterson, New Jersey, United States
• Investigator — Lexington, North Carolina, United States
• Investigator — Columbia, Tennessee, United States
• Investigator — Duncanville, Texas, United States
• Investigator — Greenville, Texas, United States
• Investigator — San Antonio, Texas, United States
• Investigator — San Antonio, Texas, United States
• Investigator — St. George, Utah, United States
• Investigator — Taylorsville, Utah, United States
• Investigator — Fajardo, Puerto Rico

Full record on ClinicalTrials.gov

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