Ferumoxytol Versus Oral Iron in the Treatment of Anemia in Non-Dialysis Dependent Chronic Kidney Disease Patients
Public ClinicalTrials.gov record NCT00255424. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase III Study of the Safety and Efficacy of Ferumoxytol (Compared With Oral Iron) as an Iron Replacement Therapy in Chronic Kidney Disease Patients Not on Dialysis
Study identification
- NCT ID
- NCT00255424
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 3
- Lead sponsor
- AMAG Pharmaceuticals, Inc.
- Industry
- Enrollment
- 304 participants
Conditions and interventions
Conditions
Interventions
- ferumoxytol or oral iron Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Apr 30, 2004
- Primary completion
- Not listed
- Completion
- Jul 31, 2006
- Last update posted
- Jan 8, 2015
2004 – 2006
United States locations
- U.S. sites
- 19
- U.S. states
- 13
- U.S. cities
- 18
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Not listed | Encino | California | 91356 | — |
| Not listed | Riverside | California | 92501 | — |
| Not listed | Tarzana | California | 91356 | — |
| Not listed | Ocala | Florida | 34471 | — |
| Not listed | Shreveport | Louisiana | 71101 | — |
| Not listed | Shreveport | Louisiana | 71103 | — |
| Not listed | Springfield | Massachusetts | 01107 | — |
| Not listed | Detroit | Michigan | 48236 | — |
| Not listed | Flushing | New York | 11355 | — |
| Not listed | Orchard Park | New York | 14127 | — |
| Not listed | Columbus | Ohio | 43210 | — |
| Not listed | Hershey | Pennsylvania | 17033 | — |
| Not listed | Lancaster | Pennsylvania | 17604 | — |
| Not listed | Chattanooga | Tennessee | 37404 | — |
| Not listed | Knoxville | Tennessee | 37923 | — |
| Not listed | Houston | Texas | 77074 | — |
| Not listed | Fairfax | Virginia | 22030 | — |
| Not listed | Bluefield | West Virginia | 24701 | — |
| Not listed | Appleton | Wisconsin | 54911 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT00255424, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Jan 8, 2015 · Synced Jun 25, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT00255424 live on ClinicalTrials.gov.