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A Study to Evaluate the Safety (Compared to Iron Sucrose), Efficacy and Pharmacokinetics of Ferumoxytol for the Treatment of Iron Deficiency Anemia (IDA) in Pediatric Subjects With Chronic Kidney Disease (CKD)

Recruiting · Phase 3 · NCT03619850

Conditions: Chronic Kidney Disease, Iron Deficiency Anemia

At a glance

Research payments reported, 2025
$51,937
U.S. investigators named
5
Sites paid
6
Planned or actual enrollment
129

About the trial

Sponsor
AMAG Pharmaceuticals, Inc.
Tested
Ferumoxytol (drug), Iron sucrose (drug)
Dates
Started 2018-08-13; completion 2026-08-31
Results posted
Not yet

Primary Objectives: To evaluate the safety (compared to iron sucrose) and efficacy of ferumoxytol in pediatric CKD subjects with iron deficiency anemia (IDA) or who are at risk of development of IDA Secondary Objective: To determine the single-dose pharmacokinetics (PK) and pharmacodynamics (PD) profile of ferumoxytol in pediatric subjects.

From ClinicalTrials.gov, last updated 2026-04-17. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Azurity Pharmaceuticals, Inc. reported $51,937 in research payments for this study in 2025 (25 payments).

Products named: Feraheme

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.