Condition: Iron Deficiency Anemia · Sponsor: AMAG Pharmaceuticals, Inc.
This is a Phase 3, randomized, open-label, multicenter, study in male and female pediatric subjects (2 years to \<18 years of age) with IDA, or felt by their clinician to be at risk of developing IDA. This study allows for enrollment of subjects with IDA regardless of etiology, except for CKD subjects (pediatric CKD subjects are being studied in a separate ferumoxytol protocol).
This description comes directly from the study's public registry record.
Clinical Trial Interest · 1-877-374 -4177 · CTInterest@covispharma.com
Always discuss trial participation with your own doctor first.
| Arkansas Children's Hospital | Little Rock, Arkansas, United States | Not Yet Recruiting |
| University of Florida | Gainesville, Florida, United States | Not Yet Recruiting |
| Optimus U Corporation | Miami, Florida, United States | Recruiting |
| Biomedical Research LLC | Miami, Florida, United States | Recruiting |
| Gwinnett Research Institute | Buford, Georgia, United States | Not Yet Recruiting |
| Sun Research Institute | San Antonio, Texas, United States | Recruiting |
| JSC Saules seimos medicinos centras | Kaunas, Lithuania | Not Yet Recruiting |
| Klaipeda Children's Hospital | Klaipėda, Lithuania | Not Yet Recruiting |
| Children's Hospital-Affiliate of Vilnius University Hospital Santariskiu Klinikos | Vilnius, Lithuania | Not Yet Recruiting |
| Osrodek Badan Klinicznych In Vivo sp. z o.o. | Bydgoszcz, Poland | Not Yet Recruiting |
| Prywatny Gabinet Lekarski Dr N. med. Jerzy Brzostek | Dębica, Poland | Not Yet Recruiting |
| Pro Familia Altera Sp. z o.o. | Katowice, Poland | Not Yet Recruiting |
+ 3 more locations — full list on the registry record.
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT03893045