A Trial Comparing Ferumoxytol With Placebo for the Treatment of Iron Deficiency Anemia
Status: | Completed |
---|---|
Conditions: | Iron Deficiency Anemia, Anemia |
Therapuetic Areas: | Hematology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 6/13/2018 |
Start Date: | June 19, 2010 |
End Date: | October 22, 2012 |
A Phase III, Randomized, Double-Blind, Placebo-Controlled Trial of Ferumoxytol for the Treatment of Iron Deficiency Anemia
To evaluate the efficacy and safety of intravenous (IV) ferumoxytol compared with placebo for
the treatment of iron deficiency anemia (IDA).
the treatment of iron deficiency anemia (IDA).
Key Inclusion Criteria include:
1. Males and females ≥18 years of age
2. Participants with IDA defined as having:
1. Hemoglobin <10.0 g/deciliter (dL)
2. Transferrin saturation <20%
3. Participants who have a history of unsatisfactory oral iron therapy or in whom oral
iron cannot be used
4. Female participants of childbearing potential who are sexually active must be on an
effective method of birth control for at least 1 month prior to screening and agree to
remain on birth control until completion of participation in the study
Key Exclusion Criteria include:
1. History of allergy to IV iron
2. Allergy to two or more classes of drugs
3. Participants on dialysis or with an estimated glomerular filtration rate <30
mL/minute/1.73 m^2
4. Female participants who are pregnant, intend to become pregnant, are breastfeeding,
within 2 weeks postpartum, or have a positive serum/urine pregnancy test
5. Hemoglobin ≤7.0 g/dL
6. Serum ferritin >600 nanograms/mL
We found this trial at
109
sites
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