Evaluation of Efficacy and Safety of Ferric Carboxymaltose (FCM) in Patients With Iron Deficiency Anemia and Impaired Renal Function



Status:Completed
Conditions:Iron Deficiency Anemia, Renal Impairment / Chronic Kidney Disease, Anemia, Anemia
Therapuetic Areas:Hematology, Nephrology / Urology
Healthy:No
Age Range:18 - Any
Updated:2/22/2018
Start Date:August 2009
End Date:August 2011

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Randomized Evaluation of Efficacy and Safety of Ferric Carboxymaltose in Patients With Iron Deficiency Anemia and Impaired Renal Function

The primary objective of this study is to examine the efficacy and safety (cardiovascular) of
an investigational intravenous (IV) iron, ferric carboxymaltose (FCM), compared to IV iron
sucrose (Venofer) in subjects who have iron deficiency anemia (IDA) and impaired renal
function.


Inclusion Criteria:

- Male or female subjects > or = to 18 years of age.

- Chronically impaired renal function.

- Screening visit central laboratory hemoglobin < or = to 11.5 g/dL.

- Screening ferritin < or = to 100 ng/mL or < or = to 300 when transferrin saturation
(TSAT) is < or = to 30%.

- If on an erythropoiesis stimulating agent(ESA) a stable dose (+/- 20%) for 4 weeks
prior to randomization.

Exclusion Criteria:

- Known hypersensitivity reaction to any component of ferric carboxymaltose (FCM) or
Venofer.

- Previously randomized in a clinical study of Ferric Carboxymaltose (FCM).

- Requires dialysis for treatment of chronic kidney disease OR is being considered for
initiation of dialysis during the time period of this trial.

- No evidence of iron deficiency.

- Any non-viral infection.

- AST or ALT at screening as determined by central labs greater than 1.5 times the upper
limit of normal.

- Known positive hepatitis with evidence of active disease.

- Received an investigational drug within 30 days of screening.

- Alcohol or drug abuse within the past 6 months.

- Hemochromatosis or other iron storage disorders.

- Estimated life expectancy of less than 6 months, or for cancer patients, an ECOG
Performance Status greater than 1.

- Any other laboratory abnormality, medical condition or psychiatric disorder which in
the opinion of the investigator would put the subject's disease management at risk or
may result in the subject being unable to comply with study requirements.

- Pregnant or sexually-active female subjects who are not willing to use an acceptable
form of contraception.
We found this trial at
1
site
Norristown, Pennsylvania 19403
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from
Norristown, PA
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