Expired Study
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Norristown, Pennsylvania 19403


Purpose:

The Objective of this study is to study the safety of FCM in patients with anemia caused by Heavy Uterine Bleeding and the Post Partum state.


Criteria:

Inclusion Criteria: - Female with iron deficiency anemia - Hg </= 11 Exclusion Criteria: - Previous participation in a FCM trial - Known Hypersensitivity to FCM - History of anemia other that anemia due to heavy uterine bleeding or the post partum state - current history of GI bleeding - Received IV Iron within the last 3 months - Anticipated need for surgery - Malignancy history - AST or ALT greater than normal - Received an investigational drug within 30 days of screening - Pregnant or sexually active females who are not willing ot use an effective form of birth control


NCT ID:

NCT00548860


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Norristown, Pennsylvania 19403
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 17, 2017

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