The Objective of this study is to study the safety of FCM in patients with anemia caused by chronic kidney failure
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
513
Luitpold Pharmaceuticals
Norristown, Pennsylvania, United States
Incidence of Treatment-emergent Serious Adverse Events (SAE's)
Time frame: from Day 0 through 30 days after the last dose of study drug
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