Stopped: PMR release
This study will be conducted to evaluate the safety and tolerability of ferric citrate in pediatric participants with iron deficiency anemia (IDA) associated with non-dialysis dependent chronic kidney disease (NDD-CKD).
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Number of Participants with Serious and Non-serious Treatment-emergent Adverse Events
Timeframe: up to Week 28
Number of Participants with Clinically Significant Laboratory Abnormalities or Changes in Laboratory Results
Timeframe: up to Week 24
Number of Participants with Treatment-emergent Adverse Events Leading to the Discontinuation of Ferric Citrate
Timeframe: up to Week 28