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Clinical Trial Summary

To evaluate the efficacy and safety of ferric citrate capsules for the treatment of hyperphosphatemia in patients with chronic kidney disease undergoing hemodialysis


Clinical Trial Description

This is a multicenter, randomized, open-label, active-controlled, parallel, phase III study which aims to assess the efficacy and safety of ferric citrate capsules for the treatment of hyperphosphatemia in patients with chronic kidney disease undergoing hemodialysis. This study is consisting of a Screening/Washout period (14 days) and a Treatment/Observation period (12 weeks). During the Treatment period, the subjects will be randomly assigned to the ferric citrate capsule group (study group) or sevelamer carbonate tablet group (control group) in the ratio of 1:1. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03984760
Study type Interventional
Source Panion & BF Biotech Inc.
Contact
Status Completed
Phase Phase 3
Start date June 19, 2019
Completion date February 20, 2021

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