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RECRUITING
NCT06186934
Post Marketing Surveillance Study to Observe Safety and Effectiveness of NEPHOXIL ® in S. Korea Patients
Sponsor: Kyowa Kirin Korea Co., Ltd.
View on ClinicalTrials.gov
Summary
The objective of this post-marketing surveillance (PMS) study is to assess the safety and effectiveness of Nephoxil capsule 500 mg (Ferric Citrate 500 mg, equivalent to 105 mg Ferric Iron) in routine clinical settings
Key Details
Gender
All
Age Range
19 Years - Any
Study Type
OBSERVATIONAL
Enrollment
600
Start Date
2023-12-21
Completion Date
2026-01-30
Last Updated
2024-04-29
Healthy Volunteers
Yes
Conditions
Interventions
DRUG
the standard-dose group (4 g/day)
Patients with chronic kidney disease undergoing hemodialysis and controlling hyperphosphatemia
Locations (1)
Jesus Hospital
Jeonju, South Korea