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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

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