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Clinical Trial 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


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06186934
Study type Observational [Patient Registry]
Source Kyowa Kirin Co., Ltd.
Contact hyeokjun choi
Phone 01074713471
Email hyeokjun.choi.2j@kyowakirin.com
Status Recruiting
Phase
Start date December 21, 2023
Completion date January 30, 2026

See also
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