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Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of Nephoxil capsule administration for the improvement of hyperphosphatemia in CKD patients undergoing hemodialysis under actual conditions of routine medical care.


Clinical Trial Description

This study is a prospective observational study, and only observable information is collected during Visits 1 to 13 of the subjects' routine outpatient visits. Therefore, no further visits related to this study are planned, and all treatments, examinations, and evaluations necessary for the subjects shall be conducted at the discretion of the investigator. The initial dose of Nephoxil capsules for the subjects participating in this study shall be determined at the investigator's discretion, and subjects shall be classified into either the low-dose group (1.5 g/day) or the standard-dose group (4 g/day) according to the initial dose. During the observation period, dose titration within 1 g may be performed at the investigator's discretion, and in such cases, the maximum dose per day shall not exceed 6 g. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06206135
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 December 31, 2025

See also
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