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NOT YET RECRUITING
NCT07548840
PHASE3

A Clinical Study of TS-172 in Hyperphosphatemia Patients on Hemodialysis

Sponsor: Taisho Pharmaceutical Co., Ltd.

View on ClinicalTrials.gov

Summary

An open-label, single-arm clinical study of TS-172 in hyperphosphatemia patients on hemodialysis

Official title: An Open-label, Single-arm Clinical Study of TS-172 in Hyperphosphatemia Patients on Hemodialysis

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-04

Completion Date

2026-11-30

Last Updated

2026-04-23

Healthy Volunteers

No

Interventions

DRUG

TS-172 20~60 mg/day

oral administration of TS-172 20\~60 mg/day