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RECRUITING
NCT07285304
PHASE3

A Long-term Study of TS-172 in Hyperphosphatemia Patients on Hemodialysis

Sponsor: Taisho Pharmaceutical Co., Ltd.

View on ClinicalTrials.gov

Summary

A clinical study to evaluate the long-term safety and efficacy of TS-172 in hyperphosphatemia patients on hemodialysis.

Official title: A Phase 3 Long-term Study of TS-172 in Hyperphosphatemia Patients on Hemodialysis With Phosphate Binders

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

300

Start Date

2025-12-01

Completion Date

2027-07-31

Last Updated

2025-12-16

Healthy Volunteers

No

Interventions

DRUG

TS-172

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

Locations (1)

Taisho Pharmaceutical Co., Ltd selected site

Tokyo, Japan