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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
2026-05-08
Completion Date
2026-11-30
Last Updated
2026-05-15
Healthy Volunteers
No
Interventions
DRUG
TS-172 20~60 mg/day
oral administration of TS-172 20\~60 mg/day
Locations (1)
Taisho selected site
Tokyo, Japan