A Clinical Study of TS-172 in Hyperphosphatemia Patients on Peritoneal Dialysis
NCT07548853 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2026-05-15
Summary
An open-label, single-arm clinical study of TS-172 in hyperphosphatemia patients on peritoneal dialysis
Conditions
- Hyperphosphatemia Patients on Peritoneal Dialysis
Interventions
- DRUG
-
'TS-172 20~60 mg/day
oral administration of TS-172 20\~60 mg/day
Sponsors & Collaborators
-
Taisho Pharmaceutical Co., Ltd.
lead INDUSTRY
Principal Investigators
-
Taisho Director · Taisho Pharmaceutical Co., Ltd.
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-04-30
- Primary Completion
- 2027-05-31
- Completion
- 2027-05-31
Countries
- Japan
Study Locations
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