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Study identifier: NCT07285291 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Phase 3 Study of TS-172 in Hyperphosphatemia Patients on Hemodialysis With Phosphate Binders

Condition: Hyperphosphatemia Patients on Hemodialysis  ·  Sponsor: Taisho Pharmaceutical Co., Ltd.

PhasePhase 3
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

A phase 3, randomized, placebo-controlled, double-blind, phosphate binder-combination study of TS-172 in hyperphosphatemia patients on hemodialysis

This description comes directly from the study's public registry record.

Talk to the study team

Taisho Pharmaceutical Co., Ltd. Taisho Pharmaceutical Co., Ltd.  ·  81-3-3985-1118  ·  shu_chiken@taisho.co.jp

Taisho Director Taisho Director

Always discuss trial participation with your own doctor first.

Locations (1)

Taisho Pharmaceutical Co., Ltd selected siteTokyo, JapanRecruiting

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Source record: clinicaltrials.gov/study/NCT07285291