drugset / Trial / NCT06745531

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

NCT06745531

Phase 3 Completed 101 enrolled Taisho Pharmaceutical Co., Ltd.
RandomizedParallel-groupTriple-blindTreatment

Summary

A phase 3, randomized, placebo-controlled, double-blind study of TS-172 in hyperphosphatemia

Timeline

Start
2025-01-06
Primary completion
2025-10-13
Completion
2025-10-20

Drugs

EvaluationDrugModalityDoseRoute
Subject TS-172 Unknown 20 mg Oral
Subject TS-172 Unknown 60 mg Oral

Indications