U.S., Dec. 17 -- ClinicalTrials.gov registry received information related to the study (NCT07285291) titled 'A Phase 3 Study of TS-172 in Hyperphosphatemia Patients on Hemodialysis With Phosphate Binders' on Dec. 03.
Brief Summary: A phase 3, randomized, placebo-controlled, double-blind, phosphate binder-combination study of TS-172 in hyperphosphatemia patients on hemodialysis
Study Start Date: Jan. 05, 2026
Study Type: INTERVENTIONAL
Condition:
Hyperphosphatemia Patients on Hemodialysis
Intervention:
DRUG: TS-172 20~60 mg/day
oral administration of TS-172 20~60 mg/day
DRUG: Placebo
oral administration of placebo
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Taisho Pharmaceutical Co., Ltd.
Disclaimer: Curated by HT Syndicatio...