Condition: Hyperphosphatemia Patients on Hemodialysis · Sponsor: Taisho Pharmaceutical Co., Ltd.
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.
Taisho Pharmaceutical Co., Ltd. Taisho Pharmaceutical Co., Ltd. · 81-3-3985-1118 · shu_chiken@taisho.co.jp
Taisho Director Taisho Director
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| Taisho Pharmaceutical Co., Ltd selected site | Tokyo, Japan | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07285291