A clinical study to evaluate the long-term safety and efficacy of TS-172 in hyperphosphatemia patients on hemodialysis.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
300
oral administration of TS-172 20\~60 mg/day
Taisho Pharmaceutical Co., Ltd selected site
Tokyo, Japan
RECRUITINGIncidence of adverse events
Time frame: Up to 26 weeks or up to 52 weeks
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