An open-label, single-arm clinical study of TS-172 in hyperphosphatemia patients on peritoneal dialysis
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
oral administration of TS-172 20\~60 mg/day
Taisho Selected Site
Tokyo, Japan
RECRUITINGAchievement rate of the target serum phosphorus level
Time frame: Week 8
Change from baseline in serum concentration of phosphorus
Time frame: Up to Week 16
Concentration of corrected serum calcium
Time frame: Up to Week 16
Serum Ca × P product
Time frame: Up to Week 16
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