A phase 2, randomized, placebo-controlled, double-blind, phosphate binder-combination study of TS-172 in hyperphosphatemia patients on hemodialysis
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
62
Taisho Pharmaceutical Co., Ltd selected site
Tokyo, Japan
Achievement rate of the target serum phosphorus level
Time frame: Week 8
Change from baseline in serum concentration of phosphorus
Time frame: Up to Week 8
Concentration of corrected serum calcium
Time frame: Up to Week 8
Serum Ca × P product
Time frame: Up to Week 8
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