A phase 3, 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
100
oral administration of TS-172 20\~60 mg/day
oral administration of placebo
Taisho Pharmaceutical Co., Ltd 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 8
Concentration of corrected serum calcium
Time frame: Up to Week 8
Serum Ca × P product
Time frame: Up to Week 8
Taisho Pharmaceutical Co., Ltd. Taisho Pharmaceutical Co., Ltd.
CONTACT
Taisho Director Taisho Director
CONTACT
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