This is a multi-center, open-labeled, non-comparative study to examine the safety and efficacy of ASP1585 for long-term dosing in chronic kidney disease patients with hyperphosphatemia not on dialysis.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
105
oral
Unnamed facility
Chūbu, Japan
Unnamed facility
Hokkaido, Japan
Unnamed facility
Kansai, Japan
Unnamed facility
Kanto, Japan
Unnamed facility
Kyushu, Japan
Time-course changes in serum phosphorus levels
Time frame: During 48 week treatment
Achievement rate of the target range of serum phosphorus level
Time frame: During 48 week treatment
Time to achieve the target range of serum phosphorus level
Time frame: During 48 week treatment
Time-course changes in serum calcium levels
Time frame: During 48 week treatment
Time-course changes in serum intact PTH (parathyroid hormone) levels
Time frame: During 48 week treatment
Safety assessed by the incidence of adverse events, vital signs, labo-tests and 12-lead ECGs
Time frame: During 48 week treatment
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