This is a multi-center, open-labeled, non-comparative study to examine the safety and efficacy of ASP1585 in chronic kidney disease and hyperphosphatemia patients on peritoneal dialysis.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
35
oral
Unnamed facility
Chugoku, Japan
Unnamed facility
Chūbu, Japan
Unnamed facility
Kantou, Japan
Serum phosphorus level at treatment discontinuation
Time frame: During the 12-week treatment period
Percent of the patients meeting the target range of serum phosphorus levels
Time frame: During treatment
Time-course changes in serum calcium levels
Time frame: During Treatment
Changes in serum Ca x P
Time frame: During Treatment
Changes in intact PTH levels
Time frame: During Treatment
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