To evaluate the effect and safety of a switch from phosphate binders to KHK7791 to treat Hyperphosphatemia in patients on HD.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
67
KHK7791 30 mg, 20 mg ,10 mg or 5 mg tablets
Study Site 1
Niigata, Japan
Percentage of subjects who reduce the total number of taking phosphate binder tablets at the last assessment from baseline.
Time frame: Week 26
Serum phosphorus levels at each time point after the start of treatment
Time frame: up to Week 26
Corrected serum calcium level at each time point after the start of treatment
Time frame: up to Week 26
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