To evaluate the effect and safety of KHK7791 to treat Hyperphosphatemia in ptatients on HD.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
207
Study Site 1
Nagoya, Japan
To investigate the clinically recommended dose by comparing changes in serum phosphorus levels from baseline values at Week 6.
Time frame: Week 6
Changes in serum Ca × P levels from baseline.
Time frame: Week 6
Changes in corrected serum calcium levels from baseline.
Time frame: Week 6
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