To evaluate the efficacy of KHK7791 by comparing changes in serum phosphorus levels from baseline values between hemodialysis patients with hyperphosphatemia receiving repeated administration of KHK7791 for 8 weeks and those receiving placebo.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
165
Kikuchi medical clinic
Tsukuba, Ibaraki, Japan
Changes in serum phosphorous levels from baseline values at 8 weeks after the start of administration.
Time frame: Week 8
Changes in serum phosphorous levels from baseline values at each time point.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Achievement/failure of the target serum phosphorus level (serum phosphorus level: ≤ 6.0).
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Time when the target serum phosphorus level (serum phosphorus level: ≤ 6.0) was achieved.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Achievement/failure of the target serum phosphorus level (serum phosphorus level: ≤ 5.5).
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Time when the target serum phosphorus level (serum phosphorus level: ≤ 5.5) was achieved.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Concentrations of such as Ca × P product levels at each time point.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
Changes of such as Ca × P product levels from baseline values at each time point.
Time frame: Dose period, Week 1, 2, 3, 4, 5, 6, 7, 8.
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