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To evaluate the effect and safety of KHK7791 to treat Hyperphosphatemia in ptatients on HD.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| KHK7791 A | Experimental | Patients take KHK7791 low dose BID. |
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| KHK7791 B | Experimental | Patients take KHK7791 middle dose BID. |
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| KHK7791 C | Experimental | Patients take KHK7791 high dose BID. |
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| KHK7791 D | Experimental | Patients start at KHK7791 high dose and can down titrate weekly ,based on a GI tolerability question. |
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| Placebo | Placebo Comparator | Patients take Placebo BID. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| KHK7791 | Drug | oral administration |
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| Measure | Description | Time Frame |
|---|---|---|
| To investigate the clinically recommended dose by comparing changes in serum phosphorus levels from baseline values at Week 6. | Week 6 |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in serum Ca × P levels from baseline. | Week 6 | |
| Changes in corrected serum calcium levels from baseline. | Week 6 |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Study Site 1 | Nagoya | Japan |
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| ID | Term |
|---|---|
| D054559 | Hyperphosphatemia |
| ID | Term |
|---|---|
| D010760 | Phosphorus Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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| Placebo | Drug | oral administration |
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