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To investigate the safety of repeated administration of KHK7791 for 52 weeks while switching from a phosphate-binding agent to KHK7791 in Hemodialysis patients with hyperphosphatemia.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| KHK7791 | Experimental | During the dosing period, subjects administer KHK7791 twice daily just before meals.Subjects will be underwent tests at scheduled visits at least weekly until Week 12, at least once every 2 weeks after completion of Week 12 test. KHK7791 and phosphate binders are adjusted with the goal of controlling serum phosphorus concentration within a certain range based on the dose adjustment criteria described in the study protocol.It should be considered that phosphorus adsorbent should be switched to KHK7791 whenever feasible. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| KHK7791 | Drug | oral administration |
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| Measure | Description | Time Frame |
|---|---|---|
| Incidence rates of all adverse events and adverse drug reactions that occurred or worsened after the initiation of KHK7791 treatment for 52 weeks. | To investigate the safety of repeated administration of KHK7791 for 52 weeks while switching from a phosphate-binding agent to KHK7791 in Hemodialysis patients with hyperphosphatemia. | Dose period Week 1~52 |
| Measure | Description | Time Frame |
|---|---|---|
| Achievement of at least 30% change of the total number of daily prescription tablets of phosphorus binders and KHK7791 from baseline in the last 3 weeks of the final assessment. | To investigate the efficacy of repeated administration of KHK7791 for 52 weeks while switching from a phosphate-binding agent to KHK7791 in hyperphosphatemic subjects undergoing hemodialysis. Important secondary endpoint |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Medical Corporation Seijinkai Ikeda Hospital | Kanoya | Kagoshima-ken | Japan |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 42387036 | Derived | Nagano N, Tokunaga S, Asada S, Fukagawa M, Akizawa T. Tenapanor reduces phosphate binder pill burden among hemodialysis patients in a post hoc phase 3 analysis. Sci Rep. 2026 Jul 1. doi: 10.1038/s41598-026-58594-9. Online ahead of print. | |
| 37925471 | Derived | Koiwa F, Sato Y, Ohara M, Nakanishi K, Fukagawa M, Akizawa T. Long-term safety and decrease of pill burden by tenapanor therapy: a phase 3 open-label study in hemodialysis patients with hyperphosphatemia. Sci Rep. 2023 Nov 4;13(1):19100. doi: 10.1038/s41598-023-45080-9. |
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The datasets generated and/or analyzed during the study sponsored by Kyowa Kirin will be available in the Vivli repository, https://vivli.org/ourmember/kyowa-kirin/ as long as conditions of data disclosure specified in the policy section of the Vivli website are satisfied.
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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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| Week 1~52 |
| Total daily prescription of phosphate binders and KHK7791 tablets, such as tablet counts, at each time point after the start of treatment. | Week 1~52 |
| Achievement of at least 30% change of the total number of daily prescription tablets of phosphorus binders and KHK7791 from baseline, at each time point after the start of treatment. | Week 1~52 |
| The change of total daily prescription of phosphate binders and KHK7791 tablets, such as tablet counts, at each time point after the start of treatment. | Week 1~52 |
| The rate of change of total daily prescription of phosphate binders and KHK7791 tablets, such as tablet counts, at each time point after the start of treatment. | Week 1~52 |
| Concentration of serum phosphorous levels values at each time point. | Week 1~52 |
| Change of serum phosphorous levels from baseline values at each time point. | Week 1~52 |
| Achievement/failure of the target serum phosphorus level (serum phosphorus level: ≤ 6.0). | Week 1~52 |
| Time when the target serum phosphorus level (serum phosphorus level: ≤ 6.0) was achieved. | Week 1~52 |
| Achievement/failure of the target serum phosphorus level (serum phosphorus level: ≤ 5.5). | Week 1~52 |
| Time when the target serum phosphorus level (serum phosphorus level: ≤ 5.5) was achieved. | Week 1~52 |
| Concentrations of such as Ca × P product levels at each time point. | Week 1~52 |
| Changes of such as Ca × P product levels from baseline values at each time point. | Week 1~52 |