Trial ID: | L1129 |
Source ID: | NCT03988920
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Associated Drug: |
Tenapanor
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Title: |
A Long-Term Study of Tenapanor Alone or in Combination With Sevelamer in Patients With CKD on Dialysis and HP
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Acronym: |
NORMALIZE
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Status: |
COMPLETED
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Study Results: |
YES
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Results: |
https://ClinicalTrials.gov/show/NCT03988920/results
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Conditions: |
Hyperphosphatemia|End Stage Renal Disease
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Interventions: |
DRUG: Tenapanor|DRUG: Sevelamer Carbonate
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Outcome Measures: |
Primary: Achieving Normal Serum Phosphorus Level, Proportion of patients with serum phosphorus between 2.5 and 4.5 mg/dL, 18 months | Secondary: Change in Serum Phosphorus (s-P) From TEN-02-301 (Parent Study) Baseline, The change from the baseline s-P from the parent study until the endpoint visit which was up to 2.5 years after the baseline, up to 2.5 years|Change From Baseline in Serum Phosphorus (of Extension Study; TEN-02-401) to Endpoint Visit, Baseline upon enrollment in the 18-month long-term extension study, up to 18 months
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Sponsor/Collaborators: |
Sponsor: Ardelyx
|
Gender: |
ALL
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Age: |
CHILD, ADULT, OLDER_ADULT
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Phases: |
PHASE4
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Enrollment: |
172
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Study Type: |
INTERVENTIONAL
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Study Designs: |
Allocation: NON_RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
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Start Date: |
2019-06-15
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Completion Date: |
2021-07-31
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Results First Posted: |
2023-03-29
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Last Update Posted: |
2023-03-29
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Locations: |
Ardelyx Site #509, Houston, California, 77099, United States
|
URL: |
https://clinicaltrials.gov/show/NCT03988920
|