Trial ID: | L0910 |
Source ID: | NCT03242967
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Associated Drug: |
Vadadustat
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Title: |
Study to Evaluate Three Times Per Week (TIW) Oral Dosing of Vadadustat for Anemia in Subjects With Dialysis-Dependent Chronic Kidney Disease (DD-CKD)
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Acronym: |
TRILOGY
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Status: |
WITHDRAWN
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Study Results: |
NO
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Results: |
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Conditions: |
Anemia|Dialysis-Dependent Chronic Kidney Disease
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Interventions: |
DRUG: Vadadustat|DRUG: Darbepoetin alfa
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Outcome Measures: |
Primary: Mean change in Hb between baseline and the primary evaluation period, Mean change in hemoglobin will be evaluated, Baseline visit, Week 36 | Secondary: Mean change in Hb between baseline and the secondary evaluation period, Mean change in hemoglobin will be evaluated, Baseline visit, Week 52|Proportion of subjects with mean Hb within the target range during the primary evaluation period, Hemoglobin values within the target range will be evaluated, Baseline visit, Week 36|Adverse Events (AEs) and Serious Adverse Events (SAEs), Adverse Events (AEs) and Serious Adverse Events (SAEs) will be evaluated, 52 weeks
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Sponsor/Collaborators: |
Sponsor: Akebia Therapeutics
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Gender: |
ALL
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Age: |
ADULT, OLDER_ADULT
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Phases: |
PHASE3
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Enrollment: |
0
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Study Type: |
INTERVENTIONAL
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Study Designs: |
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
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Start Date: |
2017-08
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Completion Date: |
2018-02-12
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Results First Posted: |
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Last Update Posted: |
2018-11-05
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Locations: |
Research Site, Northridge, California, 91324, United States
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URL: |
https://clinicaltrials.gov/show/NCT03242967
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