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Clinical Trial Details

Trial ID: L0910
Source ID: NCT03242967
Associated Drug: Vadadustat
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)
Acronym: TRILOGY
Status: WITHDRAWN
Study Results: NO
Results:
Conditions: Anemia|Dialysis-Dependent Chronic Kidney Disease
Interventions: DRUG: Vadadustat|DRUG: Darbepoetin alfa
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
Sponsor/Collaborators: Sponsor: Akebia Therapeutics
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE3
Enrollment: 0
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2017-08
Completion Date: 2018-02-12
Results First Posted:
Last Update Posted: 2018-11-05
Locations: Research Site, Northridge, California, 91324, United States
URL: https://clinicaltrials.gov/show/NCT03242967