Study to Assess the Safety and Pharmacokinetics of AKB-6548 in Participants With Chronic Kidney Disease (CKD), Stages 3 and 4

Completed · Phase 2

Conditions studied: Chronic Kidney Disease

In brief

This study was conducted to assess the pharmacokinetic (PK) profile, safety, and tolerability in participants with Stage 3 and 4 Chronic Kidney Disease (CKD) following a single oral dose of Vadadustat.

Key facts

Study ID

NCT04707573

Run by

Akebia Therapeutics

People needed

22

Starts

2010-07-08

Expected to finish

2010-09-24

Last updated by the study team

2022-06-28

Who can join

Age: 18 and older, up to 79. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 to 79 years of age, inclusive
• Chronic Kidney Disease Stage 3 (Estimated Glomerular Filtration Rate [eGFR] 30 to 59 milliliters [mL]/minute) or Stage 4 participants (eGFR of <30 mL/minute that were not yet on dialysis). eGFR was calculated using the Modification of Diet in Renal Disease (MDRD).
• Hemoglobin (Hb) <13.5 grams per deciliter (g/dL) except for Polycystic Kidney Disease (PKD) participants, in which Hb was to be ≤14 g/dL
• Transferrin saturation (TSAT) >12% and complete blood count (CBC) indicating normocytic red blood cell morphology, unless the medical monitor and investigator agreed that the participant was appropriate for this study
• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤1.8 x upper limit of normal (ULN)
• Alkaline phosphatase ≤2 x ULN
• Bilirubin ≤1.5 x ULN
• Female participants were not pregnant or breastfeeding. Women of childbearing potential agreed to use an acceptable method of contraception.
• Non-vasectomized male participants agreed to use an acceptable method of contraception
• Understood the procedures and requirements of the study and provided written informed consent and authorization for protected health information disclosure

You may not qualify if…

• Any medical or psychological condition that in the opinion of the Investigator would have interfered with the participant's ability to provide informed consent or comply with study instructions
• Any clinically significant or uncontrolled medical condition that in the opinion of the Investigator would have placed the participant at undo risk or would have compromised the interpretability of the findings in this study
• A body mass index (BMI) of greater than 40
• Seropositive for human immunodeficiency virus (HIV) or Hepatitis B surface antigen
• Seropositive for Hepatitis C virus (HCV) antibodies unless ALT, AST, bilirubin tests were within normal limits
• History of chronic liver disease
• Uncontrolled hypertension (diastolic blood pressure [BP] > 110 millimeters of mercury [mm Hg] or systolic BP >190 mm Hg at screening)
• New York Heart Association Class III or IV congestive heart failure
• Myocardial infarction, acute coronary syndrome, or stroke within 6 months of dosing
• History of myelodysplastic syndrome
• Participants known to have diabetic gastroparesis that was either symptomatic on therapy or was refractory to therapy
• Any history of malignancy in the previous 5 years except for curatively resected basal cell carcinoma of skin, squamous cell carcinoma of skin, cervical carcinoma in situ, or resected benign colonic polyps
• Evidence of active infection unless the medical monitor and investigator agreed that the participant was appropriate for this study
• History of rheumatoid arthritis or systemic lupus erythematosus (SLE) (History of osteoarthritis or gout did not exclude participants from eligibility in the study.)
• Age-related macular degeneration (AMD), diabetic macular edema or active diabetic proliferative retinopathy that was likely to require treatment during the trial
• History of deep vein thrombosis (DVT) that required active treatment. Superficial thrombosis was not excluded.
• History of ongoing hemolysis or diagnosis of hemolytic syndrome
• Known history of bone marrow fibrosis
• History of hemosiderosis or hemochromatosis
• Androgen therapy within 21 days from the last injection
• Red blood cell transfusion within 12 weeks
• Therapy with an erythropoiesis stimulating agent (ESA) such as human recombinant erythropoietin within the past 21 days
• Intravenous iron supplementation within the past 21 days
• Currently taking acetaminophen > 2.6 grams/day
• History of prior organ transplantation, or stem cell or bone marrow transplantation

Where it is running

• Research Site — Saint Paul, Minnesota, United States
• Research Site — Knoxville, Tennessee, United States

Full record on ClinicalTrials.gov

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