Effect of Phosphate Binders and a Dietary Iron Supplement on the Pharmacokinetics of a Single Dose of Vadadustat in Healthy Adults

• Published in: Clinical pharmacology in drug development Vol. 11; no. 4; pp. 475 - 485
• Main Authors: Paulson, Susan K., Martinez, Jimena, Sawant, Rishikesh, Burke, Steven K., Chavan, Ajit
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.04.2022; John Wiley and Sons Inc
• Subjects: Adult; Anemia; clinical trials; Drug dosages; drug metabolism; drug‐drug interactions; Female; Glycine - analogs & derivatives; Humans; Iron; Iron, Dietary; Kidney diseases; Male; nephrology; Original; Pharmacokinetics; Phosphates; Picolinic Acids; renal disease; nephrology; pharmacokinetics; drug-drug interactions; clinical trials; renal disease; drug metabolism
• ISSN: 2160-763X; 2160-7648
• DOI: 10.1002/cpdd.1033

Vadadustat is a hypoxia‐inducible factor prolyl‐hydroxylase inhibitor being developed for the treatment of anemia in patients with chronic kidney disease. Sequelae of chronic kidney disease include hyperphosphatemia and anemia, which are frequently treated with phosphate binders and iron supplements, respectively. Two studies evaluating the pharmacokinetics, safety, and tolerability of a single oral dose of vadadustat coadministered with a phosphate binder or iron supplement were conducted in healthy adult participants. In study 1, 54 healthy women and men were administered vadadustat (300 mg) alone and 1 hour before, concurrently with, or 2 hours after a phosphate binder (sevelamer carbonate 1600 mg, calcium acetate 1334 mg, or ferric citrate 2000 mg). In study 2, 10 healthy men were administered vadadustat (450 mg) alone and concomitantly with the oral iron supplement ferrous sulfate (325 mg [equivalent to 65 mg of elemental iron]). Vadadustat exposure was reduced by coadministration with sevelamer carbonate, calcium acetate, ferric citrate, or ferrous sulfate. Geometric least squares mean ratios for area under the concentration‐time curve from time 0 to infinity were reduced 37% to 55% by phosphate binders and 46% by ferrous sulfate. However, when vadadustat was administered 1 hour before phosphate binders, 90% confidence intervals for vadadustat exposure were within the no‐effect boundaries of +50% to –33%, indicating that drug‐drug interactions can be reduced by administering vadadustat 1 hour before phosphate binders. Vadadustat was well tolerated when administered in conjunction with phosphate binders or an iron supplement.