AI Article Synopsis

  • - Daprodustat is a drug that helps stimulate red blood cell production (erythropoiesis) by mimicking the body's response to low oxygen levels, making it a potential treatment for anemia related to chronic kidney disease (CKD).
  • - A study involving 64 healthy Japanese males tested two different tablet strengths of daprodustat to check if they were bioequivalent and how food impacted its absorption in the body.
  • - Results showed that the 2-mg and 4-mg daprodustat tablets were bioequivalent, and eating a standard meal did not significantly affect how the drug was processed in the body, with the drug being well tolerated among participants.

Article Abstract

Daprodustat is a prolyl hydroxylase inhibitor that stimulates erythropoiesis in a manner similar to the natural response to hypoxia, whereby inhibition of hypoxia inducible factor (HIF) prolyl-4-hydroxylases by daprodustat ultimately results in increased levels of HIF-responsive genes. Daprodustat is under development as an emerging new class of agents for the treatment of anemia associated with chronic kidney disease (CKD). This was a single-center, single-dose, open-label, randomized, 2-way crossover study in healthy Japanese male participants consisting of 2 parts. The primary objective was to evaluate the bioequivalence (BE) between daprodustat tablet strengths (part 1) and to evaluate the food effect on the pharmacokinetics (PK) of daprodustat (part 2). A total of 64 healthy Japanese male participants were enrolled; 52 participants were included in part 1 and 12 in part 2. BE was demonstrated between the daprodustat 2-mg tablet and the daprodustat 4-mg tablet. A standard CKD meal did not have a large effect on the PK parameters of daprodustat after a single oral dose of daprodustat 4 mg. Administration of single oral doses of daprodustat 4 mg was generally well tolerated in the healthy Japanese participants, and no new safety signals were identified without regard to food.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687240PMC
http://dx.doi.org/10.1002/cpdd.793DOI Listing

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