Exposure-response analysis of the efficacy and safety of esaxerenone, a novel nonsteroidal mineralocorticoid receptor blocker, in hypertensive patients with or without diabetic kidney disease

Drug Metab Pharmacokinet. 2024 Apr:55:100535. doi: 10.1016/j.dmpk.2023.100535. Epub 2023 Oct 19.

Abstract

Background: Esaxerenone is a novel non-steroidal mineralocorticoid receptor blocker. Here, we assessed efficacy and safety exposure-response relationships of esaxerenone and its covariates and thereby justified the recommended dosage regimens, focusing on the safety benefits of up-titration regimen in patients at higher risk for increased serum potassium (sK+).

Methods: The relationships between model-derived individual esaxerenone exposure and efficacy (blood pressure [BP]) and safety (increased sK+) were evaluated using multivariate linear regression and Cox regression analyses, respectively, using data from 1453 hypertensive patients with or without diabetic kidney disease in five clinical studies.

Results: Exposure-efficacy analyses demonstrated that higher exposure was linearly associated with greater BP reduction over the investigated dose range. Exposure-safety analyses showed that higher exposure was associated with a higher risk of increased sK+ under a fixed-dosing regimen; higher baseline sK+ and lower baseline estimated glomerular filtration rate (eGFR) were influential covariates. Model-based simulations suggested that fewer occurrences of increased sK+ are expected under the up-titration regimen (from 1.25 to 5 mg) relative to the fixed-dosing regimen (5 mg) in patients with different combinations of these covariates.

Conclusions: The exposure-response analyses supported the esaxerenone recommended doses and the safety benefits of using the up-titration regimen.

Keywords: Blood pressure; Esaxerenone; Exposure-response relationship; Hypertension; Non-steroidal mineralocorticoid receptor blocker; Serum potassium; Titration.

MeSH terms

  • Diabetes Mellitus* / chemically induced
  • Diabetic Nephropathies* / chemically induced
  • Diabetic Nephropathies* / drug therapy
  • Humans
  • Hypertension* / chemically induced
  • Hypertension* / drug therapy
  • Mineralocorticoid Receptor Antagonists / adverse effects
  • Pyrroles / adverse effects
  • Receptors, Mineralocorticoid
  • Sulfones*

Substances

  • esaxerenone
  • Receptors, Mineralocorticoid
  • Mineralocorticoid Receptor Antagonists
  • Pyrroles
  • Sulfones