Key result
A 2-compartment pharmacokinetic model showed that formulation, weight, and age were significant covariates for LY2623091 disposition, while hypertension and CKD status were not.
Why the study?
What are the population pharmacokinetics and significant covariates affecting the disposition of LY2623091 in healthy subjects and patients with hypertension and/or CKD?
What are the population pharmacokinetics and significant covariates affecting the disposition of LY2623091 in healthy subjects and patients with hypertension and/or CKD?
Answers are grounded in this paper and cite their sources.
The pharmacokinetics of the novel nonsteroidal MRA LY2623091 are not significantly altered by hypertension or CKD, suggesting dose adjustments may not be necessary for these conditions.
LY2623091 is a selective, orally active, nonsteroidal, competitive mineralocorticoid receptor antagonist that blocks the actions of aldosterone and other mineralocorticoid receptor ligands at the receptor level. The aim of this work was to explore and establish a population pharmacokinetic model, quantify the degree of interindividual variability, and identify significant disease-, patient-, and study-specific covariates that alter the disposition of LY2623091. The data included concentrations from 294 healthy subjects and patients with hypertension and/or chronic kidney disease (CKD), sampled in 5 phase 1 and 2 studies. The pharmacokinetics of LY2623091 was well described by a 2-compartment model with first-order absorption and elimination. Formulation (on oral bioavailability) as well as weight and age (both on apparent central volume of distribution) were found to be significant covariates. The relative bioavailability of the capsule formulation was 68.4% compared to that of the solution. Hypertension and CKD status were not significant covariates. The pharmacokinetic model suggests that given the same dose, patients with hypertension and/or CKD would receive a similar exposure compared to subjects without these disease conditions.
No takes yet. Share an insight, caveat, or question.
Wang et al. (2017) studied Hypertension and/or chronic kidney disease (n=294). LY2623091 was evaluated on Population pharmacokinetic model and significant covariates altering disposition. A 2-compartment pharmacokinetic model showed that formulation, weight, and age were significant covariates for LY2623091 disposition, while hypertension and CKD status were not.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: