Pharmacokinetics and Pharmacodynamics of <scp>KT</scp>‐474, a Novel Selective Interleukin‐1 Receptor–Associated Kinase 4 (<scp>IRAK4</scp>) Degrader, in Healthy Adults
Sagar Agarwal, Alice McDonald, Veronica T. Campbell, Dapeng Chen, J. E. Davis, Haojing Rong, Aimee Mishkin, Anthony Slavin, Ashwin Gollerkeri, Jared Gollob
Abstract
Interleukin-1 receptor-associated kinase 4 (IRAK4), a key component of the Myddosome complex, mediates signaling through toll-like and interleukin-1 receptors. KT-474, a heterobifunctional IRAK4 degrader, was evaluated in a randomized, double-blind, placebo-controlled Phase 1 trial (NCT04772885) in single (25, 75, 150, 300, 600, 1000, and 1600 mg) and multiple (25, 50, 100, and 200 mg once daily [QD] for 14 days; or 200 mg twice weekly) ascending doses in healthy subjects. The pharmacokinetics of KT-474 and its diastereomers, the pharmacodynamics of KT-474, and the effect of food on KT-474 pharmacokinetics and the pharmacokinetic-pharmacodynamic analysis are presented as additional analyses to supplement the Ackerman et al. publication. KT-474 showed delayed absorption and prolonged elimination. Plasma exposure increased less than dose-proportionally, with single-dose exposure plateauing after the 1000 mg dose. Steady state was achieved after 7 days of daily dosing and resulted in a 3- to 4-fold accumulation in exposure. A significant food effect was observed at the 600 mg dose, with exposure increasing up to 2.57-fold when KT-474 was administered with a high-fat meal. Urinary excretion of KT-474 was < 1%. KT-474 demonstrated robust IRAK4 degradation in blood, with mean reductions of up to 98% observed at the 50-200 mg QD doses, as well as inhibition of ex vivo induction of a broad array of cytokines and chemokines by stimulants lipopolysaccharides and R848. Analysis of the relationship between plasma KT-474 concentration and IRAK4 reduction in blood indicated that plasma concentrations of 4.1-5.3 ng/mL would yield 80% IRAK4 reductions.