» Articles » PMID: 21257798

The Pharmacokinetics, Pharmacodynamics, and Safety of Orally Dosed INCB018424 Phosphate in Healthy Volunteers

Overview
Publisher Wiley
Specialty Pharmacology
Date 2011 Jan 25
PMID 21257798
Citations 72
Authors
Affiliations
Soon will be listed here.
Abstract

INCB018424 phosphate, a potent inhibitor of JAK enzymes with selectivity for JAK1&2, is in development for the treatment of myelofibrosis (MF). The oral dose pharmacokinetics, pharmacodynamics, safety, and tolerability of INCB018424 were evaluated in healthy volunteers in 2 double-blind, randomized, and placebo-controlled studies. The first study evaluated single ascending doses of 5 to 200 mg INCB018424 and the effect of food, whereas the second study evaluated multiple ascending doses, including both once- and twice-daily dosing for 10 days. As a Biopharma-ceutical Classification System class I drug, INCB018424 exhibited good oral bioavailability and dose-proportional systemic exposures. INCB018424 showed low oral dose clearance and a small volume of distribution, with an approximate 3-hour plasma half-life and insignificant accumulation following repeat dosing. A high-fat meal reduced INCB018424 C(max) by 24% but had little effect on INCB018424 AUC. INCB018424 was cleared primarily by metabolism with negligible renal excretion. The pharmacodynamics of INCB018424, evaluated by the inhibition of phosphorylated STAT3 following cytokine stimulation in whole blood, showed good correlation with INCB018424 plasma concentrations. INCB018424 was generally safe and well tolerated, with 25 mg bid and 100 mg qd established as the maximum tolerated doses in healthy volunteers.

Citing Articles

Ruxolitinib plus steroids for acute graft versus host disease: a multicenter, randomized, phase 3 trial.

Dou L, Zhao Y, Yang J, Deng L, Wang N, Zhang X Signal Transduct Target Ther. 2024; 9(1):288.

PMID: 39438467 PMC: 11496732. DOI: 10.1038/s41392-024-01987-x.


Maintenance of hematopoietic stem cells by tyrosine-unphosphorylated STAT5 and JAK inhibition.

Williams M, Wang X, Bastos H, Grondys-Kotarba G, Wu Q, Jin S Blood Adv. 2024; 9(2):291-309.

PMID: 39374575 PMC: 7617191. DOI: 10.1182/bloodadvances.2024014046.


A Phase I Trial Evaluating the Addition of Lenalidomide to Patients with Relapsed/Refractory Multiple Myeloma Progressing on Ruxolitinib and Methylprednisolone.

Berenson J, Limon A, Rice S, Safaie T, Boccia R, Yang H Target Oncol. 2024; 19(3):343-357.

PMID: 38643346 DOI: 10.1007/s11523-024-01049-w.


A novel strategy to generate immunocytokines with activity-on-demand using small molecule inhibitors.

Rotta G, Gilardoni E, Ravazza D, Mock J, Seehusen F, Elsayed A EMBO Mol Med. 2024; 16(4):904-926.

PMID: 38448543 PMC: 11018789. DOI: 10.1038/s44321-024-00034-0.


Anti-inflammatory and biologic drugs for atopic dermatitis: a therapeutic approach in children and adolescents.

Caffarelli C, Giannetti A, Gianni G, Ricci G Front Med (Lausanne). 2023; 10:1214963.

PMID: 37654660 PMC: 10466416. DOI: 10.3389/fmed.2023.1214963.