Phase 1 Maximal Use Pharmacokinetic Study of Tirbanibulin Ointment 1% in Subjects With Actinic Keratosis.
Autor: | Yavel R; TKL Research Inc., Fair Lawn, New Jersey, USA., Overcash JS; Velocity Clinical Research, San Diego, California, USA., Cutler D; Athenex Inc., Buffalo, New York, USA., Fang J; Athenex Inc., Buffalo, New York, USA., Zhi J; Athenex Inc., Buffalo, New York, USA. |
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Jazyk: | angličtina |
Zdroj: | Clinical pharmacology in drug development [Clin Pharmacol Drug Dev] 2022 Mar; Vol. 11 (3), pp. 397-405. Date of Electronic Publication: 2021 Nov 16. |
DOI: | 10.1002/cpdd.1041 |
Abstrakt: | Tirbanibulin is a novel tubulin polymerization and Src kinase signaling inhibitor. This study was designed to fully characterize tirbanibulin pharmacokinetics (PK) when applied topically under maximal use conditions. This was an open-label, parallel-group PK safety study of tirbanibulin ointment 1% applied to 25 cm 2 of the face or balding scalp in adults with actinic keratosis (AK). Eligible subjects self-applied tirbanibulin once-daily for 5 days. PK sampling occurred on days 1, 3 and 4 at 0 hour (before dosing), and on day 5 at prespecified time points up to 24 hours after application. Safety assessments included adverse events and local skin reactions were evaluated up to day 29. Eighteen subjects (face or scalp, n = 9 each) completed the study. Subjects were White (100%), of mean [range] age 66.4 [43-83] years, predominantly men (83.3%) with Fitzpatrick skin type I to III (94.4%); baseline AK lesion count, mean [range] 8.2 [6-14]. All subjects had quantifiable but low plasma concentrations of tirbanibulin. On day 5, overall mean (standard deviation) maximum concentration (C (© 2021, The American College of Clinical Pharmacology.) |
Databáze: | MEDLINE |
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