Model‐Informed Dose Justifications of Posaconazole in Japanese Patients for Prophylaxis and Treatment Against Fungal Infection

Abstract Posaconazole is a globally approved broad‐spectrum triazole antifungal compound. In Japanese patients, posaconazole has identical dosing regimens as those approved globally for both tablet and intravenous formulations. This article aims to describe a model‐informed approach for dose justification of posaconazole in the Japanese population as either high‐risk patients with fungal infections (prophylaxis patients) or patients with fungal infections (treatment patients). A simultaneous population pharmacokinetic (PK) model for tablet and intravenous formulation was developed on the basis of a data set including Japanese data from healthy participants and treatment patients. The PK profiles and exposure distributions in Japanese patients were predicted and compared against foreign patients, that is, patients outside of Japan. Relationships between the post hoc posaconazole exposures and frequently observed clinical adverse events were evaluated. Although clinical trials for Japanese prophylaxis patients were not conducted, PK profiles in Japanese prophylaxis patients were predicted using the population PK model and demographic covariate information obtained from the published literature. Based upon the globally approved dosing regimen, posaconazole exposure distribution was predicted to be the highest in Japanese treatment patients, and generally similar between Japanese and foreign prophylaxis patients. Exposures in Japanese patients exceeded the efficacy target level (500 ng/mL). Safety profiles in Japanese treatment patients with the highest exposures were clinically acceptable without specific concerns to Japanese patients and appeared to have no relationship with posaconazole exposures. From PK, safety, and efficacy perspectives, the use of the same dosing regimen as in foreign patients was justified in Japanese prophylaxis and treatment patients..

Medienart:	E-Artikel

Erscheinungsjahr:	2023
Erschienen:	2023

Enthalten in:	Zur Gesamtaufnahme - volume:63
Enthalten in:	The Journal of Clinical Pharmacology - 63(2023), 4, Seite 421-434

Beteiligte Personen:	Iwasa, Takashi [VerfasserIn] Almeida, Camila [VerfasserIn] Fauchet, Floris [VerfasserIn] Winchell, Gregory A. [VerfasserIn] Greef, Rik [VerfasserIn] Hasegawa, Chihiro [VerfasserIn] Yoshitsugu, Hiroyuki [VerfasserIn] Wrishko, Rebecca Ellen [VerfasserIn]

Anmerkungen:	© 2023, The American College of Clinical Pharmacology.

Umfang:	14

doi:	10.1002/jcph.2180

funding:
Förderinstitution / Projekttitel:

PPN (Katalog-ID):	WLY016075838