학술논문

A Randomized, Active-controlled, Open-label, Comparative Study to Assess the Safety andEfficacy of Posaconazole in Japanese Subjects with Deep-seated Fungal Infection / 深在性真菌症の日本人患者を対象としたポサコナゾールの安全性および有効性を検討する無作為化,実薬対照,非盲検比較試験
Document Type
Journal Article
Source
日本医真菌学会雑誌 / Nihon Ishinkin Gakkai Zasshi. 2020, 61(1):1
Subject
Japanese patients
aspergillosis
mucormycosis
posaconazole
Language
Japanese
ISSN
2434-5229
2434-5237
Abstract
Background: Posaconazole (PSCZ) is a broad-spectrum azole antifungal drug that shows potent antifungal activity to filamentous fungi and yeast-like fungi including Mucorales.Objective and Method: A randomized, active-controlled, open-label, comparative study to assess the safety and efficacy of PSCZ in Japanese subjects with deep-seated fungal infection was conducted (MK-5592 Protocol 101, ClinicalTrials.gov Identifier: NCT02180165). Subjects with aspergillosis were randomized at 2:1 ratio to PSCZ (57 subjects) or voriconazole (VRCZ, 27) and subjects with mucormycosis were allocated to PSCZ (3), and received study therapy at a maximum of 84 days. The overall response was assessed at Day 42, Day 84, or the end of treatment, and adverse events were followed up to 14 days after the end of treatment.Results: The overall response rates were 40.0% (2/5) for PSCZ and 100.0% (3/3) for VRCZ in invasive aspergillosis (at Day 42), 58.3% (28/48) for PSCZ and 87.0% (20/23) for VRCZ in chronic pulmonary aspergillosis (at Day 84), and 100.0% (3/3) for PSCZ in mucormycosis (at end of treatment) respectively. The common drug-related adverse events were pyrexia (22.8%), hypokalemia (15.8%), hepatic function abnormality (14.0%), and hypertension (14.0%) in PSCZ; and photophobia (29.6%), visual impairment (14.8%), and hepatic function abnormality (14.8%) in VRCZ.Conclusion: PSCZ was shown to be safe and effective in Japanese patients with aspergillosis and mucormycosis, pointing to its usefulness against fungal infections with limited treatment choices in Japan.