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SQ屋尘螨舌下免疫治疗片剂在日本成年屋尘螨诱发过敏性哮喘患者中的安全性概况:一项随机、双盲、安慰剂对照的I期研究。

Safety profile of the SQ house dust mite sublingual immunotherapy-tablet in Japanese adult patients with house dust mite-induced allergic asthma: a randomized, double-blind, placebo-controlled phase I study.

作者信息

Okamiya Kazuhiro, Sekino Hisakuni, Azuma Ryuji, Kudo Minoru, Sakaguchi Miyuki, Nemoto Fumi, Muramatsu Naoki, Maekawa Yuriko, Tanaka Akihiko

机构信息

Torii Pharmaceutical Co. Ltd. , Tokyo , Japan.

Department of Internal Medicine, Sekino Hospital , Tokyo , Japan.

出版信息

J Asthma. 2019 Dec;56(12):1347-1355. doi: 10.1080/02770903.2018.1541353. Epub 2018 Nov 16.

Abstract

The SQ house dust mite (HDM) sublingual immunotherapy (SLIT)-tablet has demonstrated effective treatment of HDM-induced allergic asthma in patients 18 years or older in European trials. This study investigated its safety and immunology profile in Japanese adult patients with mild-to-moderate HDM-induced allergic asthma. In this randomized, double-blind, placebo-controlled study, 48 Japanese patients were randomly assigned to a daily treatment of SQ HDM SLIT-tablet or placebo (3:1) for 14 d with or without an up-dosing regimen. Active groups comprised 5000, 10,000 or 20,000 Japanese Allergy Unit (JAU) for 14 d, and the up-dosing group comprised 5,000 JAU in day 1-3, 10,000 JAU in day 4-7 and 20,000 JAU in day 8-14. No marked differences were observed in the incidence rate of adverse events (AEs) and their severity among active groups. The five most common investigational medicinal product (IMP)-related AEs were local events at the application site observed within 30 min after the intake of the SQ HDM SLIT-tablet. Although most events recovered within 1 h, mouth edema indicated a different profile of duration with more than 25% of the events lasting for more than 1 h. The SQ HDM SLIT-tablet of up to 20,000 JAU was well tolerated, and safety profile was acceptable for Japanese subjects with HDM-induced allergic asthma.

摘要

在欧洲的试验中,SQ屋尘螨(HDM)舌下免疫治疗(SLIT)片剂已证明对18岁及以上HDM诱发的过敏性哮喘患者有有效的治疗作用。本研究调查了其在日本轻度至中度HDM诱发的过敏性哮喘成年患者中的安全性和免疫学特征。在这项随机、双盲、安慰剂对照研究中,48名日本患者被随机分配接受SQ HDM SLIT片剂或安慰剂的每日治疗(3:1),为期14天,有或没有递增给药方案。活性组分别接受5000、10000或20000日本过敏单位(JAU)治疗14天,递增给药组在第1 - 3天接受5000 JAU,第4 - 7天接受10000 JAU,第8 - 14天接受20000 JAU。活性组之间不良事件(AE)的发生率及其严重程度未观察到明显差异。五种最常见的与研究用药品(IMP)相关的AE是在摄入SQ HDM SLIT片剂后30分钟内观察到的应用部位局部事件。虽然大多数事件在1小时内恢复,但口腔水肿显示出不同的持续时间特征,超过25%的事件持续超过1小时。高达20000 JAU的SQ HDM SLIT片剂耐受性良好,对于HDM诱发的过敏性哮喘的日本受试者,其安全性特征是可接受的。

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