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延长慢性自发性荨麻疹患者奥马珠单抗治疗间隔时间(EXOTIC):一项多中心、随机、开放标签、非劣效性试验方案

EXtending Omalizumab Treatment Intervals in patients with Chronic spontaneous urticaria (EXOTIC): protocol of a multicentre, randomised, open-label, non-inferiority trial.

作者信息

Zhang Ditte Georgina, Sørensen Jennifer Astrup, Ghazanfar Misbah Noshela, Ali Zarqa, Vestergaard Christian, Thyssen Jacob, Egeberg Alexander, Thomsen Simon Francis

机构信息

Department of Dermatology, Bispebjerg Hospital, Copenhagen, Denmark

Department of Dermatology, Bispebjerg Hospital, Copenhagen, Denmark.

出版信息

BMJ Open. 2025 Jan 6;15(1):e084987. doi: 10.1136/bmjopen-2024-084987.

Abstract

INTRODUCTION

Omalizumab, an anti-IgE monoclonal antibody, is effective in treating antihistamine-refractory chronic spontaneous urticaria (CSU). However, tapering strategies for omalizumab are currently not well-studied, and patients may be treated longer than needed. Here, we present the rationale and design of the EXtending Omalizumab Treatment Intervals in patients with Chronic spontaneous urticaria trial, a multicentre, randomised, open-label, non-inferiority clinical trial. The objective of this trial is to investigate if patients with well-controlled CSU, achieved by standard treatment of 300 mg omalizumab administered subcutaneously every 4 weeks (Q4W) for 12 weeks, can maintain disease control with every 6 weeks (Q6W) dosing interval.

METHODS AND ANALYSIS

Participants who achieve an Urticaria Control Test (UCT) score ≥12 after 12 weeks on omalizumab will be randomised to 300 mg omalizumab treatment Q4W or Q6W. Treatment arms will be followed for a total of 36 weeks. The primary endpoint is the absolute difference in average UCT score between treatment arms at week 36. Blood samples, Weekly Urticaria Activity Score, Chronic Urticaria Quality of Life Questionnaire, Dermatology Life Quality Index and records of side effects and flares will be obtained throughout the study at weeks 0, 12, 24 and 36.

ETHICS AND DISSEMINATION

The study has been approved by the Scientific Ethical Committee of the Capital Region in Denmark, the local Data Protection Agency and the Danish Medicines Agency. All study participants must provide written informed consent. The study will be conducted according to the Helsinki Declaration and Good Clinical Practice. Findings will be disseminated through publication in peer-reviewed journals and presented at international conferences.

TRIAL REGISTRATION NUMBER

EU CT no. 2023-506187-14-00, ClinicalTrials.gov: NCT05916937.

摘要

引言

奥马珠单抗是一种抗IgE单克隆抗体,对治疗抗组胺药难治性慢性自发性荨麻疹(CSU)有效。然而,目前对奥马珠单抗的减药策略研究不足,患者可能接受了比所需时间更长的治疗。在此,我们介绍慢性自发性荨麻疹患者延长奥马珠单抗治疗间隔试验的基本原理和设计,这是一项多中心、随机、开放标签、非劣效性临床试验。该试验的目的是研究通过每4周皮下注射300mg奥马珠单抗标准治疗12周实现病情良好控制的CSU患者,是否可以通过每6周给药间隔维持病情控制。

方法与分析

在接受奥马珠单抗治疗12周后荨麻疹控制测试(UCT)评分≥12的参与者将被随机分为每4周或每6周接受300mg奥马珠单抗治疗。治疗组将总共随访36周。主要终点是第36周时治疗组之间平均UCT评分的绝对差异。在研究的第0、12、24和36周将采集血样、每周荨麻疹活动评分、慢性荨麻疹生活质量问卷、皮肤病生活质量指数以及副作用和皮疹发作记录。

伦理与传播

该研究已获得丹麦首都地区科学伦理委员会、当地数据保护机构和丹麦药品管理局的批准。所有研究参与者必须提供书面知情同意书。该研究将按照《赫尔辛基宣言》和良好临床实践进行。研究结果将通过在同行评审期刊上发表以及在国际会议上展示进行传播。

试验注册号

欧盟临床试验编号2023 - 506187 - 14 - 00,ClinicalTrials.gov:NCT05916937。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e35/11749435/b75b96be53da/bmjopen-15-1-g001.jpg

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