目的:设计一项临床试验,评估一种生物制剂在严重哮喘中的口服皮质类固醇节约作用

W. Busse, Millie Wang, J. Gibson, Mattis Gottlow, M. Braddock, G. Colice
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引用次数: 10

摘要

在一项IIb期研究中,对接受大剂量吸入皮质类固醇(ICS)和长效β2激动剂(LABA)治疗的严重不受控制哮喘患者给予抗il -13全人源单克隆抗体tralokinumab,可显著改善肺功能。由于许多使用ICS-LABA的严重哮喘患者仅通过附加口服皮质类固醇(OCS)才能实现症状控制,因此存在对保留OCS治疗策略的未满足需求。这项III期、随机、双盲、平行组、安慰剂对照的TROPOS (NCT02281357)研究将评估曲洛单抗在需要持续ICS-LABA和慢性维持OCS的严重哮喘患者中节省OCS的潜力。在初始筛选/评估期后,患者将被随机分配到曲罗单抗或安慰剂组,为期40周(12周诱导期、20周OCS降低期和8周维持期);患者将随访14周。
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TROPOS: designing a clinical trial to evaluate the oral corticosteroid-sparing effect of a biologic in severe asthma
In a Phase IIb study, administration of tralokinumab, an anti-IL-13, fully human monoclonal antibody, to patients with severe uncontrolled asthma treated with high-dose inhaled corticosteroid (ICS) and long-acting β2-agonists (LABA) significantly improved lung function. Since many patients with severe asthma using ICS-LABA only achieve symptom control with add-on oral corticosteroids (OCS), an unmet need for OCS-sparing treatment strategies exists. This Phase III, randomized, double-blind, parallel-group, placebo-controlled TROPOS (NCT02281357) study will evaluate the OCS-sparing potential of tralokinumab in patients with severe asthma requiring continuous ICS-LABA and chronic maintenance OCS. After an initial screening/assessment period, patients will be randomized to tralokinumab or placebo for 40 weeks (12-week induction, 20-week OCS reduction and 8-week maintenance phases); patients will be followed-up for 14 weeks.
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