Department of Dermatology and Allergology, Technical University of Munich, Munich, Germany.
Division of Internal Medicine, Asthma and Allergy, Barlicki University Hospital, Medical University of Lodz, Lodz, Poland.
J Allergy Clin Immunol. 2019 Mar;143(3):1058-1066.e6. doi: 10.1016/j.jaci.2018.12.1001. Epub 2019 Jan 15.
The SQ tree sublingual immunotherapy (SLIT)-tablet (ALK-Abelló, Hørsholm, Denmark) is developed for treatment of tree pollen-induced allergic rhinoconjunctivitis (ARC).
The aim of this pivotal phase III trial was to demonstrate the efficacy and safety of the SQ tree SLIT-tablet.
This was a randomized, double-blind, placebo-controlled trial with 634 subjects (12-65 years) with moderate-to-severe ARC despite use of symptom-relieving medication. Eligible subjects were randomized 1:1 to active or placebo treatment. The primary end point was the average daily ARC total combined score (TCS) during the birch pollen season (BPS) analyzed for subjects with diary data during the BPS. Secondary end points included average daily symptom scores (DSS) during the BPS, average TCS and DSS during the tree pollen season (TPS), and average daily medication scores (DMS) in the BPS and TPS.
The primary and key secondary end points demonstrated statistically significant and clinically relevant effects of the SQ tree SLIT-tablet compared with placebo. For the BPS, absolute (relative) differences from placebo were 3.02 (40%) for TCS, 1.32 (37%) for DSS, and 1.58 (49%) for DMS (all P < .0001). For the TPS, absolute (relative) differences from placebo were 2.27 (37%) for TCS, 0.99 (33%) for DSS, and 1.20 (47%) for DMS (all P < .0001). Treatment was well tolerated. The most frequently reported treatment-related adverse events were mild or moderate local reactions related to sublingual administration.
The trial demonstrated the efficacy and safety of the SQ tree SLIT-tablet compared with placebo during the BPS and TPS in adolescents and adults with birch pollen-induced ARC (EudraCT 2015-004821-15).
树花粉舌下免疫治疗(SLIT)-片剂(ALK-Abelló,Hørsholm,丹麦)用于治疗树木花粉引起的过敏性鼻结膜炎(ARC)。
本关键性 III 期试验旨在证明 SQ 树 SLIT 片剂的疗效和安全性。
这是一项随机、双盲、安慰剂对照试验,共纳入 634 例(12-65 岁)中度至重度 ARC 患者(尽管使用了缓解症状的药物)。合格的受试者以 1:1 的比例随机分为活性治疗或安慰剂治疗组。主要终点是桦树花粉季节(BPS)期间的平均每日 ARC 总综合评分(TCS),该评分基于 BPS 期间有日记数据的受试者进行分析。次要终点包括 BPS 期间的平均每日症状评分(DSS)、TCS 和 DSS 在树木花粉季节(TPS)期间的平均值,以及 BPS 和 TPS 期间的平均每日用药评分(DMS)。
与安慰剂相比,SQ 树 SLIT 片剂在主要和关键次要终点均显示出具有统计学意义和临床相关的疗效。对于 BPS,与安慰剂相比,TCS 的绝对(相对)差异为 3.02(40%),DSS 为 1.32(37%),DMS 为 1.58(49%)(均 P<.0001)。对于 TPS,与安慰剂相比,TCS 的绝对(相对)差异为 2.27(37%),DSS 为 0.99(33%),DMS 为 1.20(47%)(均 P<.0001)。治疗耐受性良好。最常报告的与治疗相关的不良事件是与舌下给药相关的轻度或中度局部反应。
与安慰剂相比,在青少年和成人中,桦树花粉引起的 ARC 患者中,该试验证明了 SQ 树 SLIT 片剂在 BPS 和 TPS 期间的疗效和安全性(EudraCT 2015-004821-15)。