Tolerability of the SQ Tree SLIT Tablet in Adults

被引:12
作者
Birk, Anne O. [1 ]
Andersen, Jens S. [1 ]
Villesen, Hanne H. [1 ]
Steffensen, Maria A. [1 ]
Calderon, Moises A. [2 ]
机构
[1] ALK, Global Pharmacovigilance & Clin Dev, Boge Alle 3, DK-2970 Horsholm, Denmark
[2] Imperial Coll London, Royal Brompton Hosp, Natl Heart & Lung Inst, London, England
关键词
allergic rhinoconjunctivitis; allergy immunotherapy; birch pollen; immunology; sublingual immunotherapy tablet; tolerability; POLLEN-INDUCED RHINOCONJUNCTIVITIS; TERM CLINICAL-EFFICACY; FOLLOW-UP; SUBLINGUAL IMMUNOTHERAPY; ALLERGY IMMUNOTHERAPY; ASTHMA; CHILDREN; PAT; PERSPECTIVE; PREVENTION;
D O I
10.1016/j.clinthera.2017.08.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: The tree pollen sublingual immunotherapy (SLIT)-tablet (ALK, Denmark) is being developed for the treatment of tree pollen induced allergic rhinitis with or without conjunctivitis. The objective of this Phase I trial was to investigate the tolerability and acceptable dose range of the SQ tree SLIT -tablet in adults with allergic rhinoconjunctivitis. Methods: The trial was a randomized, doubleblind, placebo-controlled, dose escalation Phase I trial that included 70 adults (aged 19-61 years) with birch pollen induced rhinoconjunctivitis with or without mild to moderate asthma. The trial included 6 different dosage groups that were randomized 3:1 to active treatment or placebo once daily for 28 days. Adverse events (AEs) were coded in the Medical Dictionary for Regulatory Activities by medically qualified personnel. Immunologic assessments included IgE and IgE-blocking factor. Findings: Most (96%) reported AEs were mild, and only 5 severe events (0.2%) were reported. The most frequently reported investigational medicinal product related AEs were oral pruritus, ear pruritus, mouth edema, sensation of foreign body, throat irritation, pharyngolaryngeal pain, dry throat, tongue blistering, eye pruritus, and headache. The trial included doses ranging from 1 to 24 development units (DU), and the mean number of investigational medicinal product related AEs per participant was highest in the 24 DU group. The 12 and 24 DU doses induced statistically significant changes from baseline compared with placebo in birch specific IgE and IgE-blocking factor. (C) 2017 Elsevier HS Journals, Inc. All rights reserved.
引用
收藏
页码:1858 / 1867
页数:10
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