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Barrier-forming, drug-free nasal spray reduces allergic symptoms induced by house dust mite allergen.
Couroux, Patricia; Grosse, Nicole; Salapatek, Anne Marie; Goyal, Yasmeen; Pfaar, Oliver; Hohenfeld, Ilja P.
Afiliação
  • Couroux P; Inflamax Research DBA Cliantha Research, Mississauga, Ontario, Canada.
  • Grosse N; Altamira Medica AG, Zug, Switzerland.
  • Salapatek AM; Inflamax Research DBA Cliantha Research, Mississauga, Ontario, Canada.
  • Goyal Y; Inflamax Research DBA Cliantha Research, Mississauga, Ontario, Canada.
  • Pfaar O; Department of Otorhinolaryngology, Head and Neck Surgery, Section of Rhinology and Allergy, University Hospital Marburg, Philipps-Universität Marburg, Marburg, Germany.
  • Hohenfeld IP; Altamira Medica AG, Zug, Switzerland.
Clin Transl Allergy ; 13(7): e12277, 2023 Jul.
Article em En | MEDLINE | ID: mdl-37488728
ABSTRACT

BACKGROUND:

House Dust Mite (HDM) is the most common indoor allergen triggering allergic symptoms. First-line pharmacotherapy treatment is recommended in international guidelines, while the avoidance of allergens represents a still unmet guideline principle. AM-301 is a new non-pharmacological nasal spray that creates a protective gel-like barrier on the nasal mucosa, preventing the contact with the allergens.

METHODS:

This randomized, open-label, 3-period crossover study assessed the efficacy and safety of AM-301. The objective was to determine whether AM-301 reduces allergic rhinitis (AR) symptoms in patients exposed to HDM allergens. Adults with confirmed Perennial Allergic Rhinitis (PAR; n = 37) were exposed to HDM allergen in a controlled Allergen Exposure Chamber before and during a treatment course of AM-301 (in six different sequences) within 3 weeks (A One spray AM-301 per nostril/B Two sprays AM-301 per nostril/C no treatment). For the primary efficacy analysis, data from the total nasal symptom score (TNSS) were pooled from treatment A + B (D) and analyzed with Analysis of Covariance Model. As secondary endpoints, single time points, visits and symptoms were analyzed.

RESULTS:

The primary endpoint (overall change in TNSS from baseline over all three visits) showed significant results (p = 0.0085). A comparable alleviation of all four symptoms (itchy nose, nasal congestion, runny nose, sneezing) by the protective layer started to emerge after 40 min and lasted up to 180 min (end of challenge). AM-301 resulted to be safe and well-tolerated.

CONCLUSION:

AM-301 significantly reduced HDM-related allergic symptoms in a standardized allergen challenge. Protection was observed to last up to 180 min.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Idioma: En Revista: Clin Transl Allergy Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Idioma: En Revista: Clin Transl Allergy Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá