Treatment with the SQ tree sublingual immunotherapy tablet is safe and well tolerated in real‐life

Author:

Pfaar Oliver1ORCID,Wolf Hendrik2ORCID,Reiber Rainer3ORCID,Knulst André4ORCID,Sidenius Kirsten56ORCID,Mäkelä Mika J.7ORCID,Steinsvåg Sverre8ORCID,Janson Christer9ORCID,van der Zwan Leonard10ORCID,Uss Elena10ORCID,Arvidsson Peter11ORCID,Borchert Kathrin12ORCID,Himmelhaus Helena12ORCID,Wüstenberg Eike213ORCID

Affiliation:

1. Department of Otorhinolaryngology, Head and Neck Surgery, Section of Rhinology and Allergy University Hospital Marburg Philipps‐Universität Marburg Marburg Germany

2. Medical Department/Clinical Development ALK‐Abelló Arzneimittel GmbH Hamburg Germany

3. Facharztpraxis für HNO/Allergologie Schorndorf Germany

4. Department of Dermatology/Allergology University Medical Center Utrecht Utrecht University Utrecht The Netherlands

5. Allergiklinikken i Bagsværd Bagsværd Denmark

6. Aleris Hospitaler København Søborg Denmark

7. Skin and Allergy Hospital HUS Helsinki University Hospital Helsinki Finland

8. Sørlandet Sykehus Kristiansand Norway

9. Department of Medical Sciences: Respiratory, Allergy and Sleep Research Uppsala University Uppsala Sweden

10. ALK‐Abelló Benelux Almere The Netherlands

11. ALK Nordic A/S Danmark filial Kungsbacka Sweden

12. Xcenda GmbH part of Cencora Hannover Germany

13. Department of Otorhinolaryngology Head and Neck Surgery Faculty of Medicine (and University Hospital) Carl Gustav Carus Technische Universität Dresden Dresden Germany

Abstract

AbstractBackgroundThe SQ tree sublingual immunotherapy (SLIT)‐tablet is authorised for treatment of allergic rhinoconjunctivitis with or without asthma in trees of the birch homologous group in 21 European countries. The primary objective of this study was to explore the safety in real‐life.MethodsIn a prospective, non‐interventional post‐authorisation safety study (EUPAS31470), adverse events (AEs) and adverse drug reactions (ADRs) at first administration and follow‐up visits, symptoms, medication use, and pollen food syndrome were recorded by physicians in 6 European countries during the first 4–6 months of treatment.ResultsADRs with the SQ tree SLIT‐tablet were reported in 57.7% of 1069 total patients (median age 36.0 years, 53.7% female) during the entire observation period (severity, mild‐to‐moderate: 70.1%, severe: 4.7%, serious: 0.7%) and in 45.9% after first administration. ADRs were not increased with pollen exposure at first administration. With coadministration of the SQ tree and grass SLIT‐tablet AEs were reported in 73.8% of patients and in 52.8% with the SQ tree SLIT‐tablet alone. Nasal and eye symptoms improved in 86.9% and 80.9% of patients and use of symptomatic medication in 76.0%. PFS with symptoms was reported in 43.0% of patients at baseline and in 4.3% at the individual last visit.ConclusionsThe results of this non‐interventional safety study with the SQ tree SLIT‐tablet confirm the safety profile from placebo‐controlled clinical trials and support effectiveness in real‐life according to the published efficacy data. Safety was not impaired by pollen exposure at first administration or co‐administration with other SLIT‐tablets.

Publisher

Wiley

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