2020-11-09 08:30Press release

New study evaluates Airsonett TLA technology in the treatment of children with severe atopic eczema

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Airsonett announced today that the company’s novel and proprietary technology TLA (Tempera-ture-controlled Laminar Airflow) would be evaluated in the treatment of children with severe atopic eczema. Imperial College London UK will perform and sponsor the single centre, random-ized placebo-controlled study. The study is a result of the positive results already seen in the proof of concept study published in May 2018 (ref.1,2)

The primary objective is to assess the clinical efficacy of overnight treatment with the TLA device in

children and adolescents with chronic, moderate to severe atopic eczema. The primary endpoint is mean change of eczema severity EASI at week 12 compared to baseline. The study was initially scheduled to start in early 2020 but was delayed due to Covid-19. The first patients were enrolled in October 2020.

"We are excited to see the outcome of this study, hopefully confirming the good results in the previous proof of concept study. We often see promising improvements in eczema symptoms among many patients that receive TLA treatment for their allergic asthma “, says Anders Due-Boje, CEO of Airsonett.

“We are very pleased, that we are now finally able to go ahead and investigate if the TLA provides benefit to children with moderate to severe eczema” says Dr Claudia Gore, trial Chief Investigator at Imperial College London.

For more information:
Anders Due-Boje, CEO, Airsonett AB
Phone: +46 70 526 03 00
E-mail: anders.due-boje@airsonett.eu

About severe, uncontrolled asthma
Patients with severe, uncontrolled asthma treated according to Global Initiative for Asthma (GINA) step 4/5 account for approximately 3% of all patients with persistent asthma, according to recent population-based studies using administrative and prescribed databases, but account for a much larger share of asthma-related healthcare resource use and costs. Treatment alternatives for such patients include high-dose inhaled corticosteroids (ICS) and long-acting β2-antagonists (LABAs) and/or systematic corticosteroids. During the last decade, several new drugs for the treatment of severe asthma have been developed, and some of these drugs, such as anti-immunoglobulin E and anti-interleukin 5 have been included in Step 5 in the latest GINA recommendations. The costs for treatment with these biologics are however very high. Temperature-controlled laminar airflow (TLA) is an effective treatment for patients with severe, uncontrolled asthma. The use of TLA has shown cost-effectiveness according to National Institute for Health and Care Excellence (NICE) standards and the Swedish Dental and Pharmaceutical Benefits Agency, TLV, a central government agency whose remit is to determine whether a pharmaceutical product, medical device or dental care procedure shall be subsidized by the state.

References:

1: Effect of a novel temperature-controlled laminar airflow device on personal breathing zone aeroallergen exposure.

Gore RB, Boyle RJ, Gore C, Custovic A, Hanna H, Svensson P, Warner JO.

Indoor Air. 2015 Feb;25(1):36-44. doi: 10.1111/ina.12122. Epub 2014 Jun 10.

PMID: 24750266

2: Temperature-controlled laminar airflow (TLA) device in the treatment of children with severe atopic eczema: Open-label, proof-of-concept study.

Gore C, Gore RB, Fontanella S, Haider S, Custovic A.

Clin Exp Allergy. 2018 May;48(5):594-603. doi: 10.1111/cea.13105. Epub 2018 Mar 13.

PMID: 29383776


About Airsonett

Airsonett® är ett svenskt medicintekniskt företag som är ledande inom icke-farmakologisk behandling av patienter med allergisk svår, okontrollerad astma och eksem. Airsonett® Air4 är en icke-invasiv medicinsk utrustning för hembehandling baserad på den patenterade tekniken Temperatur-reglerat laminärt luftflöde (TLA). Behandling med Airsonett® Air4 medför drastisk minskning av allergener och andra luftburna partiklar i patientens andningszon under vila och sömn. Airsonett® Air4 rekommenderas av Socialstyrelsen och Barnläkarföreningen samt ingår sedan 2015 i Läkemedelsverkets riktlinjer för astmabehandling. Airsonett® Air4 är en CE-märkt medicinteknisk utrustning, Klass 1, avsedd att användas för lindring av symtom vid allergiska sjukdomar såsom allergisk astma och eksem. Den följer relevanta EU-direktiv gällande utformning, funktion, säkerhet, hälsokrav och har genomgått rigorös klinisk forskning så väl som hälsoekonomiska analyser. Airsonett® Air4 innehar ett 510(k) godkännande, klass II, från FDA. Bolagets huvudägare är SEB Venture Capital, Industrifonden och Magnus Lundberg. För ytterligare information, besök www.airsonett.se


Contacts

Head of Marketing
Andreas Arnkvist
CEO
Anders Due-Boje