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Calendar

2024-11-14 Quarterly Report 2024-Q3
2024-08-23 Quarterly Report 2024-Q2
2024-05-03 Quarterly Report 2024-Q1
2024-03-15 Ex-date Ordinary Dividend ALK B 0.00 DKK
2024-03-14 Annual General meeting
2024-02-08 Year-end Report 2023
2023-11-15 Quarterly Report 2023-Q3
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2022-03-28 Split ALK B 1:20
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2022-02-08 Year-end Report 2021
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2021-03-18 Annual General meeting
2021-02-10 Year-end Report 2020
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2020-03-11 Annual General meeting
2020-02-05 Year-end Report 2019
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2017-03-15 Annual General meeting
2017-02-07 Year-end Report 2016
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2015-02-09 Year-end Report 2014
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2013-02-05 Year-end Report 2012
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2012-03-27 Annual General meeting
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2011-04-01 Annual General meeting
2010-03-29 Ex-date Ordinary Dividend ALK B 5.00 DKK

Description

CountryDenmark
ListLarge Cap Copenhagen
SectorHealth care
IndustryMedical technology
AlK-Abelló är verksamt inom läkemedelsbranschen. Bolaget är en utvecklare av allergi- och immunterapi. Verksamhet innehas på global nivå och produkterna säljs både som vaccin och i tablettform. En stor del av verksamheten fokuserar mot forskning och utveckling inom nämnt arbetsområde, där bolaget aktivt arbetar med diagnostisering och behandling av återkommande allergibesvär. Bolaget grundades 1923 och har sitt huvudkontor i Hørsholm, Danmark.
2024-05-30 13:44:23

ALK (ALKB:DC / OMX: ALK B / AKBLF) today announced that the European regulatory filing for ITULAZAX® (tree sublingual allergy immunotherapy (SLIT) tablet) in young children has been accepted for review by the relevant health authorities. The European regulatory review process is anticipated to take up to nine months so that, subject to approval, the first market introductions in Europe could take place from the first half of 2025.

The data used in the European filing include results from a successfully completed Phase 3 clinical trial involving 952 children in Canada and Europe. The trial was a Phase 3, randomised, placebo-controlled trial to study the efficacy and safety of ITULAZAX® in children aged 5 to 17 with a clinical history of moderate to severe allergic rhinitis and/or conjunctivitis induced by pollen from birch trees and other trees in the birch homologous group. The trial achieved its primary endpoint confirming an overall improvement of 22% compared to placebo. Results were highly statistically significant.

ALK’s Executive Vice President of Research and Development, Henriette Mersebach, says: “I’m pleased that our registration application for ITULAZAX® for young children has been accepted for review, and we look forward to the dialogue with the European authorities. The results in children are robust and consistent with previous trial results and this filing represents an important step forward for our ability to transform the medical treatment of children with tree pollen allergy as well as for ALK’s long-term growth ambitions.

Globally, it is estimated that more than 10 million children have uncontrolled respiratory allergies, and the number is growing. Tree pollen is a common cause of these uncontrolled allergies. In Europe, the ITULAZAX® tablet is currently approved for treatment of patients aged 18-65.

ALK-Abelló A/S

For further information, please contact:

Investor Relations: Per Plotnikof, tel. +45 2261 2525

Media: Maiken Riise Andersen, tel. +45 5054 1434

About ALK
ALK is a global specialty pharmaceutical company focused on allergy and allergic asthma. It markets allergy immunotherapy treatments and other products and services for people with allergy and allergy doctors. Headquartered in Hørsholm, Denmark, ALK employs around 2,800 people worldwide and is listed on Nasdaq Copenhagen. Find more information at www.alk.net.