ALK's ITULAZAX® Approved for Pediatric Allergy Treatment in Europe
ALK's ITULAZAX® Approved for Pediatric Allergy Treatment
ALK (ALKB.DC / OMX: ALK B) has exciting news! The recent approval of its tree pollen sublingual allergy immunotherapy tablet, ITULAZAX®, for children and adolescents aged five to 17 marks a significant step forward in allergy treatment options available in Europe. Health authorities across 17 EU countries have greenlighted this important therapeutic option aimed at helping young patients who suffer from tree pollen-induced respiratory allergies.
The Executive Vice President of Research and Development, Henriette Mersebach, expressed the company's enthusiasm about this development, stating, "We are very pleased with the European health authorities' approval which allows us to provide this important treatment option to children and adolescents whose lives are impaired by uncontrolled tree pollen-induced respiratory allergy. Today’s approval marks another significant milestone in our continuous efforts to make our respiratory tablets available to all age groups in all relevant markets."
Details About the Clinical Trial
The approval was based on substantial clinical evidence gathered during the TT-06 clinical trial, a rigorous and randomized investigator's study. This trial involved 952 young participants aged five to 17 who had moderate to severe allergic reactions influenced by tree pollen, notably from birch trees. The research findings confirmed that ITULAZAX® was well tolerated by the majority of its young users and demonstrated a positive safety profile. Excitingly, these peer-reviewed research results were published in a well-respected medical journal.
Market Impact and Future Availability
Since its initial launch, the tree pollen tablet branded as ITULAZAX® in Europe and ITULATEK® in Canada had already gained approval in 22 countries specifically targeting adults aged 18 to 65. Reviews for pediatric use of this therapy are currently underway in Canada, Switzerland, and the UK, with the anticipation of completion in the near future.
The recent approval of ITULAZAX® not only fulfills a decade of continuous development but also ensures a comprehensive solution for five of the most common respiratory allergies. These include treatment options for grass pollen, house dust mite, ragweed pollen, Japanese cedar pollen, in addition to the newly approved tree pollen allergies, catering to children, teenagers, and adults alike.
Despite this incredible advancement, ALK has disclosed that the approval of ITULAZAX® for pediatric use is not expected to significantly alter their financial outlook for 2025. This means that while they continue to expand treatment avenues for younger patients, their overarching business strategy remains stable and focused.
Company Contact Information
For more comprehensive details about this approval and other inquiries, interested parties are encouraged to reach out to ALK-Abelló A/S directly. Investor Relations can be contacted via Per Plotnikof at +45 4574 7527, or mobile at +45 2261 2525. For media inquiries, Maiken Riise Andersen is reachable at +45 5054 1434.
About ALK
ALK is a leading global specialty pharmaceutical company that focuses primarily on allergy treatments, including allergy immunotherapy ('AIT'). With its headquarters in Hørsholm, Denmark, ALK employs approximately 2,800 individuals worldwide and has a notable presence on Nasdaq Copenhagen. The company is dedicated to providing effective solutions for individuals suffering from allergies, ensuring they can access reliable therapies tailored to their specific needs.
Frequently Asked Questions
What is ITULAZAX®?
ITULAZAX® is a tree pollen allergy immunotherapy tablet designed for children and adolescents aged 5-17, approved in Europe for treating respiratory allergies.
How does the approval of ITULAZAX® benefit young patients?
This approval provides a new treatment avenue for children suffering from tree pollen-induced respiratory allergies, improving their quality of life.
What was the basis for the approval of ITULAZAX®?
The approval was based on data from the TT-06 clinical trial, which showed that the treatment was well tolerated and had a favorable safety profile.
Are there plans for ITULAZAX® approval in other countries?
Yes, pediatric regulatory reviews are ongoing for ITULAZAX® in Canada, Switzerland, and the UK, with completion expected in the near future.
How does this approval affect ALK's financial outlook?
ALK has stated that the approval of ITULAZAX® for pediatric use is not expected to change their financial outlook for 2025.
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