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WKN: A3DHX9 | ISIN: DK0061802139 | Ticker-Symbol: 4AJ0
Tradegate
11.09.26 | 08:00
26,840 Euro
+2,29 % +0,600
Branche
Pharma
Aktienmarkt
Europa 600
1-Jahres-Chart
ALK-ABELLO A/S Chart 1 Jahr
5-Tage-Chart
ALK-ABELLO A/S 5-Tage-Chart
RealtimeGeldBriefZeit
26,04026,52013:05
26,12026,36011.09.

Aktuelle News zur ALK-ABELLO Aktie

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21.08.ALK Abello: Report on transactions with ALK-Abelló A/S B shares and associated securities by managerial staff1
20.08.ALK-Abelló A/S reports Q2 results1
20.08.ALK-Abelló Profit Climbs In Q25
20.08.ALK Abello: Six-month interim report (Q2) 2026 (unaudited)288ALK delivers 18% organic revenue growth with operating profit (EBIT) up 19% in Q2 ALK sustained strong momentum in Q2, with double-digit growth across all regions driven by sales of tablets and anaphylaxis...
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20.08.ALK Abello: ALK appoints Jacob Glenting as head of Global R&D191ALK announces the appointment of Jacob Glenting as new Executive Vice President (EVP) and head of Global R&D, effective 1 September 2026. This position has been vacant since February 2026. Jacob Glenting...
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20.08.ALK-Abelló: ALK appoints Jacob Glenting as head of Global R&D180ALK announces the appointment of Jacob Glenting as new Executive Vice President (EVP) and head of Global R&D, effective 1 September 2026. This position has been vacant since February 2026. Jacob Glenting...
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20.08.ALK-Abelló: Six-month interim report (Q2) 2026 (unaudited)301ALK delivers 18% organic revenue growth with operating profit (EBIT) up 19% in Q2 ALK sustained strong momentum in Q2, with double-digit growth across all regions driven by sales of tablets and anaphylaxis...
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14.08.ALK Abello: ALK's tree pollen and house dust mite tablets now recommended by NICE for paediatric treatment in the UK health system216ALK (ALKB:DC / Nasdaq Copenhagen: ALK B) today announced that the UK's National Institute for Health and Care Excellence (NICE) has recommended the company's tree pollen tablet (ITULAZAX) and house...
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13.08.ALK Abello: Invitation to the presentation of ALK's first six months (Q2) 2026 results on Thursday, 20 August 20261
05.08.ALK Abello: Market launch of the nasal adrenaline spray, neffy, for treatment of adults and children with severe allergies in Canada1
15.06.ALK Abello: EURneffy 1 mg approved in the UK as the first and only needle-free adrenaline treatment for young children (aged 4 and older, 15-30 kg) at risk of anaphylaxis272ALK announced that the Medicines and Healthcare products Regulatory Agency (MHRA) has granted marketing authorisation for EURneffy 1 mg, the first and only needle-free adrenaline treatment for anaphylaxis...
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11.06.ALK Abello: Anaphylaxis management is falling short in 2026 - EAACI data suggest EURneffy, the only needle-free nasal adrenaline spray, could help close the gap354Over half (54%) of adults at risk of anaphylaxis admit they have been without their adrenaline auto-injector (AAI) when needed-and nearly 40% do not carry one regularly (n=1,238).1HCP survey data...
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04.06.ALK Abello: ALK will present data on real world-use of nasal adrenaline and key learnings from 20 years with SLIT-tablets at EAACI 202610
01.06.ALK Abello: Report on transactions with ALK-Abelló A/S B shares and associated securities by managerial staff3
05.05.ALK-Abelló A/S reports Q1 results, raises guidance2
05.05.ALK-Abelló Profit Advances In Q13
04.05.ALK Abello: Three-month interim report (Q1) 2026 (unaudited)614ALK delivers 18% organic revenue growth with operating profit (EBIT) up 22% in Q1 Q1 saw broad-based growth across key categories and regions with sustained, strong momentum in tablet sales in Europe...
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04.05.ALK Abello: ALK upgrades its full-year outlook445Inside Information ALK (ALKB:DC / Nasdaq Copenhagen: ALK B) today announced that the 2026 full-year financial outlook has been upgraded reflecting a strong underlying momentum for tablet sales and...
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28.04.ALK Abello: Invitation to the presentation of ALK's first quarter 2026 results on Tuesday, 5 May 20268
20.04.ALK Abello: ALK announces successful outcome of phase 2 trial with its tablet for treatment of peanut allergy demonstrating early onset of efficacy796Inside Information The ALLIANCE phase 2 trial demonstrated proof-of-concept after only 6 months of maintenance treatment in a broad patient population comprising both children and adults.Clear dose-dependent...
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