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HL

WKN: A3DMBU | ISIN: DK0061804697 | Ticker-Symbol: LDBB
Tradegate
18.09.26 | 16:48
5,400 Euro
-0,37 % -0,020
Branche
Pharma
Aktienmarkt
Sonstige
1-Jahres-Chart
H LUNDBECK A/S A Chart 1 Jahr
5-Tage-Chart
H LUNDBECK A/S A 5-Tage-Chart
RealtimeGeldBriefZeit
5,4005,45018.09.
5,4005,43018.09.

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DoH. LUNDBECK A/S: Transactions with shares and linked securities in Lundbeck made by executives and their closely associated parties1
H LUNDBECK A/S A Aktie jetzt für 0€ handeln
MiH. Lundbeck A/S: Lundbeck receives marketing authorization for Vyepti (eptinezumab) in Japan for the prevention of migraine attacks351Approval granted by Japan's Ministry of Health, Labour and Welfare (MHLW)Eptinezumab is the only intravenous (IV) CGRP-targeted preventive treatment approved for the prevention of migraine attacks...
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DiDeutsche Bank stuft Lundbeck ab: Sorgen um Blockbuster-Medikament Rexulti7
DiH. Lundbeck A/S: Lundbeck announces last patient randomized in DEEp SEA, a Phase III trial of bexicaserin in Dravet syndrome362DEEp SEA is a global Phase III trial evaluating efficacy, safety and tolerability of the investigational molecule bexicaserin in children and adults with Dravet syndrome1Completion of randomization...
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11.09.H. Lundbeck A/S: The U.S. FDA grants orphan drug designation for Lundbeck's investigational anti-ACTH monoclonal antibody asedebart for treatment of endogenous Cushing's syndrome472The U.S. FDA has granted Orphan Drug Designation for asedebart (Lu AG13909), Lundbeck's novel investigational anti-ACTH monoclonal antibody, for the treatment...
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03.09.H. Lundbeck A/S: Lundbeck to highlight mechanistic insights on bexicaserin's dual mode of action at the European Epilepsy Congress370Preclinical data provide mechanistic insight into bexicaserin's dual mode of action, increasing inhibitory while decreasing excitatory neuronal activity, suggesting a broader antiseizure...
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25.08.Lundbeck, Eversana Expand AI Commercialization Partnership2
25.08.Lundbeck taps EVERSANA's AI Agency for commercialisation-
25.08.Lundbeck's asedebart receives EC orphan designation in Cushing's syndrome1
24.08.H. LUNDBECK A/S: European Commission grants orphan designation for Lundbeck's investigational anti-ACTH monoclonal antibody asedebart for Cushing's syndrome of endogenous origin5
21.08.Lundbeck continues neuroscience evolution as CEO keeps company 'punching above its weight'5
19.08.Lundbeck H1 2026 slides: Vyepti drives 16% revenue growth1
19.08.Earnings Call: H. Lundbeck erzielt starkes Wachstum im ersten Halbjahr 2026 dank Vyepti3
19.08.H. Lundbeck A/S: Strong growth from Vyepti and focused commercial execution drive total revenue growth of +16% CER (+13% CER underlying) in H1 2026623VALBY, Denmark, Aug. 19, 2026 /PRNewswire/ -- Key highlightsLundbeck's total revenue grew by +16% CER[1] (+11% DKK) to DKK 13,588 million in the first six months of 2026, with the U.S....
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19.08.H. Lundbeck A/S: Lundbeckfond Invest A/S launches voluntary exchange offer for A-shares in H. Lundbeck A/S561VALBY, Denmark, Aug. 19, 2026 /PRNewswire/ -- H. Lundbeck A/S ("Lundbeck") hereby informs that Lundbeckfond Invest A/S ("Lundbeckfond Invest"), a fully owned subsidiary of the Lundbeck Foundation...
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19.08.H. Lundbeck A/S Reveals Advance In Q2 Bottom Line3
24.07.FDA grants fast track designation for Lundbeck's Lu AH695937
23.07.H. Lundbeck A/S: Lundbeck receives FDA Fast Track designation for Lu AH69593, an investigational orexin 2 receptor agonist for narcolepsy462The U.S. FDA has granted Fast Track designation to Lu AH69593, an oral orexin 2 receptor agonist, for the treatment of patients with narcolepsy The orexin 2 receptor...
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20.07.Lundbeck preps for key bexicaserin data around year-end1
20.07.H. Lundbeck A/S: Lundbeck announces last patient randomized in DEEp OCEAN, a large Phase III trial in developmental and epileptic encephalopathies (DEEs)637DEEp OCEAN is a global trial designed to evaluate the investigational molecule bexicaserin for the treatment of seizures associated with DEEs, a diverse group of childhood-onset epilepsies1...
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