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Impact News +++ BICO Group AB GAAP EPS of -SEK 0.53, revenue of SEK 336.1M (SeekingAlpha) +++ BICO Aktie +5,10%

LUNDBECK A Aktie

 >LUNDBECK A Aktienkurs 
5.54 EUR    +12.3%    (TradegateBSX)
Ask: 5.55 EUR / 1800 Stück
Bid: 5.53 EUR / 1810 Stück
Tagesumsatz: 34110 Stück
Realtime Kurs von 7:30 bis 22 Uhr!
LUNDBECK A Aktie über LYNX handeln
>LUNDBECK A Performance
1 Woche: +5,1%
1 Monat: +1,5%
3 Monate: +5,3%
6 Monate: +1,3%
1 Jahr: +16,2%
laufendes Jahr: +2,5%
>LUNDBECK A Aktie
Name:  H. LUNDBECK A/S SER.A DK1
Land:  Dänemark
Sektor:  Gesundheit
ISIN/ Wkn:  DK0061804697 / A3DMBU
Symbol/ Ticker:  LDBB (Frankfurt)
Kürzel:  FRA:LDBB, ETR:LDBB, LDBB:GR
Index:  -
Profil:  H. Lundbeck A/S, commonly known as Lundbeck, is a Danish international pharmaceutical company specializing in the research, development, manufacturing, marketing, and sale of innovative therapies for brain diseases. Its portfolio targets disorders su..
>Volltext..
Marktkapitalisierung:  4489.58 Mio. EUR
Unternehmenswert:  5682.73 Mio. EUR
Umsatz:  3341.38 Mio. EUR
EBITDA:  1239.79 Mio. EUR
Nettogewinn:  492.88 Mio. EUR
Gewinn je Aktie:  0.5 EUR
Schulden:  1456.51 Mio. EUR
Liquide Mittel:  260.7 Mio. EUR
Operativer Cashflow:  648.42 Mio. EUR
Bargeldquote:  0.22
Umsatzwachstum:  8.31%
Gewinnwachstum:  12.04%
Dividende je Aktie:  0.15 EUR
Dividendenrendite:  3.19%
Dividendenschätzung:  3.21%
Div. Historie:  19.03.26 - 0.15388493€
27.03.25 - 0.12712899€
>weitere anzeigen...
Insiderhandel -
Suchwörter:  LUNDBECK A, LUNDBECK
Letzte Datenerhebung:  19.08.26
>LUNDBECK A Kennzahlen
Aktien/ Unternehmen:
Aktien: 199.02 Mio. St.
Frei handelbar: 19.92%
Leerverk. Aktien: -
Rückkaufquote: 0.06%
Mitarbeiter: 5214
Umsatz/Mitarb.: 0.63 Mio. EUR
Analysten:
Analystenrating: No rating
Kursziel: -
Bewertung:
KGV: 9.56
KGV lG: -
KUV: 1.42
KBV: 1.38
PEG-Ratio: 0.77
EV/EBITDA: 4.58
Rentabilität:
Bruttomarge: 79.09%
Gewinnmarge: 14.75%
Operative Marge: 27.75%
Managementeffizenz:
Gesamtkaprendite: 6.94%
Eigenkaprendite: 14.73%
 >LUNDBECK A Anleihen 
>LUNDBECK A Peer Group
Gesundheit, Parkinson- Behandlung, Neurologische Erkrankungen/ Schlaganfälle, Psychische Erkrankungen/ Depressionen/ Schizophrenie, Demenz/ Alzheimer- Behandlung
 
19.08.26 - 08:42
Lundbeck profit rises as Vyepti growth offsets higher costs (Investing.com)
 
Um den gesamten Artikel unter investing.com zu lesen, klicken Sie bitte auf die Überschrift...
19.08.26 - 08:06
Strong growth from Vyepti® and focused commercial execution drive total revenue growth of +16% CER (+13% CER underlying) in H1 2026 (PR Newswire)
 
VALBY, Denmark, Aug. 19, 2026 /PRNewswire/ -- Key highlights Lundbeck'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. and Europe delivering double-digit growth. The performance reflected continued strong commercial......
19.08.26 - 08:03
Strong growth from Vyepti® and focused commercial execution drive total revenue growth of +16% CER (+13% CER underlying) in H1 2026 (PR Newswire)
 
VALBY, Denmark, Aug. 19, 2026 /PRNewswire/ -- Key highlights Lundbeck'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. and Europe delivering double-digit growth. The performance reflected continued strong commercial......
19.08.26 - 07:42
Lundbeckfond Invest A/S launches voluntary exchange offer for A-shares in H. Lundbeck A/S (PR Newswire)
 
VALBY, 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 and major shareholder in Lundbeck, has today launched a voluntary exchange offer to eligible......
24.07.26 - 12:00
FDA grants fast track designation for Lundbeck′s Lu AH69593 (PBR)
 
Lu AH69593 is an oral, small-molecule agonist of the orexin 2 receptor (OX2R). The compound is currently being studied in a Phase Ib clinical trial focused on patients The post FDA grants fast track designation for Lundbeck's Lu AH69593 appeared first on Pharmaceutical Business review....
23.07.26 - 09:36
Lundbeck receives FDA Fast Track designation for Lu AH69593, an investigational orexin 2 receptor agonist for narcolepsy (PR Newswire)
 
The 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 is critically located in the main biological pathway involved in wakefulness and sleep-wake regulation Lu AH69593 is......
20.07.26 - 09:51
Lundbeck announces last patient randomized in DEEp OCEAN, a large Phase III trial in developmental and epileptic encephalopathies (DEEs) (PR Newswire)
 
DEEp 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 Broadest pivotal trial to date, enrolling patients with a wide range of DEE syndromes, the majority......
24.06.26 - 12:03
Tarek Samad appointed EVP, Head of Research & Development at Lundbeck (PR Newswire)
 
VALBY, Denmark, June 24, 2026 /PRNewswire/ -- H. Lundbeck A/S (Lundbeck) today announced that Tarek Samad has been appointed Executive Vice President and Head of Research & Development (R&D) and will join the Executive Leadership Team (ELT) effective 1 September 2026. Tarek Samad succeeds......
24.06.26 - 11:30
Tarek Samad appointed EVP, Head of Research & Development at Lundbeck (Cision)
 
Valby, Denmark, 24 June, 2026 – H. Lundbeck A/S (Lundbeck) today announced that Tarek Samad has been appointed Executive Vice President and Head of Research & Development (R&D) and will join the Executive Leadership Team (ELT) effective 1 September 2026. Tarek Samad succeeds Johan Luthman, who has informed the Board of Directors and ELT of his decision to retire after seven years with Lundbeck. A transition period will commence in July 2026 to ensure a seamless handover of responsibilities, and Johan Luthman will remain with Lundbeck until the end of 2026 to ensure continuity across...
24.06.26 - 09:54
Lundbeck presents new Vyepti® (eptinezumab) and bocunebart migraine portfolio data at EAN 2026 (PR Newswire)
 
Five migraine presentations will showcase Lundbeck's current and future approaches to migraine prevention, including new data for eptinezumab and Phase IIb PROCEED primary data for the investigational treatment, bocunebart Eptinezumab data explore patient-centered outcomes in chronic......
15.06.26 - 08:06
Lundbeck presents new Phase II asedebart data in Cushing′s disease at ENDO 2026 (PR Newswire)
 
Asedebart is an investigational monoclonal antibody designed to neutralize excess adrenocorticotropic hormone (ACTH) and reduce downstream cortisol production in Cushing's disease (CD) Urinary free cortisol (UFC) normalization is a clinically relevant measure in CD, where chronic cortisol......
14.06.26 - 22:30
Lundbeck reports early success for experimental Cushing′s disease treatment (SeekingAlpha)
 
Um den gesamten Artikel unter seekingalpha.com zu lesen, klicken Sie bitte auf die Überschrift...
10.06.26 - 08:24
Lundbeck to present new patient data on neuroendocrine and neuroimmunology programs at ENDO 2026 (PR Newswire)
 
Upcoming presentations at ENDO 2026 highlight Lundbeck's Focused Innovator strategy and continued expansion into rare neuroendocrine diseases with high unmet medical needs The scientific program showcases Lundbeck's investigational neurohormonal and neuroimmunological targeted therapeutic......
09.06.26 - 21:27
Neuraptive Therapeutics, Inc. gibt wichtige organisatorische Neuerungen bekannt, um die Fortschritte des Unternehmens auf dem Weg zur Markteinführung zu unterstützen (Business Wire)
 
Ulf Wiinberg in den Verwaltungsrat berufen William „Bill“ MacKenzie zum Senior Vice President – Finance ernannt CHESTERBROOK, Pa.--(BUSINESS WIRE)--Neuraptive Therapeutics gab heute die Ernennung von Ulf Wiinberg in den Verwaltungsrat sowie von William „Bill“ MacKenzie zum Senior Vice President – Finance bekannt. Herr Wiinberg ist eine erfahrene Führungskraft in den Bereichen Biotechnologie, Pharmazie und Gesundheitswesen mit einer langjährigen internationalen Karriere. Als Mitglied des Verwaltungsrats wird er mit strategischer Beratung und Branchenexpertise dazu beitragen, die Entwicklungs- und Vermarktungsstrategie des Unternehmens zu unterstützen. Zu Herrn Wiinbergs beruflichen Stationen zählt die Tätigkeit als CEO der X-Vax Technology, Inc. von 2017 bis 2024; davor war er von 2008 bis 2014 CEO von Lundbeck. Von 2002 bis 2008 war er Mitglied des Führungsgremiums von Wyeth; in dieser Zeit war er von 2002 bis 2005 weltweiter Präsident von Wyeth Consumer Healthcare und bis 2008, als Wye...
08.06.26 - 15:06
Neuraptive Therapeutics, Inc. Announces Key Organizational Updates to Support the Company′s Advancement Toward Commercialization (Business Wire)
 
Ulf Wiinberg appointed to Board of Directors William “Bill” MacKenzie hired as Senior Vice President – Finance CHESTERBROOK, Pa.--(BUSINESS WIRE)--Neuraptive Therapeutics today announced the appointment of Ulf Wiinberg to its Board of Directors and William “Bill” MacKenzie as Senior Vice President – Finance. Mr. Wiinberg is a seasoned biotechnology, pharmaceutical and healthcare industries executive with an extensive global career. As a member of the Board of Directors, he will contribute strategic guidance and industry expertise to support the Company's development and commercialization strategy. Mr. Wiinberg's experience includes serving as CEO of X-Vax Technology, Inc. from 2017 until 2024 and prior to that, he was CEO of Lundbeck from 2008 until 2014. From 2002 to 2008, he was a member of Wyeth's Management Committee and during this time, he was Worldwide President of Wyeth Consumer Healthcare from 2002 to 2005, and President of Europe/Middle East/Africa until 2008, when Wyeth was acqui...
04.06.26 - 23:09
Lundbeck presents positive Phase IIb data for bocunebart (Lu AG09222; anti-PACAP mAb) in migraine prevention at the AHS congress (PR Newswire)
 
The intravenous part of the Phase IIb clinical dose-finding trial PROCEED met its primary endpoint, with bocunebart demonstrating a statistically significant reduction in monthly migraine days versus placebo over Weeks 1–12 in patients with one to four prior preventive treatment failures......
04.06.26 - 14:06
Lundbeck Presents New VYEPTI® (eptinezumab-jjmr) and Bocunebart Migraine Data at the American Headache Society 68th Annual Scientific Meeting (Business Wire)
 
New 12-month data from the INFUSE study show patient-reported outcomes related to multiple migraine-related cognitive symptoms in participants who failed at least one prior calcitonin gene-related peptide (CGRP)-targeted therapy1 Six-month data from the INFUSE study was recently published in Cephalalgia Reports, an official journal of the International Headache Society New PROCEED phase 2b route of administration and dose-finding trial results of bocunebart (Lu AG09222; anti-PACAP mAb) being investigated in migraine prevention2 DEERFIELD, Ill.--(BUSINESS WIRE)--Lundbeck US, the US subsidiaries of H. Lundbeck A/S., today announced the presentation of new VYEPTI® (eptinezumab-jjmr) data at the American Headache Society's (AHS) 68th Annual Scientific Meeting, taking place June 4-7, 2026, in Orlando, Florida. The presentations will share findings from the INFUSE, DELIVER, SUNSET, and RESOLUTION trials, featuring real-world data and phase 3 clinical trial post-hoc analyses of VYEPTI and patient-reported outc...
03.06.26 - 14:01
Lundbeck Partners with Cradle to Discover and Optimize Brain Disorder Treatments (Cision)
 
Collaboration's initial focus will focus on two antibody programs targeting CNS diseases VALBY, Denmark & AMSTERDAM, 03 June 2026 – H. Lundbeck A/S (Lundbeck), a global biopharmaceutical company focused exclusively on brain health, and Cradle, a leading AI platform for protein engineering, today announced a partnership to help Lundbeck discover and optimize biotherapeutics that ultimately can improve patient outcomes. It is estimated that more than half of the world's population is impacted by brain disorders, and the effects are felt throughout society. Speeding up innovation time to...
26.05.26 - 08:30
Lundbeck receives marketing authorization for Vyepti® (eptinezumab) in South Korea for the preventive treatment of migraine (PR Newswire)
 
Approval granted by South Korea's Ministry of Food and Drug Safety (MFDS) Eptinezumab is an anti-calcitonin gene-related peptide (CGRP) monoclonal antibody for the preventive treatment of migraine in adults Authorization supported by the Phase 3 SUNRISE trial conducted in a predominantly......
18.05.26 - 10:51
Lundbeck receives orphan drug designation in Japan for asedebart for the treatment of patients with congenital adrenal hyperplasia and Cushing′s disease (PR Newswire)
 
Congenital adrenal hyperplasia (CAH) and Cushing's disease (CD) are rare disorders characterized by excess adrenocorticotropic hormone (ACTH) produced in the brain1,2 Current treatments are limited by suboptimal disease control and treatment-related complications3,4 Asedebart (Lu AG13909)......
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