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17/09 Transactions with shares and linked securities in Lundbeck made by executives and their closely associated parties
16/09 H. Lundbeck A/S Receives Marketing Authorization for Vyepti (Eptinezumab) in Japan for Prevention of Migraine Attacks
16/09 H. Lundbeck's Vyepti Wins Marketing Regulatory Nod in Japan
16/09 Lundbeck receives marketing authorization for Vyepti® (eptinezumab) in Japan for the prevention of migraine attacks
15/09 H. Lundbeck A/S Completes Randomization In DEEp SEA Phase III Trial Of Bexicaserin In Dravet Syndrome
15/09 Lundbeck announces last patient randomized in DEEp SEA, a Phase III trial of bexicaserin in Dravet syndrome
11/09 Lundbeck's Asedebart Gets US FDA Orphan Drug Designation for Endogenous Cushing's Syndrome
11/09 The U.S. FDA grants orphan drug designation for Lundbeck's investigational anti-ACTH monoclonal antibody asedebart for treatment of endogenous Cushing's syndrome
03/09 H. Lundbeck A/S Highlights Mechanistic Insights and Clinical Data on Bexicaserin At the European Epilepsy Congress
03/09 Lundbeck to highlight mechanistic insights on bexicaserin's dual mode of action at the European Epilepsy Congress
24/08 Lundbeck's Obtains Orphan Designation in EU for Investigational Treatment for Cushing's Syndrome
24/08 European Commission grants orphan designation for Lundbeck's investigational anti-ACTH monoclonal antibody asedebart for Cushing's syndrome of endogenous origin
20/08 Cancer vaccines finally garner the spotlight
19/08 H Lundbeck : Q2 beat, but pipeline execution remains non-negotiable
19/08 Danish Pharma H. Lundbeck Expects No Slowdown for Primary Growth Driver Brands
19/08 H. Lundbeck A/S Reports Earnings Results for the Second Quarter and Six Months Ended June 30, 2026
19/08 H. Lundbeck's Major Shareholder Kicks Off Voluntary Share Exchange Offer
19/08 Lundbeckfond Invest A/S launches voluntary exchange offer for A-shares in H. Lundbeck A/S
19/08 Strong growth from Vyepti[®] and focused commercial execution drive total revenue growth of +16% CER (+13% CER underlying) in H1 2026
19/08 H. Lundbeck A/S Maintains Earnings Guidance for the Year 2026
11/08 Moberg Pharma Appoints Business, Medical Chiefs
23/07 Lundbeck Receives FDA Fast Track Designation for Lu AH69593, Investigational Orexin 2 Receptor Agonist for Narcolepsy
23/07 Lundbeck Secures US FDA Fast Track Designation for Narcolepsy Drug
23/07 Lundbeck receives FDA Fast Track designation for Lu AH69593, an investigational orexin 2 receptor agonist for narcolepsy
20/07 H. Lundbeck A/S Completes Randomization In DEEp OCEAN Phase III Clinical Trial Evaluating Bexicaserin For Treatment Of Seizures Associated With Developmental And Epileptic Encephalopathies
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