Novartis employs creative deal structure to establish Borealis Biosciences – divests legacy Chinook site, invests to form new company and engages in R&D collaboration
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Novartis receives FDA accelerated approval for Fabhalta® (iptacopan), the first and only complement inhibitor for the reduction of proteinuria in primary IgA nephropathy (IgAN)
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Ad hoc announcement pursuant to Art. 53 LR
Novartis Scemblix® granted FDA Priority Review for the treatment of adults with newly diagnosed CML
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- Priority Review based on ASC4FIRST Phase III study with Scemblix® data first to show significantly improved molecular response and a favorable safety and tolerability profile compared to standard of care therapies (imatinib and 2G TKIs)1
- Treatment options combining high efficacy with safety and tolerability represent a critical gap in care for long-term CML management1
Novartis erzielt im zweiten Quartal weiterhin kräftige Umsatzsteigerungen und erhöht die Kerngewinnmarge; Gewinnprognose für das Geschäftsjahr 2024 angehoben
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Ad-hoc-Mitteilung gemäss Art. 53 KR
Novartis a poursuivi au T2 la forte croissance de son chiffre d’affaires et l’expansion de sa marge core; hausse des prévisions de son résultat opérationnel core pour 2024
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Annonce événementielle au sens de l’art. 53 RC
Résultats du deuxième trimestre (T2)
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