Entries by arcticnovartis

Novartis setzt die starke Dynamik fort mit zweistelligem Umsatzwachstum, robusten Margensteigerungen und mehreren Zulassungen im ersten Quartal

Novartis setzt die starke Dynamik fort mit zweistelligem Umsatzwachstum, robusten Margensteigerungen und mehreren Zulassungen im ersten Quartal
arcticnovartis
Tue, 04/29/2025 – 07:03

Read more about Novartis setzt die starke Dynamik fort mit zweis…

Novartis continues strong momentum with double-digit sales growth, robust margin expansion and multiple approvals in Q1  

Novartis continues strong momentum with double-digit sales growth, robust margin expansion and multiple approvals in Q1  
arcticnovartis
Tue, 04/29/2025 – 07:03

Read more about Novartis continues strong momentum with double-digit sales g…

Novartis receives FDA accelerated approval for Vanrafia® (atrasentan), the first and only selective endothelin A receptor antagonist for proteinuria reduction in primary IgA nephropathy (IgAN)

Novartis receives FDA accelerated approval for Vanrafia® (atrasentan), the first and only selective endothelin A receptor antagonist for proteinuria reduction in primary IgA nephropathy (IgAN)
arcticnovartis
Thu, 04/03/2025 – 02:19

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Novartis appoints Karen Hale, Chief Legal and Compliance Officer, as Klaus Moosmayer, Chief Ethics, Risk & Compliance Officer, steps down from the Executive Committee of Novartis

Novartis appoints Karen Hale, Chief Legal and Compliance Officer, as Klaus Moosmayer, Chief Ethics, Risk & Compliance Officer, steps down from the Executive Committee of Novartis
arcticnovartis
Mon, 03/31/2025 – 07:04

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FDA approves Novartis radioligand therapy Pluvicto® for earlier use before chemotherapy in PSMA-positive metastatic castration-resistant prostate cancer

FDA approves Novartis radioligand therapy Pluvicto® for earlier use before chemotherapy in PSMA-positive metastatic castration-resistant prostate cancer
arcticnovartis
Fri, 03/28/2025 – 17:58

Read more about FDA approves Novartis radioligand thera…

Novartis to present new data at AAN, including seven-year disability outcomes and safety analysis of Kesimpta® in people with relapsing multiple sclerosis

Novartis to present new data at AAN, including seven-year disability outcomes and safety analysis of Kesimpta® in people with relapsing multiple sclerosis
arcticnovartis
Tue, 03/25/2025 – 07:18

Read more about Novartis to present new data at AAN, …

Novartis receives third FDA approval for oral Fabhalta® (iptacopan) – the first and only treatment approved in C3 glomerulopathy (C3G)

Novartis receives third FDA approval for oral Fabhalta® (iptacopan) – the first and only treatment approved in C3 glomerulopathy (C3G)
arcticnovartis
Fri, 03/21/2025 – 00:19

Read more about Novartis receives third FDA approval for oral Fabhalta® (…

New Novartis Phase III data demonstrate meaningful efficacy and safety results of intrathecal onasemnogene abeparvovec in broad patient population with SMA

New Novartis Phase III data demonstrate meaningful efficacy and safety results of intrathecal onasemnogene abeparvovec in broad patient population with SMA
arcticnovartis
Wed, 03/19/2025 – 14:04

Read more about New Novartis Phase III data demonstr…

Novartis shareholders approve all resolutions proposed by the Board of Directors at the 2025 Annual General Meeting

Novartis shareholders approve all resolutions proposed by the Board of Directors at the 2025 Annual General Meeting
arcticnovartis
Fri, 03/07/2025 – 15:19

Read more about Novartis shareholders approve all resolutions proposed by the Board of Direc…

Aktionäre von Novartis heissen an der Generalversammlung 2025 alle Anträge des Verwaltungsrats gut

Aktionäre von Novartis heissen an der Generalversammlung 2025 alle Anträge des Verwaltungsrats gut
arcticnovartis
Fri, 03/07/2025 – 15:19

Read more about Aktionäre von Novartis heissen an der Generalversammlung 2025 alle Anträge des Verwaltungsrat…