Entries by arcticnovartis

Novartis Entresto® US patent upheld by US Court of Appeals

Novartis Entresto® US patent upheld by US Court of Appeals
arcticnovartis
Mon, 01/13/2025 – 07:19

Read more about Novartis Entresto® US patent upheld by US Court of Appeals

Basel, January 13, 2025 – Novartis is pleased with the dec…

Novartis intrathecal onasemnogene abeparvovec Phase III study meets primary endpoint in children and young adults with SMA

Novartis intrathecal onasemnogene abeparvovec Phase III study meets primary endpoint in children and young adults with SMA
arcticnovartis
Mon, 12/30/2024 – 06:49

Read more about Novartis intrathecal onasemnogene abeparvovec Phase III study meets p…

Longer-term Novartis Kisqali® NATALEE data show durable reduction in distant recurrence in broad population of patients with early breast cancer

Longer-term Novartis Kisqali® NATALEE data show durable reduction in distant recurrence in broad population of patients with early breast cancer
arcticnovartis
Tue, 12/10/2024 – 15:04

Read more about Longer-term Novartis Kisqali® NATALEE data show…

Longer-term data for Novartis Scemblix® reinforce superior efficacy with favorable safety and tolerability profile in adults with newly diagnosed CML

Longer-term data for Novartis Scemblix® reinforce superior efficacy with favorable safety and tolerability profile in adults with newly diagnosed CML
arcticnovartis
Sun, 12/08/2024 – 18:34

Read more about Longer-term data for Novartis Scemblix® re…

New Phase IIIB data shows Novartis Fabhalta® improved hemoglobin levels in adult patients with paroxysmal nocturnal hemoglobinuria who switched from anti-C5 therapy

New Phase IIIB data shows Novartis Fabhalta® improved hemoglobin levels in adult patients with paroxysmal nocturnal hemoglobinuria who switched from anti-C5 therapy
arcticnovartis
Fri, 12/06/2024 – 07:19

Read more about New Phase IIIB data shows …

Novartis Kisqali® receives European Commission approval in a broad population of patients with HR+/HER2- early breast cancer at high risk of recurrence

Novartis Kisqali® receives European Commission approval in a broad population of patients with HR+/HER2- early breast cancer at high risk of recurrence
arcticnovartis
Wed, 11/27/2024 – 07:19

Read more about Novartis Kisqali® receives European Comm…

Novartis highlights new 96-week results from Phase III Scemblix® ASC4FIRST trial at ASH and late-breaking analysis from Phase III Kisqali® NATALEE trial at SABCS

Novartis highlights new 96-week results from Phase III Scemblix® ASC4FIRST trial at ASH and late-breaking analysis from Phase III Kisqali® NATALEE trial at SABCS
arcticnovartis
Mon, 11/25/2024 – 07:19

Read more about Novartis highlights new 96-wee…

Novartis upgrades mid-term guidance and highlights deep pipeline in core therapeutic areas to drive long-term growth

Novartis upgrades mid-term guidance and highlights deep pipeline in core therapeutic areas to drive long-term growth
arcticnovartis
Thu, 11/21/2024 – 07:04

Read more about Novartis upgrades mid-term guidance and highlights deep pipeline in core th…

Novartis ranks first in 2024 Access to Medicine Index

Novartis ranks first in 2024 Access to Medicine Index
arcticnovartis
Tue, 11/19/2024 – 14:04

Read more about Novartis ranks first in 2024 Access to Medicine Index

The Index spotlights Novartis leadership in research and development…

Novartis Scemblix® FDA approved in newly diagnosed CML, offering superior efficacy, and favorable safety and tolerability profile

Novartis Scemblix® FDA approved in newly diagnosed CML, offering superior efficacy, and favorable safety and tolerability profile
arcticnovartis
Tue, 10/29/2024 – 20:14

Read more about Novartis Scemblix® FDA approved in newly diagnosed CML, offeri…