
IgAN is a progressive, rare kidney disease in which the immune system attacks the kidneys, often causing glomerular inflammation and…
The results from the Phase III STEER study add to the clinical data and emerging real-world evidence for the use…
Following recent data announcements at ESMO 20246, Novartis will continue to evaluate NATALEE patients for longer-term outcomes, including overall survival,…
The company remains on track to deliver core operating income margin of 40%+ by 2027, benefiting from continued strong sales…
According to Novartis, the positive CHMP decision is based on robust data from the Phase III NATALEE trial.
Novartis plans to present results from this trial at an upcoming medical meeting and share them with regulatory agencies including…
Atrasentan has the potential to help transform how IgAN is managed for many people living with this complex illness, the…
Novartis continues to progress the workstreams for implementation of both a delisting of MorphoSys and a domination and profit and…
The study reported a safety profile consistent with the adult population studied in NETTER-1, the pivotal trial for approval of…
Multiple Sclerosis is a disease in which the immune system damages the protective covering of nerves. In this condition, nerve…
Novartis will be presenting further data from the renal portfolio at future medical meetings, it added.
Under the agreement, Novartis has acquired global rights to develop and commercialize the drug, ARV-766, for an upfront payment of…
Of late, however, there have been several instances of MNCs quitting India or scaling down their stake in their India…
Pelabresib is also being studied in patients with essential thrombocythemia (ET), which is currently in Phase 2 in second line…
Data were presented at the 2024 American Society of Clinical Oncology (ASCO) Gastrointestinal (GI) Cancers Symposium.
Vontobel pharmaceuticals analyst Stefan Schneider said a deal made sense for Novartis, with Cytokinetics active in the cardiovascular field, one…
Details will be presented at an upcoming medical conference and included as part of regulatory submissions in 2024
Up to 88 percent of patients on anti-C5 treatment may have persistent anemia with over one-third of those patients requiring…