Previous Close | 84.06 |
Open | 84.15 |
Bid | 82.12 x N/A |
Ask | 86.33 x N/A |
Day's Range | 83.65 - 84.74 |
52 Week Range | 73.79 - 94.77 |
Volume | |
Avg. Volume | 964,190 |
Market Cap | 193.116B |
Beta (5Y Monthly) | 0.49 |
PE Ratio (TTM) | 26.24 |
EPS (TTM) | N/A |
Earnings Date | N/A |
Forward Dividend & Yield | 3.20 (3.78%) |
Ex-Dividend Date | Mar 09, 2023 |
1y Target Est | N/A |
With 5.6 months of additional follow-up and 78.3% of patients having completed Kisqali® (ribociclib) investigational treatment, the updated analysis shows sustained iDFS benefit and stability in secondary endpoints including overall survival (OS)1,2 iDFS benefit remains consistent across key patient subgroups; among patients with stage II and stage III tumors, Kisqali lowered risk by 30% and 24.5%, respectively1,2 Latest analysis continues to show a well-tolerated safety profile in line with pre
Novartis today announced that the U.S. Food and Drug Administration (FDA) approved Fabhalta® (iptacopan) as the first oral monotherapy for the treatment of adults with paroxysmal nocturnal hemoglobinuria (PNH)1. Fabhalta is a Factor B inhibitor that acts proximally in the alternative complement pathway of the immune system, providing comprehensive control of red blood cell (RBC) destruction within and outside the blood vessels (intra- and extravascular hemolysis [IVH and EVH]). In clinical trial
Ad hoc announcement pursuant to Art. 53 LR ‘Pure-play’ innovative medicines strategy focused on four therapeutic areas and five technology platforms, which offer potential for consistent growth Mid-term sales guidance upgrade to 5% CAGR (2022-27), with core operating income margin of ~40%+ by 2027, driven by continued strong momentum of key growth drivers Confidence to grow mid-single digit longer-term based on the foundational strength of de-risked existing brands and pipeline assets Focused st