Previous Close | 93.08 |
Open | 92.85 |
Bid | 0.00 x 900 |
Ask | 0.00 x 800 |
Day's Range | 92.35 - 92.93 |
52 Week Range | 92.19 - 108.78 |
Volume | |
Avg. Volume | 1,498,658 |
Market Cap | 189.694B |
Beta (5Y Monthly) | 0.47 |
PE Ratio (TTM) | 22.58 |
EPS (TTM) | N/A |
Earnings Date | N/A |
Forward Dividend & Yield | 3.78 (4.08%) |
Ex-Dividend Date | Mar 07, 2024 |
1y Target Est | N/A |
Continuous Kesimpta® treatment for up to six years showed sustained efficacy in recently diagnosed (≤3 years) treatment-naïve people living with relapsing multiple sclerosis (RMS) in an analysis of the ALITHIOS open-label extension study1Similar efficacy outcomes were demonstrated in a separate analysis of continuous Kesimpta treatment for up to six years in the overall ALITHIOS study population2 Switch from teriflunomide to Kesimpta resulted in significant improvements across several efficacy o
APPLAUSE-IgAN is first and only Phase III study to demonstrate significant proteinuria reduction by targeting the complement system in patients with IgAN1IgAN is a heterogeneous, progressive, rare kidney disease and is a major cause of chronic kidney disease worldwide2; complement activation is a key driver of glomerular inflammation in IgAN3,4There is a need for effective, targeted therapies for IgAN2,5; up to 30% of patients with persistent proteinuria (≥1 g/day) may progress to kidney failure
– Arvinas to receive a $150 million upfront payment for the license of ARV-766 and the sale of Arvinas’ preclinical AR-V7 program, with the potential under the License Agreement for up to $1.01 billion in development, regulatory, and commercial milestones, as well as tiered royalties – – Novartis to be responsible for worldwide clinical development and commercialization of ARV-766 – – Partnership expected to accelerate and broaden the development of ARV-766 as a potential first-in-class treatmen