Previous Close | 1,832.50 |
Open | 1,847.00 |
Bid | 1,865.50 x 0 |
Ask | 1,870.50 x 0 |
Day's Range | 1,840.50 - 1,871.50 |
52 Week Range | 1,823.50 - 2,205.00 |
Volume | |
Avg. Volume | 5,375,179 |
Market Cap | 3.399T |
Beta (5Y Monthly) | 0.55 |
PE Ratio (TTM) | 24.90 |
EPS (TTM) | 74.95 |
Earnings Date | Apr 25, 2023 - May 01, 2023 |
Forward Dividend & Yield | 60.00 (3.27%) |
Ex-Dividend Date | Mar 30, 2023 |
1y Target Est | 2,636.40 |
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The U.S. government will not force Pfizer Inc and Astellas Pharma Inc to lower the price of their prostate cancer drug Xtandi using its emergency "march-in" authority, the National Institutes of Health (NIH) said on Tuesday. Xtandi's wholesale cost is between $160,000-$180,000 per patient a year. Patient group the Union for Affordable Cancer Treatment first filed a petition calling on the NIH to use its authority to lower the drug's price in March 2016.
Astellas Pharma Inc. (TSE: 4503, President and CEO: Kenji Yasukawa, Ph.D., "Astellas") will present detailed results from the Phase 3 GLOW trial evaluating first-line treatment with zolbetuximab, an investigational first-in-class Claudin 18.2 (CLDN18.2) targeted monoclonal antibody, plus CAPOX (a combination chemotherapy regimen that includes capecitabine and oxaliplatin) versus placebo plus CAPOX in patients with CLDN18.2-positive, HER2-negative, locally advanced unresectable or metastatic gast
https://cdn.benzinga.com/files/images/story/2023/03/17/pfe.png?optimize=medium&dpr=2&auto=webp&crop=1200%2C800 Pfizer Inc (NYSE: PFE) and Astellas Pharma Inc (OTC: ALPMY) released topline results from the Phase 3 EMBARK trial evaluating Xtandi (enzalutamide) in non-metastatic hormone-sensitive prostate cancer. The FDA first approved Xtandi in 2012 for castration-resistant prostate cancer (CRPC), who had previously received docetaxel and was granted approval in 2014 for chemotherapy-naïve men wit