US09062X1037 - Common Stock
NASDAQ:BIIB (2/6/2023, 10:28:04 AM)+4.63 (+1.63%)
GICS Sector | Health Care | ||
GICS Industry | Biotechnology |
Valuation | Growth | ||
Profitability | Health | ||
Dividend |
Earnings (Last) | 02-01 2023-02-01/amc | Earnings (Next) | 05-01 2023-05-01/amc |
Ins Owners | 0.2% | Inst Owners | 84.8% |
Market Cap | 41.51B | Shares | 144.00M |
PE | 16.2 | Fwd PE | 18.04 |
Dividend Yield | N/A | Analysts | 77.5 |
IPO | 09-17 1991-09-17 |
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Biogen, Inc. is a biopharmaceutical company, which engages in discovering, developing, and delivering therapies for neurological and neurodegenerative diseases. The company is headquartered in Cambridge, Massachusetts and currently employs 9,610 full-time employees. The company is focused on discovering, developing and delivering therapies for people living with serious neurological and neurodegenerative diseases as well as related therapeutic adjacencies. The company has a portfolio of medicines to treat multiple sclerosis (MS), spinal muscular atrophy (SMA) and Alzheimer's disease. Its marketed products include TECFIDERA, VUMERITY, AVONEX, PLEGRIDY, TYSABRI and FAMPYRA for the treatment of MS; SPINRAZA for the treatment of SMA; ADUHELM for the treatment of Alzheimer's disease; and FUMADERM for the treatment of severe plaque psoriasis. The company also has a collaboration agreement with Genentech, Inc. (Genentech), a member of the Roche Group, with respect to RITUXAN for the treatment of non-Hodgkin's lymphoma, chronic lymphocytic leukemia (CLL) and other conditions; RITUXAN HYCELA for the treatment of non-Hodgkin's lymphoma and CLL; GAZYVA; OCREVUS; and other potential anti-CD20 therapies, including mosunetuzumab.
BIOGEN INC
225 Binney Street
Cambridge MASSACHUSETTS 02142
P: 17814642000.0
CEO: Michel Vounatsos
Employees: 9610
Website: https://www.biogen.com/
Biogen (BIIB) and Sage Therapeutics (SAGE) said Monday that FDA accepted the marketing application for oral depression therapy zuranolone under priority review. Read the full story here.
Eisai Co.’s sales of the Alzheimer’s drug Leqembi in the US are “ahead of expectations” despite the steps required to administer it, said Ivan Cheung, the company’s global Alzheimer’s disease officer.
Zuranolone is being evaluated as a potential 14-day, rapid-acting, once-daily, oral medication to treat major depressive disorder (MDD) and postpartum...
The company that remains still has a large pipeline of non-migraine assets.
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