|Founded||1978 (from merger)|
Phillip Allen Sharp
|Headquarters||Cambridge, Massachusetts, U.S.|
Stelios Papadopoulos, Chairman |
George A. Scangos, CEO
|Products||Alprolix, Avonex, Eloctate, Fampyra, Gazyva*, Plegridy, Rituxan*, Tecfidera, Tysabri|
|Revenue||US$ 10.76 billion (2015) <|
|US$ 4.89 billion (2015)|
|US$ 3.55 billion (2015)|
|Total assets||US$ 19.505 billion (2015)|
|Total equity||US$ 9.37 billion (2014)|
Number of employees
|7,350 (December 2015)|
Biogen, Inc. (previously known as Biogen Idec) is an American multinational biotechnology company based in Cambridge, Massachusetts, specializing in the discovery, development, and delivery of therapies for the treatment of neurodegenerative, hematologic, and autoimmune diseases to patients worldwide.
Biogen was founded in 1978 in Geneva by several prominent biologists, including Kenneth Murray of the University of Edinburgh, Phillip Allen Sharp of the Massachusetts Institute of Technology, Walter Gilbert of Harvard (who served as CEO during the start-up phase), Heinz Schaller, University of Heidelberg and Charles Weissmann, University of Zurich (who contributed the first product interferon alpha). Gilbert and Sharp were subsequently honored with Nobel Prizes: Gilbert was recognized in 1980 with the Nobel Prize in Chemistry for his work in understanding DNA sequencing, while Sharp received the Nobel Prize in Physiology or Medicine in 1993 for his discovery of split genes.
In 2003, Biogen merged with San Diego, California-based IDEC Pharmaceuticals (formed in 1986 by biotech pioneers Ivor Royston and Howard Birndorf) and adopted the name Biogen Idec. After the merge, Biogen Idec became the 3rd largest Biotechnology company in the world. Following shifts in research core areas, the company has since shortened its name, reverting to simply Biogen. Biogen stock is a component of several stock indices such as the S&P 100, S&P 500, S&P 1500, and NASDAQ-100 and the company is listed on the NASDAQ stock exchange under the ticker symbol, BIIB.
In January 2015 the company announced it will acquire Convergence Pharmaceuticals for up to $675 million, with the acquisition aiming to accelerate the development of Convergence's pipeline, in-particular CNV1014802 – a Phase II small molecule sodium channel blocking candidate. In October 2015 the company announced it will lay off 11% of its workforce, effective immediately.
In May 2016 the company announced that it will spin off its hemophilia drug business (Eloctate and Alprolix) into a public company. In August, the company announced that the spun off company would be called Bioverativ in order to show heritage with Biogen. The company will trade on the NASDAQ exchange under the ticker symbol BIVV and will look to be spun off in early 2017.
The following is an illustration of the company's major mergers and acquisitions and historical predecessors (this is not a comprehensive list):
- George A. Scangos, Ph.D., Chief Executive Officer and Member, Board of Directors
- Susan H. Alexander, Executive Vice President, General Counsel and Corporate Secretary
- Spyros Artavanis-Tsakonas, Ph.D., Chief Scientific Officer
- Paul J. Clancy, Executive Vice President and Chief Financial Officer
- John G. Cox, Executive Vice President of Pharmaceutical Operations & Technology, interim head of Commercial Operations
- Kenneth DiPietro, Executive Vice President of Human Resources
- Adriana Karaboutis, Executive Vice President of Technology, Business Solutions & Public Affairs
- Steven H. Holtzman, Executive Vice President of Corporate Development
- Adam Koppel, M.D., Ph.D., Chief Strategy Office and Senior Vice President of Commercial Assessment and Disease Strategy
- Alfred W. Sandrock, Jr., M.D., Ph.D., Chief Medical Officer and Group Senior Vice President of Development Sciences
As is customary for a publicly traded company, Biogen is also overseen by a board of directors. The Executive Chairman and Chief Executive Officer both hold positions on the board of directors. The directors are Stelios Papadopoulos (chairman), George A. Scangos Ph.D. (CEO), Alexander J. Denner, Ph.D., Caroline Dorsa, Nancy L. Leaming, Richard C. Mulligan, Robert W. Pangia, Brian S. Posner, Eric K. Rowinsky, M.D., The Honorable Lynn Schenk, and Stephen A. Sherwin, M.D.
|Therapy||Indication (In United States unless otherwise noted)||Year Approved (US)||Year Approved (EU)||Additional Information|
|ALPROLIX™ [Coagulation Factor IX (Recombinant), Fc Fusion Protein]||Control and prevention of bleeding episodes, perioperative management and routine prophylaxis in adults and children with hemophilia B||2014||1993||Also approved in Canada and Australia.|
|AVONEX® (interferon beta-1a)||Relapsing forms of multiple sclerosis||1996||1997||Includes the AVONEX PEN auto-injector and the AVOSTARTGRIP titration kit approved in the U.S. in 2012.|
|ELOCTATE™ [Antihemophilic Factor (Recombinant), Fc Fusion Protein]||Control and prevention of bleeding episodes, perioperative (surgical) management and routine prophylaxis in adults and children with hemophilia A||2014||1999||Biogen and Swedish Orphan Biovitrum (Sobi) are collaborators in the development and commercialization of ELOCTATE.|
|FAMPYRA® (prolonged-release fampridine tablets)||Multiple sclerosis (Walking ability)||2010||2011||Marketed by Biogen in markets outside of the United States.
Commercialized in the United States as AMPYRA (dalfampridine) Extended Release Tablets, by Acorda Therapeutics.
|FUMADERM™ (fumaric acid esters)||Psoriasis German use||1994 (Germany only)||Approved in Germany.|
|GAZYVA® (obinutuzumab)||Chronic lymphocytic leukemia||2013||2014||The first medicine approved with the FDA’s Breakthrough Therapy Designation and is also currently in Phase 3 trials for NHL and diffuse large B-cell lymphoma.|
|PLEGRIDY™ (peginterferon beta-1a)||Relapsing forms of multiple sclerosis||2014||2014|
|RITUXAN® (rituximab)||Non-Hodgkin's Lymphoma (NHL)
Anti-TNF Refractory Rheumatoid Arthritis
|1997||1998 (as MabThera)||The first monoclonal antibody for cancer developed by IDEC, prior to merging with Biogen.
Currently commercialized by Roche and its subsidiary, Genentech.
|TECFIDERA® (dimethyl fumarate)||Relapsing forms of multiple sclerosis||2013||2014|
|TYSABRI® (natalizumab)||Relapsing-remitting multiple sclerosis||2004 Re-introduced in 2006||2006||Full rights purchased from partner Elan in 2013.|
Biogen has focused its R&D efforts on the discovery and development of treatments for patients with high unmet medical needs in the areas of neurology, hematology and immunology.
Investigational MS medicines:
- Daclizumab High-Yield Process (DAC HYP): is being developed as a potential once-monthly subcutaneous injection in the treatment of relapsing-remitting multiple sclerosis (RRMS). DAC HYP is being developed in collaboration with Abbvie, Inc. In June 2014, the companies announced positive top-line results from the Phase III DECIDE clinical trial, where DAC HYP demonstrated superiority over interferon beta-1a in annualized relapse rate.
- Anti-LINGO-1 (BIIB033) (Opicinumab): is the first candidate being investigated for its potential to remyelinate and repair neurons damaged by MS, currently in Phase 2 trials.
Biogen has several candidates in Phase 1 and 2 clinical trials in neurodegenerative and immunological diseases including MS, Alzheimer’s disease, neuropathic pain, spinal muscular atrophy and lupus nephritis:
- Phase 2a: anti-LINGO-1 molecule (Opicinumab) in acute optic neuritis
- Phase 2b: anti-TWEAK monoclonal antibody in lupus nephritis
- Phase 2a: STX-100 in patients with idiopathic pulmonary fibrosis
- Phase 2: Neublastin for neuropathic pain in 2013
- Phase 3: Nusinersen (ISIS-SMNRx) for spinal muscular atrophy in infants and children, in collaboration with Ionis Pharmaceuticals
- Phase 3: BIIB037 (Aducanumab), Biogen’s first clinical study in Alzheimer’s disease
- Phase 1/2: BIIB067 (ISIS-SOD1Rx) for Amyotrophic Lateral Sclerosis (ALS), in collaboration with Ionis
In February 2012, Biogen formalized a joint venture with Samsung, creating Samsung Bioepis. This joint venture brings Biogen’s expertise and capabilities in protein engineering, cell line development, and recombinant biologics manufacturing to position the joint venture so Biogen can participate in the emerging market for biosimilars.
In early 2014, Biogen entered into an agreement with Eisai, Inc., to jointly develop and commercialize two of their candidates for Alzheimer’s disease, which have the potential to reduce Aβ plaques that form in the brains of patients, as well as to slow the formation of new plaques, potentially improving symptoms and suppressing disease progression.
- Achievement of carbon neutrality, a milestone reached through a multi-year initiative to reduce its own emissions and by investing in environmental projects to offset the remaining carbon associated with its business, including emissions from suppliers and employee commuting and business travel.
- No. 1 on the Newsweek list of “Top Green Companies in the World 2015."
- Named the biotechnology industry leader on the Dow Jones Sustainability Index World in 2014 and 2015.
- Named the most sustainable company in the world on the Global 100 list.
- More than $1 billion in financial assistance to patients in the form of free drug, drug copay assistance, infusion assistance, and charitable contributions.
- A joint commitment with Swedish Orphan Biovitrum AB (Sobi) to donate up to 1 billion international units (IUs) of clotting factor therapy over the next 10 years to humanitarian aid programs in the developing world to help individuals with hemophilia.
- Investment of $7 million worldwide by the Biogen Foundation to expand the company’s global commitment to science, technology, engineering and mathematics (STEM) education.
- Creation of the “Underserved Populations Initiative” to help improve MS outcomes among racial and ethnic minority populations in the United States.
- Achievement of a perfect score of 100 on the Human Rights Campaign’s Corporate Equality Index.
- Creation of a program to sponsor high-potential women leaders to take on roles on corporate boards in the life sciences and other industries.
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