|Wholly owned subsidiary of Roche|
|Headquarters||South San Francisco, California, United States|
|Ian T. Clark, CEO
Sandra J. Horning, M.D.
Michael D. Varney, Ph.D.
Frederick C. Kentz, III, Legal
Timothy L. Moore
Nancy Vitale, HR
Severin Schwan, Chairman of Genentech Board of Directors, CEO of Roche Group
|Products||Avastin, Herceptin, Rituxan, Perjeta, Kadcyla, Gazyva, Tarceva, Esbriet, Cotellic, Alecensa, Zelboraf, Nutropin, ACTEMRA, Lucentis, Xolair, Activase, Xeloda, Boniva, Cathflo Activase, TNKase, CellCept, Pegasys, Pulmozyme, Tamiflu, Valcyte, Anaprox, Cytovene, EC-Naprosyn, Erivedge, Fuzeon, Invirase, Klonopin, Kytril, Naprosyn, Rocephin, Roferon-A, Romazicon, Valium, Xenical, Zenapax|
Number of employees
|13,720 (August 21, 2015)|
|Slogan||Doing now what patients need next (previously "In business for life")|
The company was founded in 1976 by venture capitalist Robert A. Swanson and biochemist Herbert Boyer. Boyer is considered to be a pioneer in the field of recombinant DNA technology. In 1973, Boyer and his colleague Stanley Norman Cohen demonstrated that restriction enzymes could be used as "scissors" to cut DNA fragments of interest from one source, to be ligated into a similarly cut plasmid vector. While Cohen returned to the laboratory in academia, Swanson contacted Boyer to found the company. Boyer worked with Arthur Riggs and Keiichi Itakura from the Beckman Research Institute, and the group became the first to successfully express a human gene in bacteria when they produced the hormone somatostatin in 1977. David Goeddel and Dennis Kleid were then added to the group, and contributed to its success with synthetic human insulin in 1978.
Genentech markets itself as a research-driven corporation that follows the science to make innovations. It employs more than 1,100 researchers, scientists and postdocs and covers a wide range of scientific activity—from molecular biology to protein chemistry to bioinformatics and physiology. Genentech scientists in these various areas of expertise currently focus their efforts on five disease categories: Oncology, Immunology, Tissue Growth and Repair, Neuroscience and Infectious Disease. Genentech's recent hiring and acquisitions indicate an intent to expand into microbiology and medical Imaging.
In December 2006, Genentech sold its Porriño, Spain facility to Lonza and acquired an exclusive right to purchase Lonza's mammalian cell culture manufacturing facility under construction in Singapore. In June 2007, Genentech began the construction and development of an E. coli manufacturing facility, also in Singapore, for the worldwide production of Lucentis (ranibizumab injection) bulk drug substance.
Genentech Inc Political Action Committee
Genentech Inc Political Action Committee is a U.S. Federal Political Action Committee (PAC), created to "aggregate contributions from members or employees and their families to donate to candidates for federal office."
In 1999, Genentech agreed to pay the University of California, San Francisco $200 million to settle a nine-year-old patent dispute. In 1990, UCSF sued Genentech for $400 million in compensation for alleged theft of technology developed at the university and covered by a 1982 patent. Genentech claimed that they developed Protropin (recombinant somatotropin/human growth hormone), independently of UCSF. A jury ruled that the university's patent was valid last July[year needed], but wasn't able to decide whether Protropin was based upon UCSF research or not. Protropin, a drug used to treat dwarfism, was Genentech's first marketed drug and its $2 billion in sales has contributed greatly to its position as an industry leader. The settlement was to be divided as follows: $30 million to the University of California General Fund, $85 million to the three inventors and two collaborating scientists, $50 million towards a new teaching and research campus for UCSF, and $35 million to support university-wide research.
In 2009, The New York Times reported that Genentech's talking points on health care reform appeared verbatim in the official statements of several Members of Congress during the national health care reform debate.
- 1982 - Synthetic "human" insulin approved by the U.S. Food and Drug Administration (FDA), thanks largely to its partnership with insulin manufacturer Eli Lilly and Company, who shepherded the product through the FDA approval process. The product (Humulin) was licensed to and manufactured by Lilly, and was the first-ever approved genetically engineered human therapeutic.
- 1985 - Protropin (somatrem) - Supplementary growth hormone for children with growth hormone deficiency (ceased manufacturing 2004).
- 1987 - Activase (alteplase) - A recombinant tissue plasminogen activator (tPa) used to dissolve blood clots in patients with acute myocardial infarction. Also used to treat non-hemorrhagic stroke.
- 1990 - Actimmune (interferon gamma 1b) - Treatment of chronic granulomatous disease (licensed to Intermune).
- 1993 - Nutropin (recombinant somatropin) - Growth hormone for children and adults for treatment before kidney transplant due to chronic renal insufficiency.
- 1993 - Pulmozyme (dornase alfa) - Inhalation treatment for children and young adults with cystic fibrosis - recombinant DNAse.
- 1997 - Rituxan (rituximab) - Treatment for specific kinds of non-Hodgkins lymphomas. In 2006, also approved for rheumatoid arthritis.
- 1998 - Herceptin (trastuzumab) - Treatment for metastatic breast cancer patients with tumors that overexpress the HER2 gene. Recently approved for adjuvant therapy for breast cancer. FDA also recently approved Trastuzumab for metastatic gastric cancer with HER2 receptor site positive.
- 2000 - TNKase (tenecteplase) - "Clot-busting" drug to treat acute myocardial infarction.
- 2003 - Xolair (omalizumab) - Subcutaneous injection for moderate to severe persistent asthma.
- 2003 - Raptiva (efalizumab) - Antibody designed to block the activation and reactivation of T cells that lead to the development of psoriasis. Developed in partnership with XOMA. In 2009, voluntary U.S. market withdrawal after reports of progressive multifocal leukoencephalopathy.
- 2004 - Avastin (bevacizumab) - Anti-VEGF monoclonal antibody for the treatment of metastatic cancer of the colon or rectum. In 2006, also approved for locally advanced, recurrent or metastatic non-small cell lung cancer. In 2008, accelerated approval was granted for Avastin in combination with chemotherapy for previously untreated advanced HER2-negative breast cancer. In 2009, Avastin gained its fifth approval for treatment of glioblastoma multiforme, and sixth approval for the treatment of metastatic renal cell carcinoma. It was most publicized for its approval in advanced breast cancer treatment, but the FDA approval for breast cancer treatment was subsequently revoked in November, 2011.
- 2004 - Tarceva (erlotinib) - Treatment for patients with locally advanced or metastatic non-small cell lung cancer, and pancreatic cancer.
- 2006 - Lucentis (ranibizumab injection) - Treatment of neovascular (wet) age-related macular degeneration (AMD). The FDA approved LUCENTIS after a Priority Review (six-month). Genentech started shipping product on June 30, 2006, the day the product was approved.
- 2010 - Actemra (tocilizumab) - The first interleukin-6 (IL-6) receptor-inhibiting monoclonal antibody approved to treat rheumatoid arthritis (RA).
- 2011 - Zelboraf (vemurafenib) - For the treatment of a type of skin cancer called melanoma that has spread to other parts of the body or cannot be removed by surgery, and has a certain type of abnormal BRAF gene.
- 2012 - Erivedge (vismodegib) - Treatment for advanced basal-cell carcinoma (BCC). A small molecule inhibitor that targets a key protein in the Hedgehog signaling pathway. This is the first approved therapy for advanced BCC.
- 2012 - Perjeta (pertuzumab) - For use in combination with Herceptin (trastuzumab) and docetaxel chemotherapy for the treatment of patients with previously untreated HER2-positive metastatic breast cancer.
- 2013 - Kadcyla (ado-trastuzumab emtansine) - The first Genentech antibody-drug conjugate (ADC) to receive FDA approval. It consists of trastuzumab (Herceptin) linked to a cytotoxic agent mertansine (DM1), used in the treatment of HER2-positive metastatic breast cancer.
- 2013 - Gazyva (obinutuzumab) - For use in combination with chlorambucil to treat patients with previously untreated chronic lymphocytic leukemia (CLL). Gazyva is the first drug with breakthrough therapy designation to receive FDA approval.
- 2014 - Esbriet (pirfenidone) - An anti-fibrotic drug for the treatment of idiopathic pulmonary fibrosis (IPF). Developed by Intermune, Inc.
- 2015 - Cotellic (cobimetinib) - For use in combination with ZELBORAF (vemurafenib), to treat a type of skin cancer called melanoma that has spread to other parts of the body or cannot be removed by surgery, and that has a certain type of abnormal “BRAF” gene.
- 2015 - Alecensa (alectinib) - Treatment for non-small cell lung cancer (NSCLC).
- Ongoing Work - Genentech is working on DR6 blocking and anti-N-APP monoclonal antibodies as a potential treatment to delay progression of neuronal destruction in early Alzheimer's disease. To the extent that prevention of neuronal destruction via DR-6 and N-APP would require ongoing intervention, the effective half-life of any monoclonal antibody treatment would have to be substantial. An siRNA approach against DR-6, or vaccine against N-APP may circumvent these limitations.
Awards and recognitions
- Fortune Magazine named Genentech number one on its 2006 list of the "100 Best Companies To Work For." This was the first number one ranking for the company, which has now been on the list for 18 consecutive years. In 2007, it dropped to second place, behind Google. The company ranked 5th in 2008, 7th in 2009, 19th in 2010, 35th in 2011, 68th in 2012, 36th in 2013, 6th in 2014, 9th in 2015, and 11th in 2016. The ranking is based on anonymous employee responses to a survey as well as an evaluation of the company's policies and culture.
- Genentech was named one of the 100 Best Companies for Working Mothers in 2004, 2006-8 and 2010-11 by Working Mother Magazine.
- It was named as one of the 100 best corporate citizens 2006 by the Business Ethics Magazine. The company participates in various policy and civic leadership groups, such as TechNet, and sponsors independent third-party research and publications, such as the journal Nature.
- Genentech was named Top Employer by Science Magazine on October 7, 2010, where it has been recognized for nine consecutive years.
- In March 2008, Genentech was named Most Admired Pharmaceutical Company by Fortune for the second consecutive year.
- In July 2010, Genentech was named on the "Top 100 Best Places to Work in IT" list by ComputerWorld magazine.
- In December 2008, Glassdoor.com rated the Genentech CEO Arthur D. Levinson as the "nicest" CEO of 2008 with a 93% approval rating.
- Genentech was featured in the documentary film Something Ventured which premiered in 2011.
- The Economist rated Genentech as the Most Innovative Corporation of 2013.
- "About Us". Gene.com. Retrieved 22 Aug 2014.
- "Genentech - Great Place to Work Reviews". Retrieved 2016-05-10.
- Staff writers (2014-07-02). "Genentech acquires Seragon". Genetic Engineering & Biotechnology News. Retrieved 2014-07-02.
- Russo, E. (2003). "Special Report: The birth of biotechnology". Nature. 421 (6921): 456–457. doi:10.1038/nj6921-456a. PMID 12540923.
- "Genentech was founded by venture capitalist Robert A. Swanson and biochemist Dr. Herbert W. Boyer. After a meeting in 1976, the two decided to start a biotechnology company, Genentech. Although the two confidently assert that it was the first biotech company, others clearly came before, including Cetus Corporation which was founded in 1971." Genentech. "Corporate Overview".
- Cohen, S.; Chang, A.; Boyer, H.; Helling, R. (1973). "Construction of biologically functional bacterial plasmids in vitro". Proceedings of the National Academy of Sciences of the United States of America. 70 (11): 3240–3244. doi:10.1073/pnas.70.11.3240. PMC . PMID 4594039.
- "In January 1976, 28-year-old venture capitalist Robert Swanson entered the picture. A successful cold-call to Boyer's lab led to a couple of beers—and an agreement to start a pharmaceutical company. Investing $500 each, they capitalized a new business, Genentech, to seek practical uses for Boyer and Cohen's engineered proteins. Swanson raised money for staff and labs...""Who made America? Herbert Boyer". PBS.
- Itakura, K.; Hirose, T.; Crea, R.; Riggs, A. D.; Heyneker, H. L.; Bolivar, F.; Boyer, H. W. (1977). "Expression in Escherichia coli of a chemically synthesized gene for the hormone somatostatin". Science. 198 (4321): 1056–1063. doi:10.1126/science.412251. PMID 412251.
- Morse, Andrew (2006-05-10). "Chugai Shares Post Healthy Gain On Prospects for Cancer Drug". The Wall Street Journal. Retrieved 2008-09-26.
- Staff writers (2008-07-21). "Roche Makes $43.7B Bid for Genentech". Genetic Engineering & Biotechnology News. ISSN 1935-472X. Retrieved 2008-09-26.
- Genentech Inc Political Action Committee, Bloomberg Business, nd, retrieved 17 July 2015
- Genentech Press Release. "University of California and Genentech Settle Patent Infringement Lawsuits". Genentech Inc. Retrieved 16 November 2015.
- Pear, Robert. "In House, Many Spoke with One Voice: Lobbyists", New York Times, 15 November 2009.
- "Working Mother Magazine".
- "Science Magazine".
- "No. 58: Genentech Inc.". ComputerWorld Magazine. Archived from the original on 16 January 2009.
- "Glassdoor.com Lists Naughtiest and Nicest C.E.O.'s of 2008". The New York Times. December 26, 2008. Retrieved May 3, 2010.
- "Innovation Awards: And the winners are...". The Economist. November 30, 2013.
- Sally Smith Hughes. Genentech: The Beginnings of Biotech (University of Chicago Press; 2011).
- GenenLab Notebook: "Biotech's Beginnings" - New Genentech Employee Booklet (1996)
- * "Prescription for Profits: How the Pharmaceutical Industry Bankrolled the Unholy Marriage Between Science and Business" by Linda Marsa, Scribner (1997)
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