Onyx Pharmaceuticals

Last updated

Onyx Pharmaceuticals Incorporated
Company type Subsidiary
Industry Biotechnology
Founded1992
Headquarters South San Francisco California United States
Key people
N. Anthony (Tony) Coles (CEO)
Products Sorafenib (Nexavar)
Number of employees
500
Parent Amgen
Website www.amgen.com

Onyx Pharmaceuticals Inc. has been a biopharmaceutical company headquartered in South San Francisco, California. The company developed and marketed medicines for the treatment of cancer. Onyx was founded in 1992 by Kevin J. Kinsella and Frank McCormick Ph.D., FRS. [1] McCormick served as the chief scientific officer until 1998, [1] while Kinsella was the firm's chairman. [2] In 2009, the company acquired Proteolix, Inc., a private biotechnology company, for $276 million in cash plus additional milestone payments. [3] [ better source needed ] In January 2012, the company was named "the top biotechnology takeover target in 2012" through an industry survey. [4] Onyx president and chief executive officer (CEO) N. Anthony Coles had said that Onyx liked its prospects as an independent company and was focused on bringing new therapies to patients. [5] However, at the end of August 2013, Amgen announced it was acquiring Onyx in an agreed $10.4 billion deal. [6]

Contents

Initial funding for the formation of Onyx came from biotechnology firm Chiron Corporation (granted a 43% stake in the new company) and venture capital investors: Avalon Ventures, Institutional Venture Partners, J. H. Whitney & Company, and Kleiner Perkins Caufield & Byers. [2] McCormick had been working on cancer treatments at Chiron before he was selected as vice president of research at the newly formed company, leading the company's research program. [2] The acting president of the firm at its inception was Samuel D. Colella, a partner at Institutional Venture Partners (an original Onyx backer). [2]

Products and development

Sorafenib, co-developed and co-marketed with Bayer and sold under the trade name Nexavar, is a drug approved in the United States for the treatment of advanced renal cell carcinoma (kidney cancer) in 2005, and for the treatment of inoperable hepatocellular carcinoma, the most common form of liver cancer, in 2007. [7] [8] Sorafenib has also been evaluated in other types of cancer, including those of the thyroid (as a treatment of last resort) and breast (in comparison to capecitabine). [9] [10]

Carfilzomib (marketed under the trade name Kyprolis) was approved by the FDA on June 20, 2012, for use in patients with multiple myeloma who have received at least two prior therapies, including treatment with bortezomib and an immunomodulatory therapy, and have demonstrated disease progression on or within 60 days of completion of the last therapy. [11] [12] Carfilzomib is also being evaluated in other stages of multiple myeloma. The most commonly reported adverse reactions (incidence ≥ 30%) are fatigue, anemia, nausea, thrombocytopenia, dyspnea, diarrhea, and pyrexia. [12]

Regorafenib (marketed under the trade name Stivarga), is currently being studied as a potential treatment option in multiple tumor types. [13] On 27 September 2012, the FDA approved regorafenib for the treatment of patients with metastatic colorectal cancer (CRC) who have been previously treated with fluoropyrimidine-, oxaliplatin, and irinotecan-based chemotherapy, an anti-VEGF therapy, and, if KRAS wild-type, an anti-EGFR therapy. [14] On February 25, 2013, the FDA approved regorafenib in a second indication to treat patients with locally advanced, unresectable or metastatic gastrointestinal stromal tumor (GIST) who have been previously treated with imatinib mesylate and sunitinib malate. [15] Regorafenib is a compound developed by Bayer. The most common adverse reactions (>/=20%) are asthenia/fatigue, HFSR, diarrhea, decreased appetite/food intake, hypertension, mucositis, dysphonia, and infection, pain (not otherwise specified), decreased weight, gastrointestinal and abdominal pain, rash, fever, and nausea. [16] In 2011, Bayer entered into an agreement with Onyx under which Onyx will receive a 20 percent royalty on any future global net sales of regorafenib in oncology. Bayer and Onyx jointly promote Stivarga in the United States. [17]

In June 2013, Amgen Inc offered to buy the shares of Onyx Pharmaceuticals for $120 per share, sending the shares up by around 30% after the news was announced. [18] Onyx announced on June 30, 2013, that it rejected the unsolicited proposal from Amgen. The Onyx board has authorized its financial adviser to contact potential suitors. [19] The acquisition was formally announced on 25 August 2013. [6]

    In July 2014 the company announced the phase III failure of a Sorafenib-Capecitabine combination trial. The drug combination failed to increase progression free survival of patients with advanced breast cancer. [20]

    Related Research Articles

    <span class="mw-page-title-main">Amgen</span> American multinational biopharmaceutical company

    Amgen Inc. is an American multinational biopharmaceutical company headquartered in Thousand Oaks, California. One of the world's largest independent biotechnology companies, As of 2022, Amgen has approximately 24,000 staff in total.

    <span class="mw-page-title-main">Sorafenib</span> Chemical compound

    Sorafenib, sold under the brand name Nexavar, is a kinase inhibitor drug approved for the treatment of primary kidney cancer, advanced primary liver cancer, FLT3-ITD positive AML and radioactive iodine resistant advanced thyroid carcinoma.

    <span class="mw-page-title-main">Lapatinib</span> Cancer medication

    Lapatinib (INN), used in the form of lapatinib ditosylate (USAN) is an orally active drug for breast cancer and other solid tumours. It is a dual tyrosine kinase inhibitor which interrupts the HER2/neu and epidermal growth factor receptor (EGFR) pathways. It is used in combination therapy for HER2-positive breast cancer. It is used for the treatment of patients with advanced or metastatic breast cancer whose tumors overexpress HER2 (ErbB2).

    Panitumumab, sold under the brand name Vectibix, is a fully human monoclonal antibody specific to the epidermal growth factor receptor.

    Proteolix, Inc., was a private biotechnology company with headquarters in South San Francisco, California. Proteolix was founded in 2003 based on technology developed by co-founders Craig M. Crews and Raymond J. Deshaies. Susan Molineaux and Phil Whitcomeref>"Paid Notice: Deaths WHITCOME, DR. PHILIP J."The New York Times. 2005-12-18. ISSN 0362-4331. Retrieved 2024-06-19.</ref> joined as co-founders.

    Ramucirumab is a fully human monoclonal antibody (IgG1) developed for the treatment of solid tumors. This drug was developed by ImClone Systems Inc. It was isolated from a native phage display library from Dyax.

    Regorafenib, sold under the brand name Stivarga among others, is an oral multi-kinase inhibitor developed by Bayer which targets angiogenic, stromal and oncogenic receptor tyrosine kinase (RTK). Regorafenib shows anti-angiogenic activity due to its dual targeted VEGFR2-TIE2 tyrosine kinase inhibition. Since 2009 it was studied as a potential treatment option in multiple tumor types. By 2015 it had two US approvals for advanced cancers.

    <span class="mw-page-title-main">Genta (company)</span> Biotechnology company

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    <span class="mw-page-title-main">Tivozanib</span> Medication

    Tivozanib, sold under the brand name Fotivda, is a medication used for the treatment of advanced renal cell carcinoma. It is an oral VEGF receptor tyrosine kinase inhibitor.

    <span class="mw-page-title-main">Carfilzomib</span> Chemical compound

    Carfilzomib, sold under the brand name Kyprolis, is an anti-cancer medication acting as a selective proteasome inhibitor. Chemically, it is a tetrapeptide epoxyketone and an analog of epoxomicin. It was developed by Onyx Pharmaceuticals.

    <span class="mw-page-title-main">Trastuzumab emtansine</span> Pharmaceutical drug

    Trastuzumab emtansine, sold under the brand name Kadcyla, is an antibody-drug conjugate consisting of the humanized monoclonal antibody trastuzumab (Herceptin) covalently linked to the cytotoxic agent DM1. Trastuzumab alone stops growth of cancer cells by binding to the HER2 receptor, whereas trastuzumab emtansine undergoes receptor-mediated internalization into cells, is catabolized in lysosomes where DM1-containing catabolites are released and subsequently bind tubulin to cause mitotic arrest and cell death. Trastuzumab binding to HER2 prevents homodimerization or heterodimerization (HER2/HER3) of the receptor, ultimately inhibiting the activation of MAPK and PI3K/AKT cellular signalling pathways. Because the monoclonal antibody targets HER2, and HER2 is only over-expressed in cancer cells, the conjugate delivers the cytotoxic agent DM1 specifically to tumor cells. The conjugate is abbreviated T-DM1.

    <span class="mw-page-title-main">Daratumumab</span> Monoclonal antibody

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    <span class="mw-page-title-main">Isatuximab</span> Monoclonal antibody

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    <span class="mw-page-title-main">Oprozomib</span> Chemical compound

    Oprozomib is an orally active second-generation proteasome inhibitor developed by Proteolix, which was acquired by Onyx Pharmaceuticals, an Amgen subsidiary, in 2009. It selectively inhibits chymotrypsin-like activity of both the constitutive proteasome (PSMB5) and immunoproteasome (LMP7).

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    <span class="mw-page-title-main">Tucatinib</span> Chemical compound

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    <span class="mw-page-title-main">Sotorasib</span> Chemical compound

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    <span class="mw-page-title-main">Avapritinib</span> Chemical compound

    Avapritinib, sold under the brand name Ayvakit among others, is a medication used for the treatment of advanced systemic mastocytosis and for the treatment of tumors due to one specific rare mutation: it is specifically intended for adults with unresectable or metastatic gastrointestinal stromal tumor (GIST) that harbor a platelet-derived growth factor receptor alpha (PDGFRA) exon 18 mutation. Avapritinib is a kinase inhibitor.

    References

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    17. "Securities and Exchange Commission 8K Form". Securities and Exchange Commission. Retrieved July 29, 2013.
    18. Caroline Humer (June 28, 2013). "U.S. biotech Amgen offered to buy Onyx for $120 per share: report". Reuters.
    19. "Onyx confirms, rejects Amgen's $120-per-share bid". Yahoo! Finance. Retrieved June 30, 2013.
    20. "Sorafenib-Capecitabine Combination Fails Phase III Trial". July 25, 2014.