Seagen Inc. (formerly Seattle Genetics, Inc.) is an American biotechnology company focused on developing and commercializing innovative, empowered monoclonal antibody-based therapies for the treatment of cancer. The company, headquartered in Bothell, Washington (a suburb of Seattle), was considered the industry leader in antibody-drug conjugates or ADCs, a technology designed to harness the targeting ability of monoclonal antibodies to deliver cell-killing agents directly to cancer cells, with its development of drugs such as Adcetris, Padcev, and Tivdak. Antibody-drug conjugates are intended to spare non-targeted cells and thus reduce many of the toxic effects of traditional chemotherapy, while potentially enhancing antitumor activity. The company's flagship product Adcetris (brentuximab vedotin) is commercially available for four indications in more than 65 countries, including the U.S., Canada, Japan and members of the European Union. To expand on the clinical opportunities of brentuximab vedotin, Seattle Genetics is conducting a broad clinical development program to evaluate its therapeutic potential in earlier lines of its approved indications as well as in a range of other lymphoma and non-lymphoma settings. The company is jointly developing brentuximab vedotin in collaboration with Takeda Pharmaceutical Company. Under the terms of the collaboration, Seattle Genetics has full commercialization rights to brentuximab vedotin in the United States and Canada. Takeda has exclusive rights to commercialize the product candidate in all other countries. In addition to brentuximab vedotin, Seattle Genetics' product pipeline includes enfortumab vedotin, being co-developed with Astellas Pharma, tisotumab vedotin, being co-developed with Genmab, SGN-LIV1A, an ADC targeting LIV-1, and several immuno-oncology agents in phase 1 studies. In January 2018, the company announced it would acquire Cascadian Therapeutics for $614 million. In September 2020, Merck & Co announced it would purchase $1 billion of Seagen's common stock, with both companies co-developing lead treatment: ladiratuzumab vedotin. In November 2022, the company announced the appointment of David R. Epstein as Chief Executive Officer and Director. Pfizer agreed to acquire Seagen in March 2023 at an enterprise value of $43 billion.
Collaboration agreements Seattle Genetics has collaboration agreements with Takeda Oncology Company (formerly Millennium) to develop and commercialize brentuximab vedotin. The company also has collaboration agreements for their ADC technology with a number of biotechnology and pharmaceutical companies, including AbbVie, Bayer Celldex Therapeutics, Inc., Daiichi Sankyo, Genentech, Inc., GlaxoSmithKline, Pfizer, Inc., and PSMA Development Company LLC, as well as ADC co-development agreements with Agensys, Inc., an affiliate of Astellas Pharma, and Oxford BioTherapeutics Ltd.
Technology
MMAE-based
Seattle Genetics' proprietary monomethyl auristatin E or MMAE-based antibody-drug conjugate technology, employed in brentuximab vedotin, empowers monoclonal antibodies to treat cancer. Brentuximab vedotin, for example, links the chimeric anti-CD30 monoclonal antibody (cAC10) via a protease-cleavable linker to MMAE. This ADC employs a linker system that is designed to be stable in the bloodstream but to release MMAE upon internalization into CD30-expressing tumor cells. This approach is intended to spare non-targeted (healthy) cells and thus reduce many of the toxic effects of traditional chemotherapy while potentially enhancing antitumor activity. (See also vedotins)
History
Early years Seattle Genetics was founded in 1997, by Henry Perry Fell, Jr. and Clay Siegall, and is headquartered in Bothell, Washington, a suburb of Seattle. The company completed an initial public offering in March 2001, and prior to its acquisition by Pfizer, it was traded on the Nasdaq Stock Market under the symbol SGEN, and was a component of the Nasdaq-100. As of December 2016, the company has more than 900 employees throughout the United States.
2009 19 February: pivotal trial for brentuximab vedotin for Hodgkin lymphoma 18 June: Phase II trial of brentuximab vedotin for anaplastic large cell lymphoma 24 July: initiation of re-treatment clinical trial of brentuximab vedotin 10 August: milestone achievement in collaboration with MedImmune through initiation of Phase I clinical trial of MEDI-547. 8 September: milestone achievement in collaboration with Bayer for the submission of investigational new drug application with the FDA 5 October: discontinuation of Phase IIb trial with dazcetuzumab (also known as SGN-40 or huS2C6) for the treatment of diffuse large B-cell lymphoma 16 November: initiation of Phase I clinical trial for SGN-75 (INN: vorsetuzumab mafodotin) 11 December: termination of collaboration with Genentech for SGN-40 21 December: announcement of new collaboration with GlaxoSmithKline ($12 million up front payment, up to $390 million in milestone payments) In 2009, when it appeared that ADCETRIS could reach the market, the company realized that commercial skills would need to be grown in-house and/or acquired. This led to a decision to grow a commercial team to address the United States and Canadian markets, and a marketing collaboration with Takeda to cover the rest of the world. By 2018, however, the company was confident it could conduct a global commercialization venture.
2010 2 February: initiation of phase I combination clinical trial of brentuximab vedotin (SGN-35) for Hodgkin lymphoma 3 March: milestone achievement under collaboration with Genentech 8 April: initiation of Phase III trial for brentuximab vedotin (SGN-35) for post transplant Hodgkin lymphoma 20 April: $9.5 million payment from Genentech to extend collaboration 20 July: initiation of Phase I clinical trial of ASG-5ME for treatment of pancreatic cancer 3 August: expansion of collaboration with Genentech ($12 million upfront payment, up to $900 million in potential fees and milestone payments) 2 September: milestone achievement in collaboration with Agensys for initiation of Phase I trial of AGS-16M8F 14 September: entry into collaboration with Genmab 20 October: initiation of Phase I clinical trial of ASG-5ME in prostate cancer treatment
… excerpt ends here. Continue reading the full article.
