Seagen

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Seagen Inc.
Formerly called
Seattle Genetics, Inc.
(1997–2020)
Public
Traded as
Industry Biotechnology, pharmaceutical
Founded 1997; 27 years ago (1997)
Headquarters Bothell, Washington, U.S.
Key people
Products Brentuximab vedotin and other antibody-drug conjugates
Revenue Increase 2.176 Billion(2020)[2]
Number of employees
2700 (2021)
Website seagen.com

Seagen 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), is 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. 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)[3] 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[4] 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.[5]

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.[6]

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.[7]

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)

Company history

Early years

Seattle Genetics was founded in 1997, by Henry Perry Fell, Jr.[8] and Clay Siegall,[1] and is headquartered in Bothell, Washington, a suburb of Seattle. The company completed an initial public offering in March 2001, and is traded on the Nasdaq Stock Market under the symbol SGEN. As of December 2016, the company has more than 900 employees throughout the United States.[9][10]

2009

19 February: pivotal trial for brentuximab vedotin for Hodgkin lymphoma[11]
18 June: Phase II trial of brentuximab vedotin for anaplastic large cell lymphoma[12]
24 July: initiation of re-treatment clinical trial of brentuximab vedotin[13]
10 August: milestone achievement in collaboration with MedImmune through initiation of Phase I clinical trial of MEDI-547.[14][15]
8 September: milestone achievement in collaboration with Bayer for the submission of investigational new drug application with the FDA[16]
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[17]
16 November: initiation of Phase I clinical trial for SGN-75 (INN: vorsetuzumab mafodotin)[18]
11 December: termination of collaboration with Genentech for SGN-40[19]
21 December: announcement of new collaboration with GlaxoSmithKline ($12 million up front payment, up to $390 million in milestone payments)[20]

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.[1] 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.[1] By 2018, however, the company was confident it could conduct a global commercialization venture.[1]

2010

2 February: initiation of phase I combination clinical trial of brentuximab vedotin (SGN-35) for Hodgkin Lymphoma[21]
3 March: milestone achievement under collaboration with Genentech[22]
8 April: initiation of Phase III trial for brentuximab vedotin (SGN-35) for post transplant Hodgkin Lymphoma[23]
20 April: $9.5 million payment from Genentech to extend collaboration[24]
20 July: initiation of Phase I clinical trial of ASG-5ME for treatment of pancreatic cancer[25]
3 August: expansion of collaboration with Genentech ($12 million upfront payment, up to $900 million in potential fees and milestone payments)[26]
2 September: milestone achievement in collaboration with Agensys for initiation of Phase I trial of AGS-16M8F[27][28]
14 September: entry into collaboration with Genmab[29]
20 October: initiation of Phase I clinical trial of ASG-5ME in prostate cancer treatment[30]

2011

6 January: entry into collaboration with Pfizer ($8 million upfront payment, $200+ million in potential milestone payments)[31]
1 March: initiation of Phase I clinical trial of brentuximab vedotin for use in conjunction with chemotherapy for treatment of systemic anaplastic large cell lymphoma[32]
15 March: expansion of collaboration with the Millennium Pharmaceuticals (Takeda Oncology)[33]
22 March: announcement of collaboration with Abbott ($8 million upfront payment, plus potential royalties and milestone payments)[34]
11 April: James Fan, SG manager of clinical programming, commits suicide one day after being indicted for insider trading in Seattle Genetics securities[35][36]
19 April: expansion of collaboration with Genmab[37]
19 August accelerated FDA approval for brentuximab vedotin for use in treatment of Hodgkin lymphoma and systemic anaplastic large cell lymphoma (ALCL)[38]
23 August: initiation of Phase II trial of ADCETRIS in CD30-positive non-Hodgkin lymphoma[39]
9 September: collaboration with Oxford BioTherapeutics[40]
25 October: initiation of Phase II clinical trial of ADCETRIS in CD30-positive non-lymphoma malignancies[41]

2012

4 June: interim Phase I data from ASG-5ME in prostate cancer[42]
5 July: initiation of global Phase III trial of ADCETRIS against CD30-expressing cutaneous T-cell lymphoma[43]
24 August: initiation of Phase Ib trial of SGN-75 (INN: vorsetuzumab mafodotin) for use in combination with everolimus in patients with renal cell carcinoma[44]
9 October: milestone achievement under collaboration with Genentech by advancements of two antibody conjugates into Phase II trials[45]
17 October: initiation of Phase II trial of ADCETRIS in age 60+ Hodgkin lymphoma patients[46]
23 October: expansion of collaboration with Abbott (upfront payment of $25 million, milestone payment up to $220 million)[47]
1 November: initiation of global Phase III trial of ADCETRIS in untreated advanced Hodgkin lymphoma patients[48]
26 November: received orphan drug designation for ADCETRIS treatment of mycosis fungoides[49]

2013

1 February: Health Canada approves ADCETRIS for treatment of relapsed refractory Hodgkin lymphoma[50]
6 February: initiation of two Phase I trials of SGN-CD19A[51]
25 June: new collaboration with Bayer[52]
15 July: initiation of Phase I trial of SGN-CD33A in treatment of acute myeloid leukemia (AML)[53]
15 August: initiation of Phase II trial of ADCETRIS for diffuse large B-cell lymphoma[54][55]
21 October: initiation of Phase I trial of SGN-LIV1A for patients with LIV-1-positive metastatic breast cancer[56][57]

2014

29 September: brentuximab vedotin was successfully used as a consolidation therapy in a late-stage trial for patients with a type of lymphatic cancer.[58]
8 December: Data of Brentuximab Vedotin in Diffuse Large B-cell Lymphoma presented at the Annual Meeting of the American Society of Hematology ref>Seattle Genetics Presents ADCETRIS® (Brentuximab Vedotin) Data in Diffuse Large B-cell Lymphoma at ASH Annual Meeting Reuters</ref>

2015

12 January: clinical collaboration with Bristol-Myers Squibb to evaluate combination of brentuximab vedotin and nivolumab in hematologic malignancies[59]
18 February: Supplemental Biologics License Application (BLA) for Brentuximab Vedotin in Post-Transplant Hodgkin Lymphoma Patients at High Risk of Relapse[60]
8 June: collaboration with Unum Therapeutics to develop and commercialise its new antibody-coupled T-cell receptor (ACTR) therapies for cancer, generating up to $645 million for Unum.[61]
31 December: Adcetris sales increase to $226 million.[62]

2016

For the year: the company was at the bottom of the Annual Top 25 Biotech Companies for the year as judged by staff of Genetic Engineering & Biotechnology News.[63]
28 March: the company announces it will develop 12 more drugs, employing another 100 staff.[62]

Product portfolio and pipeline

References

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  11. Seattle Genetics Initiates Pivotal Trial of SGN-35 for Hodgkin Lymphoma Corporate Press Release
  12. Seattle Genetics Initiates Phase II Trial of SGN-35 for Anaplastic Large Cell Lymphoma Corporate Press Release
  13. Seattle Genetics Initiates Brentuximab Vedotin (SGN-35) Retreatment Clinical Trial Corporate Press Release
  14. Seattle Genetics Achieves Milestone Under Antibody-Drug Conjugate Collaboration with MedImmune Corporate Press Release
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  16. Seattle Genetics Achieves Milestone Under Antibody-Drug Conjugate Collaboration With Bayer Schering Pharma Corporate Press Release
  17. Seattle Genetics Announces Discontinuation of Dacetuzumab Phase IIb Diffuse Large B-Cell Lymphoma Clinical Trial Corporate Press Release
  18. Seattle Genetics Initiates Phase I Clinical Trial of Antibody-Drug Conjugate SGN-75 Corporate Press Release
  19. Seattle Genetics Announces Termination of Collaboration Agreement with Genentech for Dacetuzumab (SGN-40) Corporate Press Release
  20. Seattle Genetics Announces Antibody-Drug Conjugate Collaboration with GlaxoSmithKline Corporate Press Release
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  22. Seattle Genetics Achieves Milestone under Antibody-Drug Conjugate Collaboration with Genentech Corporate Press Release
  23. Seattle Genetics, Takeda and Millennium Announce Initiation of Phase III AETHERA Trial of Brentuximab Vedotin (SGN-35) for Post-Transplant Hodgkin Lymphoma Corporate Press Release
  24. Seattle Genetics to Receive $9.5 Million Payment from Genentech to Extend Antibody-Drug Conjugate Collaboration Corporate Press Release
  25. Seattle Genetics and Agensys, an Affiliate of Astellas, Announce Initiation of Phase I Clinical Trial of ASG-5ME for Pancreatic Cancer Corporate Press Release
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  28. Abstract 2436: AGS-16M8F is a novel antibody drug conjugate (ADC) for treating renal and liver cancers; Gudas JM, Torgov M, An Z, Jia XC, Morrison KJ, Morrison RK, Yang P, et al. Cancer Res April 15, 2010 70; 2436. Last Accessed: February 15, 2011
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  33. Seattle Genetics and Millennium Expand Antibody-Drug Conjugate Collaboration Corporate Press Release
  34. Seattle Genetics Announces Antibody-Drug Conjugate Collaboration with Abbott Corporate Press Release
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  40. Seattle Genetics and Oxford BioTherapeutics to Collaborate on Antibody-Drug Conjugates for Cancer Corporate Press Release
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  42. Agensys and Seattle Genetics Announce Interim Phase I Data from ASG-5ME Clinical Trial for Prostate Cancer Astellas Press Release
  43. Millennium and Seattle Genetics Initiate Global Phase 3 Trial of ADCETRIS™ in Patients with CD30-Expressing Relapsed Cutaneous T-cell Lymphoma Corporate Press Release
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  49. Seattle Genetics Receives FDA Orphan Drug Designation for ADCETRIS® (Brentuximab Vedotin) in Mycosis Fungoides Corporate Press Release
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  53. Seattle Genetics Initiates Phase 1 Trial of SGN-CD33A in Acute Myeloid Leukemia (AML) Corporate Press Release
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External links