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Seagen and Genmab Announce FDA Accelerated Approval for TIVDAK™ (tisotumab vedotin-tftv) in Previously Treated Recurrent or Metastatic Cervical Cancer
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Seagen (SGEN) and Genmab (GMAB) Present Encouraging Results From Two Cohorts of Phase 1b/2 innovaTV 205 Trial
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Genmab and Seagen Present Interim Results From the innovaTV 205 Study for Tisotumab Vedotin Combination Therapy Treatment of Recurrent or Metastatic Cervical Cancer at ESMO Virtual Congress 2021
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Seagen and Genmab Present Interim Results From the innovaTV 205 Study for Tisotumab Vedotin Combination Therapy Treatment of Recurrent or Metastatic Cervical Cancer at ESMO Virtual Congress 2021
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Seagen to Present at the Morgan Stanley 19th Annual Global Healthcare Conference
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Seagen to Highlight Research From 16 Presentations Across Multiple Tumor Types at ESMO 2021
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Seagen and RemeGen Announce Exclusive Worldwide License and Co-Development Agreement for Disitamab Vedotin
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Seagen Reports Second Quarter 2021 Financial Results
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Astellas, Seagen (SGEN) Announce U.S. FDA Grants Regular Approval and Expands Indication for PADCEV for Patients with Locally Advanced or Metastatic Urothelial Cancer
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U.S. FDA Grants Regular Approval and Expands Indication for PADCEV® (enfortumab vedotin-ejfv) for Patients with Locally Advanced or Metastatic Urothelial Cancer
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U.S. FDA Grants Regular Approval and Expands Indication for PADCEV® (enfortumab vedotin-ejfv) for Patients with Locally Advanced or Metastatic Urothelial Cancer
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Seagen to Host Conference Call and Webcast Discussion of Second Quarter 2021 Financial Results on July 29, 2021
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SpringWorks Therapeutics (SWTX) Announces Clinical Collaboration with Seagen (SGEN) to Evaluate Nirogacestat in Combination with SEA-BCMA in Patients with R/R Multiple Myeloma
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Seagen (SGEN) Announces Long-Term Results from TUKYSA Pivotal Trial in Patients with HER2-Positive Breast Cancer During ASCO
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Seagen Announces Long-Term Results from TUKYSA® (tucatinib) Pivotal Trial in Patients with HER2-Positive Breast Cancer During the Virtual Scientific Program of the 2021 ASCO Annual Meeting
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Seagen to Present at the Goldman Sachs 42nd Annual Global Healthcare Conference
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Seagen (SGEN) and Astellas Pharma Inc. Report Updated Results from Two Trials of PADCEV (enfortumab vedotin-ejfv)
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Astellas and Seagen Announce Updated Results from Two Trials of PADCEV® (enfortumab vedotin-ejfv) in Patients with Locally Advanced or Metastatic Urothelial Cancer Not Eligible for Cisplatin Chemothe
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Seagen and Astellas Announce Updated Results from Two Trials of PADCEV® (enfortumab vedotin-ejfv) in Patients with Locally Advanced or Metastatic Urothelial Cancer Not Eligible for Cisplatin Chemothe
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Seagen Reports First Quarter 2021 Financial Results
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Seagen to Showcase Data from Growing Oncology Portfolio During Virtual Scientific Program of the 2021 ASCO Annual Meeting
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Astellas and Seagen (SGEN) Announce U.S. FDA Acceptance of Two SBLAs for PADCEV in Locally Advanced or Metastatic Urothelial Cancer
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Seagen and Astellas Announce U.S. FDA Acceptance of Two Supplemental Biologics License Applications for PADCEV® (enfortumab vedotin-ejfv) in Locally Advanced or Metastatic Urothelial Cancer
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Astellas and Seagen Announce U.S. FDA Acceptance of Two Supplemental Biologics License Applications for PADCEV® (enfortumab vedotin-ejfv) in Locally Advanced or Metastatic Urothelial Cancer
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Genmab A/S (GMAB) and Seagen (SGEN) Announce U.S. FDA Filing Acceptance for Priority Review of Tisotumab Vedotin BLA for Patients with Recurrent or Metastatic Cervical Cancer
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Seagen and Genmab Announce U.S. FDA Filing Acceptance for Priority Review of Tisotumab Vedotin Biologics License Application for Patients with Recurrent or Metastatic Cervical Cancer
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Genmab and Seagen Announce U.S. FDA Filing Acceptance for Priority Review of Tisotumab Vedotin Biologics License Application for Patients with Recurrent or Metastatic Cervical Cancer
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Genmab and Seagen Announce U.S. FDA Filing Acceptance for Priority Review of Tisotumab Vedotin Biologics License Application for Patients with Recurrent or Metastatic Cervical Cancer
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Seagen to Highlight Data from Novel Targeted Therapies at AACR
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Seagen to Host Conference Call and Webcast Discussion of First Quarter 2021 Financial Results on April 29, 2021
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Seagen Recommends Rejection Of 'Mini-Tender' Offer from TRC Capital Investment Corporation
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Seagen to Present at the Cowen 41st Annual Healthcare Conference
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Astellas and Seagen (SGEN) Announce Submission of Two sBLA to U.S. FDA for PADCEV in Locally Advanced or Metastatic Urothelial Cancer
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Seagen and Astellas Announce Submission of Two Supplemental Biologics License Applications to the U.S. FDA for PADCEV® (enfortumab vedotin-ejfv) in Locally Advanced or Metastatic Urothelial Cancer
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Astellas and Seagen Announce Submission of Two Supplemental Biologics License Applications to the U.S. FDA for PADCEV® (enfortumab vedotin-ejfv) in Locally Advanced or Metastatic Urothelial Cancer
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Astellas and Seagen (SGEN) Announce Presentation of Results from PADCEV Pivotal Trial in Patients with Previously Treated Advanced UC Who Were Ineligible for Cisplatin Chemotherapy
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Seagen and Astellas Announce Phase 3 Trial Results Demonstrating Survival Advantage of PADCEV® (enfortumab vedotin-ejfv) in Patients with Previously Treated Advanced Urothelial Cancer
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Astellas and Seagen Announce Phase 3 Trial Results Demonstrating Survival Advantage of PADCEV® (enfortumab vedotin-ejfv) in Patients with Previously Treated Advanced Urothelial Cancer
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Seagen and Astellas Announce Presentation of Results from PADCEV® (enfortumab vedotin-ejfv) Pivotal Trial in Patients with Previously Treated Advanced Urothelial Cancer Who Were Ineligible for Cispla
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Astellas and Seagen Announce Presentation of Results from PADCEV® (enfortumab vedotin-ejfv) Pivotal Trial in Patients with Previously Treated Advanced Urothelial Cancer Who Were Ineligible for Cispla
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Seagen (SGEN) Reports European Commission Approval of TUKYSA (tucatinib) for Treatment of Patients with Locally Advanced or Metastatic HER2-Positive Breast Cancer
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European Commission Approves Seagen’s TUKYSA® (tucatinib) for the Treatment of Patients with Locally Advanced or Metastatic HER2-Positive Breast Cancer
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Seagen Reports Fourth Quarter and Full Year 2020 Financial Results
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Seagen (SGEN), Genmab (GMAB) Submit Tisotumab Vedotin Biologics License Application to the U.S. FDA for Patients with Recurrent or Metastatic Cervical Cancer
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Seagen and Genmab Submit Tisotumab Vedotin Biologics License Application to the U.S. FDA for Patients with Recurrent or Metastatic Cervical Cancer
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Seagen to Host Conference Call and Webcast Discussion of Fourth Quarter and Full Year 2020 Financial Results on February 11, 2021
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Seagen to Present at the J.P. Morgan Healthcare Conference
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Alpine Immune Sciences Appoints Natasha Hernday to Board of Directors
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Seagen (SGEN) Announces Positive CHMP Opinion for TUKYSA for Treatment of Patients with Locally Advanced or Metastatic HER2-Positive Breast Cancer
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Seagen Announces Positive CHMP Opinion for TUKYSA® (tucatinib) for the Treatment of Patients with Locally Advanced or Metastatic HER2-Positive Breast Cancer

