http://www.twitter.comTwitter is a service for friends, family, and co-workers to communicate and stay connected through the exchange of quick, frequent answers to one simple question: What are you doing?
View Older Stories View More Recent Stories
-
Genmab (GMAB) and AbbVie (ABBV) Announce Topline Results for Epcoritamab From Phase 1/2 Trial in Patients with R/R LBCL
-
Genmab and AbbVie Announce Topline Results for Epcoritamab (DuoBody®-CD3xCD20) From Phase 1/2 Trial in Patients with Relapsed/Refractory Large B-cell Lymphoma (LBCL)
-
Genmab and AbbVie Announce Topline Results for Epcoritamab (DuoBody®-CD3xCD20) From Phase 1/2 Trial in Patients with Relapsed/Refractory Large B-cell Lymphoma (LBCL)
-
Genmab and AbbVie Announce Topline Results for Epcoritamab (DuoBody®-CD3xCD20) From Phase 1/2 Trial in Patients with Relapsed/Refractory Large B-cell Lymphoma (LBCL)
-
Genmab A/S (GMAB) Announces Initial Resolution of Arbitration with Janssen Relating to Daratumumab License Agreement
-
Genmab Announces the Initial Resolution of its Arbitration with Janssen Relating to their Daratumumab License Agreement
-
Genmab Announces the Initial Resolution of its Arbitration with Janssen Relating to their Daratumumab License Agreement
-
Transactions with shares and linked securities in Genmab A/S made by managerial employees and their closely associated persons
-
Genmab (GMAB) and Abbvie (ABBV) Granted FDA Orphan-Drug Designation to Epcoritamab
-
Genmab Announces U.S. Food and Drug Administration Granted Orphan-Drug Designation to Epcoritamab (DuoBody®-CD3xCD20) in Follicular Lymphoma
-
Genmab Announces Appointments of Birgitte Stephensen to Chief Legal Officer and Chris Cozic to Chief People Officer
-
Transactions with shares and linked securities in Genmab A/S made by managerial employees and their closely associated persons
-
Genmab A/S (GMAB) and Seagen (SGEN) Report Data on Tisotumab Vedotin in Patients with Head and Neck Squamous Cell Carcinoma
-
Genmab and Seagen Present First Data on Tisotumab Vedotin (TIVDAK®) in Patients with Head and Neck Squamous Cell Carcinoma
-
Seagen and Genmab Present First Data on Tisotumab Vedotin (TIVDAK®) in Patients with Head and Neck Squamous Cell Carcinoma
-
Genmab and Seagen Present First Data on Tisotumab Vedotin (TIVDAK®) in Patients with Head and Neck Squamous Cell Carcinoma
-
Notice to Convene the Annual General Meeting of Genmab A/S
-
Genmab Files Annual Report with the U.S. Securities and Exchange Commission
-
Genmab Publishes 2021 Annual Report
-
Transactions with shares and linked securities in Genmab A/S made by managerial employees and their closely associated persons
-
Genmab A/S (GMAB) Reports 2021 Net Sales of DARZALEX of $6.02B
-
Genmab Announces Net Sales of DARZALEX® (daratumumab) for 2021
-
Genmab A/S (GMAB) and Synaffix Enter into License Agreement for ADC Technology
-
Genmab and Synaffix Enter into License Agreement for ADC Technology
-
Genmab and Synaffix Enter into License Agreement for ADC Technology
-
Genmab and Synaffix Enter into License Agreement for ADC Technology
-
Transactions with shares and linked securities in Genmab A/S made by managerial employees and their closely associated persons
-
Genmab Improves its 2021 Financial Guidance
-
Genmab Announces Multiple Abstracts to be Presented at the 63rd Annual Meeting and Exposition of the American Society of Hematology (ASH)
-
Genmab Announces Multiple Abstracts to be Presented at the 63rd Annual Meeting and Exposition of the American Society of Hematology (ASH)
-
Genmab (GMAB) Announces Net Sales of DARZALEX® (daratumumab) for the Third Quarter of 2021
-
Genmab Announces Net Sales of DARZALEX® (daratumumab) for the Third Quarter of 2021
-
Genmab Announces Abstracts Evaluating Investigational Solid Tumor Therapies to be Presented at the Society for Immunotherapy of Cancer’s 36th Annual Meeting (SITC 2021)
-
Genmab Announces Abstracts Evaluating Investigational Solid Tumor Therapies to be Presented at the Society for Immunotherapy of Cancer’s 36th Annual Meeting (SITC 2021)
-
Capital Increase in Genmab as a Result of Employee Warrant Exercise
-
Genmab and Seagen Announce FDA Accelerated Approval for TIVDAK™ (tisotumab vedotin-tftv) in Previously Treated Recurrent or Metastatic Cervical Cancer
-
Seagen (SGEN), Genmab Announce FDA Accelerated Approval for TIVDAK in Previously Treated Recurrent or Metastatic Cervical Cancer
-
Genmab and Seagen Announce FDA Accelerated Approval for TIVDAK™ (tisotumab vedotin-tftv) in Previously Treated Recurrent or Metastatic Cervical Cancer
-
Seagen and Genmab Announce FDA Accelerated Approval for TIVDAK™ (tisotumab vedotin-tftv) in Previously Treated Recurrent or Metastatic Cervical Cancer
-
Genmab and Seagen Announce FDA Accelerated Approval for TIVDAK™ (tisotumab vedotin-tftv) in Previously Treated Recurrent or Metastatic Cervical Cancer
-
Seagen (SGEN) and Genmab (GMAB) Present Encouraging Results From Two Cohorts of Phase 1b/2 innovaTV 205 Trial
-
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
-
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
-
Clinical Trial of Investigational Epcoritamab (DuoBody®-CD3xCD20) in Patients with Relapsed/Refractory B-cell non-Hodgkin’s Lymphoma (B-NHL) Published in The Lancet
-
Clinical Trial of Investigational Epcoritamab (DuoBody®-CD3xCD20) in Patients with Relapsed/Refractory B-cell Non-Hodgkin's Lymphoma (B-NHL) Published in The Lancet
-
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
-
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
-
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
-
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
-
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

