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December 11th, 2017
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Articles published by Genmab A/S
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Genmab to Present New and Updated Results From Multiple Clinical Trials Evaluating Epcoritamab Across Various B-Cell Malignancies at the 2024 European Hematology Association (EHA) Congress
May 14, 2024
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
Genmab Announces Financial Results for the First Quarter of 2024
May 02, 2024
From
Genmab A/S
Via
GlobeNewswire
TIVDAK® (tisotumab vedotin-tftv) Receives U.S. FDA Approval to Treat Recurrent or Metastatic Cervical Cancer
April 29, 2024
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
PFE
TIVDAK® (tisotumab vedotin-tftv) Receives U.S. FDA Approval to Treat Recurrent or Metastatic Cervical Cancer
April 29, 2024
From
Genmab A/S
Via
GlobeNewswire
Genmab to Broaden and Strengthen Oncology Portfolio with Acquisition of ProfoundBio
April 03, 2024
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
Genmab to Broaden and Strengthen Oncology Portfolio with Acquisition of ProfoundBio
April 03, 2024
From
Genmab A/S
Via
GlobeNewswire
U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab (EPKINLY®) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma
February 27, 2024
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
Genmab Announces Initiation of Share Buy-Back Program
February 14, 2024
From
Genmab A/S
Via
GlobeNewswire
Genmab Publishes 2023 Annual Report
February 14, 2024
From
Genmab A/S
Via
GlobeNewswire
Tisotumab Vedotin Marketing Authorization Application Validated by European Medicines Agency for Treatment of Recurrent or Metastatic Cervical Cancer
February 02, 2024
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
PFE
TIVDAK® (tisotumab vedotin-tftv) Supplemental Biologics License Application Accepted for Priority Review by U.S. Food and Drug Administration for Patients with Recurrent or Metastatic Cervical Cancer
January 09, 2024
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
PFE
New Pivotal Data for Bispecific Antibody Epcoritamab (DuoBody® CD3xCD20) Demonstrates High Overall and Complete Responses in Patients with Hard-To-Treat Relapsed/Refractory Follicular Lymphoma (FL)
December 09, 2023
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
Genmab Announces Positive Regulatory Updates for Epcoritamab (EPKINLY®/TEPKINLY®) for the Treatment of Relapsed/Refractory Follicular Lymphoma
November 27, 2023
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
Major Shareholder Announcement
November 09, 2023
From
Genmab A/S
Via
GlobeNewswire
Major Shareholder Announcement
November 08, 2023
From
Genmab A/S
Via
GlobeNewswire
Genmab Announces Financial Results for the First Nine Months of 2023
November 07, 2023
From
Genmab A/S
Via
GlobeNewswire
Genmab Announces Multiple Abstracts to be Presented at the 65th Annual Meeting and Exposition of the American Society of Hematology (ASH)
November 02, 2023
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
Genmab Announces Net Sales of DARZALEX® (daratumumab) for Third Quarter of 2023
October 17, 2023
From
Genmab A/S
Via
GlobeNewswire
Genmab Announces European Commission Approval of TEPKINLY® (epcoritamab) for Adults with Relapsed or Refractory (R/R) Diffuse Large B-cell Lymphoma (DLBCL)
September 25, 2023
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
Genmab Announces European Commission Approval of TEPKINLY® (epcoritamab) for Adults with Relapsed or Refractory (R/R) Diffuse Large B-cell Lymphoma (DLBCL)
September 25, 2023
From
Genmab A/S
Via
GlobeNewswire
EPKINLY™ (epcoritamab) Approved by Japan Ministry of Health, Labour and Welfare as the First Bispecific Antibody to Treat Adults Patients with Certain Types of Relapsed or Refractory (R/R) Large B-Cell Lymphoma (LBCL)
September 25, 2023
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
Genmab and Seagen Announce That TIVDAK® (tisotumab vedotin-tftv) Met its Primary Endpoint of Improved Overall Survival in Patients with Recurrent or Metastatic Cervical Cancer Compared to Chemotherapy
September 04, 2023
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
SGEN
Genmab and Seagen Announce That TIVDAK® (tisotumab vedotin-tftv) Met its Primary Endpoint of Improved Overall Survival in Patients with Recurrent or Metastatic Cervical Cancer Compared to Chemotherapy
September 04, 2023
From
Genmab A/S
Via
GlobeNewswire
Genmab Announces Financial Results for the First Half of 2023
August 03, 2023
From
Genmab A/S
Via
GlobeNewswire
Genmab Updates 2023 Financial Guidance
July 27, 2023
From
Genmab A/S
Via
GlobeNewswire
Genmab Announces AbbVie Receives Positive CHMP Opinion for Epcoritamab (TEPKINLY®) for the Treatment of Adults with Relapsed/Refractory (R/R) Diffuse Large B-cell Lymphoma (DLBCL)
July 21, 2023
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
Genmab Announces AbbVie Receives Positive CHMP Opinion for Epcoritamab (TEPKINLY®) for the Treatment of Adults with Relapsed/Refractory (R/R) Diffuse Large B-cell Lymphoma (DLBCL)
July 21, 2023
From
Genmab A/S
Via
GlobeNewswire
Genmab Announces Net Sales of DARZALEX® (daratumumab) for Second Quarter of 2023
July 20, 2023
From
Genmab A/S
Via
GlobeNewswire
Genmab and AbbVie Announce Positive Topline Results from Phase 1/2 EPCORE™ NHL-1 Trial Evaluating Epcoritamab (DuoBody® CD3xCD20) in Patients with Relapsed/Refractory Follicular Lymphoma (FL)
June 27, 2023
From
Genmab A/S
Via
GlobeNewswire
Genmab Announces Multiple Abstracts to be Presented at the American Society of Clinical Oncology (ASCO) Annual Meeting and European Hematology Association (EHA) Congress
May 25, 2023
From
Genmab A/S
Via
Business Wire
Tickers
GMAB
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