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Genmab to Submit Biologics License Application to U S Food and Drug Administration for Epcoritamab (DuoBody®-CD3xCD20) for the Treatment of Relapsed/Refractory Large B-Cell Lymphoma (LBCL)

Genmab to Submit Biologics License Application to U S Food and Drug Administration for Epcoritamab (DuoBody®-CD3xCD20) for the Treatment of Relapsed/Refractory Large B-Cell Lymphoma (LBCL)
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New jerseyUnited statesKalvebod bryggeMarisol peronAndrew carlsenMacrophage propertiesj immunolDrug administrationExchange commissionHodgkin lymphoma research foundationMeeting of the european hematology associationDevelopment of novel antiCorporate affairsDiffuse large lymphoma research foundationCompany announcementWall streetPresidential symposium

Genmab to Submit Biologics License Application to U S Food

Company Announcement COPENHAGEN, Denmark; June 30, 2022 – Genmab A/S (Nasdaq: GMAB) today announced its intent to submit a biologics license application.

New jerseyUnited statesKalvebod bryggeMarisol peronAndrew carlsenMacrophage propertiesj immunolDrug administrationExchange commissionHodgkin lymphoma research foundationMeeting of the european hematology associationDevelopment of novel antiCorporate affairsDiffuse large lymphoma research foundationCompany announcementPresidential symposiumAnnual meeting

Genmab to Submit Biologics License Application to U S Food and Drug Administration for Epcoritamab (DuoBody®-CD3xCD20) for the Treatment of Relapsed/Refractory Large B-Cell Lymphoma (LBCL)

New jerseyUnited statesMarisol peronGenmaba skalvebod bryggeAndrew carlsenMacrophage propertiesj immunolDrug administrationExchange commissionHodgkin lymphoma research foundationMeeting of the european hematology associationDevelopment of novel antiDiffuse large lymphoma research foundationCompany announcementPresidential symposiumAnnual meetingEuropean hematology association

Genmab Announces Late-Breaking Phase 2 Trial Results of Investigational Epcoritamab (DuoBody®-CD3xCD

Epcoritamab demonstrated clinically meaningful efficacy in challenging to treat, highly refractory LBCL patients, including patients previously treated with chimeric antigen receptor (CAR) T-cell therapyTotal patient population achieved overall response rate (ORR) of 63 percent and complete response (CR) of 39 perce.

France generalNew jerseyUnited statesDavid freundelCatherine thieblemontProduct communicationsMacrophage propertiesj immunolAbbvie biotechnology ltdExchange commissionHodgkin lymphoma research foundationMeeting of the european hematology associationDevelopment of novel antiOncology departmentDiffuse large lymphoma research foundationPresidential symposiumAnnual meeting

Genmab Announces Late-Breaking Phase 2 Trial Results of Investigational Epcoritamab (DuoBody-CD3xCD20) in Relapsed/Refractory Large B-cell Lymphoma (LBCL) Patients Presented at European Hematology Association (EHA) Presidential Symposium

Epcoritamab demonstrated clinically meaningful efficacy in challenging to treat, highly refractory LBCL patients, including patients previously treated with chimeric antigen receptor (CAR) T-cell

France generalNew jerseyUnited statesDavid freundelCatherine thieblemontAndrew carlsenProduct communicationsMacrophage propertiesj immunolAbbvie biotechnology ltdExchange commissionHodgkin lymphoma research foundationMeeting of the european hematology associationDevelopment of novel antiOncology departmentDiffuse large lymphoma research foundationPresidential symposium