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Genmab A/S: U S FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab (EPKINLY) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma

Genmab A/S: U S FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab (EPKINLY) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma
finanznachrichten.de - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from finanznachrichten.de Daily Mail and Mail on Sunday newspapers.

United statesNew jerseyAndrew carlsenHematol hemoterDavid freundelGenmab us incData from the observational national lymphocare studyExposition of the american society hematologyDrug administrationLymphoma research foundationGlobal communications corporate affairsAbbvie biotechnology ltdExchange commissionPriority reviewBiologics license applicationPrescription drug user fee act

Genmab A/S: 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)

Genmab A/S: 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)
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United statesSan diegoFrance generalNew jerseyAndrew carlsenCatherine thieblemontHematol hemoterStefan klotterDavid freundelLymphoma research foundationAmerican society of hematologyExposition of the american society hematologyExchange commissionAbbvie biotechnology ltdData from the observational national lymphocare studyGenmab us inc

New Pivotal Data for Bispecific Antibody Epcoritamab (DuoBody® CD3xCD20) Demonstrates High Overall a

Data from the pivotal phase 1/2 EPCORE™ NHL-1 study showed 82 percent overall response rate (ORR), 63 percent complete response (CR) and 67 percent minimal residual disease (MRD) negativity in patients with relapsed/refractory (R/R) follicular lymphoma (FL) treated with subcutaneous epcoritamabResults presented at t.

San diegoUnited statesFrance generalNew jerseyAndrew carlsenHematol hemoterCatherine thieblemontDavid freundelAbbvie biotechnology ltdGlobal communications corporate affairsGenmab us incLymphoma research foundationAmerican society of hematologyExposition of the american society hematologyData from the observational national lymphocare studyParis university

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)

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)
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France generalUnited statesNew jerseySan diegoHematol hemoterDavid freundelCatherine thieblemontLymphoma research foundationExchange commissionData from the observational national lymphocare studyAbbvie biotechnology ltdExposition of the american society hematologyGenmab us incParis universityGlobal communications corporate affairsAnnual meeting

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)

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)
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New jerseyUnited statesSan diegoFrance generalCatherine thieblemontDavid freundelHematol hemoterParis universityAbbvie biotechnology ltdData from the observational national lymphocare studyLymphoma research foundationGlobal communications corporate affairsGenmab us incExposition of the american society hematologyExchange commissionAnnual meeting