The European Medicines Agency has validated a type II application for the investigational T-cell engaging bispecific antibody epcoritamab-bysp for patients with relapsed/refractory follicular lymphoma following at least 2 prior lines of therapy
BeiGene, Ltd : BeiGene to Present New Data Highlighting Hematology Portfolio and Pipeline Strengths at ASH 2023
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BeiGene to Present New Data Highlighting Hematology Portfolio and Pipeline Strengths at ASH 2023
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Abbvie Announces U S Food And Drug Administration (FDA) And European Medicines Agency (EMA) Updates For Epcoritamab (EPKINLY®/TEPKINLY®) For The Trea
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