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Janssen Marks First Approval Worldwide for TECVAYLI?(teclistamab) with EC Authorisation of First-in-Class Bispecific Antibody for the Treatment of Patients with Multiple Myeloma

Teclistamab, an off-the-shelf (ready to use) subcutaneously administered therapy, induced deep and rapid responses in triple-class exposed patients with relapsed and refractory multiple myeloma1 The
United States Jenni Mildon Williamn Hait Maria Victoria Mateos Peter Lebowitz Edmond Chan

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Daiichi Sankyo: Quizartinib Marketing Authorization Application Validated by EMA for Treatment of Adult Patients with Newly Diagnosed FLT3-ITD Positive Acute Myeloid Leukemia

Submission based on QuANTUM-First results showing quizartinib plus chemotherapy significantly improved overall survival compared to chemotherapy alone Daiichi Sankyo (TSE: 4568) today announced
United States Zuccae Ann Masashi Kawase Simone Jendsch Dowe Ken Takeshita Daiichi Sankyo

European Commission approves Celltrion Healthcare's Vegzelma™ (CT-P16, biosimilar bevacizumab) for the treatment of multiple types of cancer

European Commission approves Celltrion Healthcare’s Vegzelma™ (CT-P16, biosimilar bevacizumab) for the treatment of multiple types of cancer ·         Vegzelma™ offers European patients living with certain types of breast, lung, renal, colon, rect...
Inch On Gwangyoksi South Korea United States New Orleans Bevacizumab Avastin Kevin Byoung Seo Choi

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