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Atara Biotherapeutics' Ebvallo (tabelecleucel) Receives European Commission Approval as First Ever Therapy for Adults and Children with EBV+ PTLD Seite 1

19.12.2022 - Atara Biotherapeutics, Inc. (Nasdaq: ATRA) and Pierre Fabre today announced that the European Commission (EC) has granted marketing authorization for Ebvallo (tabelecleucel) as a monotherapy for the treatment of adult and pediatric patients two . Seite 1 ....

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Galapagos NV: Galapagos announces strategy to accelerate innovation and reports strong third quarter 2022 results

Clear path forward for accelerated growth and value creation Reshape innovation model and build fit-for-purpose organization in key strategic therapeutic areas: immunology and oncologyJyseleca 2022 ....

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Aeglea BioTherapeutics Reports Third Quarter 2022 Financial Results and Provides Program Updates

/PRNewswire/ Aeglea BioTherapeutics, Inc. (NASDAQ:AGLE), a clinical-stage biotechnology company developing a new generation of human enzyme therapeutics as. ....

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Investegate |Galapagos NV Announcements | Galapagos NV: Galapagos announces strategy to accelerate innovation and reports strong third quarter 2022 results

Investegate announcements from Galapagos NV, Galapagos announces strategy to accelerate innovation and reports strong third quarter 2022 results ....

New York , United States , Region Flamande , Perifereia Thessalias , United Kingdom , Czech Republic , Great Britain , Paul Stoffels , Van Gijsel , Bart Filius , Sandra Cauwenberghs , Marieke Vermeersch , Pharmacovigilance Risk Assessment Committee , Gilead Sciences , European Commission , Exchange Commission , Society Of Hematology , European Union , European Medicines Agency , Committee For Medicinal Products Human Use , Strategy Webcastpresentation , Authorization Application , Medicinal Products , Human Use , Annual Society , Non Hodgkin Lymphoma ,

GSK's application for its RSV vaccine accepted by EMA under accelerated assessment

GSK's application for its RSV vaccine accepted by EMA under accelerated assessment
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