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FDA Approval Sought for Frontline Tislelizumab in Locally Advanced or Metastatic ESCC

The FDA has accepted for review a biologics license application seeking the approval of tislelizumab for use in the frontline treatment of patients with unresectable, recurrent, locally advanced or metastatic esophageal squamous cell carcinoma.
Mark Lanasa Solid Tumors At Beigene Ltd Map European Commission Solid Tumors Esophageal Squamous Cell Carcinoma Biologics License Application

BeiGene Strengthens Global Portfolio and Regains Full Rights from Novartis for Anti-PD-1 Antibody TEVIMBRA (tislelizumab)

19.09.2023 - BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160; SSE: 688235), a global biotechnology company, today announced that it has entered into an agreement with Novartis to regain worldwide rights to develop, manufacture, and commercialize TEVIMBRA ... Seite 1
Mark Lanasa Chief Medical Officer Solid Tumors Beigene Chart Eigene Kurs Eigene Aktie

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Two Florida Cancer Specialists & Research Institute Manuscripts Published in the New England Journal of Medicine Within Two Months

FCS Director of Drug Development Manish Patel, MD Co-Authors BothFORT MYERS, Fla., Sept. 15, 2023 /PRNewswire/ -- Florida Cancer Specialists & Res...
United States Lucion Gordan Amd Co Florida Cancer Specialists Research Institute American Society Of Clinical Oncology Drug Development Manish Patel

European Approval Sought for Erdafitinib in Locally Advanced or Metastatic FGFR3+ Urothelial Carcinoma

A marketing authorization application has been submitted to the European Medicines Agency seeking the approval of erdafitinib for the treatment of adult patients with locally advanced, unresectable or metastatic urothelial carcinoma harboring susceptible FGFR3 alterations who experienced disease progression during or following at least 1 line of therapy containing a PD-1/PD-L1 inhibitor.
Martin Vogel Janssen Cilag Gmb Kiran Patel Clinical Development Drug Administration Janssen Research Development

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