European Commission Approves ALUNBRIG® (brigatinib) for ALK+ Non-Small Cell Lung Cancer in Patients Previously Treated with Crizotinib, Advancing Treatment Paradigm in Europe
TAKEDA PHARMA (TKPYY)
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Company Research
Source: Business Wire
– ALUNBRIG Demonstrated Unprecedented Median Progression-Free Survival of 16.7 Months and Overall Survival of 34.1 Months in the Post-Crizotinib Setting – – Approval Will Help Address Current Unmet Need in ALK+ NSCLC Treatment in the EU, Building Upon Approvals in the U.S. and Canada – CAMBRIDGE, Mass. & OSAKA, Japan--(BUSINESS WIRE)-- Takeda Pharmaceutical Company Limited (TSE: 4502) today announced that the European Commission (EC) granted marketing authorization for ALUNBRIG (brigatinib) as a monotherapy for the treatment of adult patients with anaplastic lymphoma kinase-positive (ALK+) advanced non-small cell lung cancer (NSCLC) previously treated with crizotinib. The decision follows a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) on September 20, 2018. “The introduction of targeted therapies has greatly improved the treatment of ALK+ NSCLC, yet
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