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Takeda (TAK) Receives Positive CHMP Opinion for Recombinant ADAMTS13 (rADAMTS13) in Congenital Thrombotic Thrombocytopenic Purpura
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Takeda Provides Update on EXKIVITY® (mobocertinib)
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Takeda Pharmaceutical (TAK) Reports Favorable Phase 3 Safety and Efficacy Results of TAK-755
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Takeda Receives Positive CHMP Opinion Recommending Approval of Dengue Vaccine Candidate in EU and Dengue-Endemic Countries
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Takeda Pharmaceutical (TAK) Announces Publication of SOLSTICE Phase 3 Trial for LIVTENCITY in Post-Transplant Recipients With Cytomegalovirus Infection
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Takeda's (TAK) EXKIVITY Approved by U.S. FDA as First Oral Therapy Specifically Designed for Patients with EGFR Exon20 Insertion+ NSCLC
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