FDA
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FDA accepts rusfertide application with priority review for blood disorder
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Protagonist and Takeda report 52-week rusfertide data in polycythemia vera
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Takeda partners with Innovent for $1.2 billion oncology deal
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Takeda Announces First-Quarter FY2025 Results With Significant Late-Stage Pipeline Progression
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European Commission Approves ADCETRIS® (brentuximab vedotin) for the Treatment of Adult Patients with Newly Diagnosed Stage IIb/III/IV Hodgkin Lymphoma in Combination with ECADD
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Protagonist and Takeda Announce Positive Topline Results from Phase 3 VERIFY Study of Rusfertide in Patients with Polycythemia Vera
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Ligand Reports Second Quarter 2024 Financial Results
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