Takeda Announces Approval of HYQVIA® 10% S.C. (Subcutaneous) Injection Set in Japan for Patients with Agammaglobulinemia or Hypogammaglobulinemia

Osaka, Japan & Cambridge, Mass., United States:   HYQVIA [Immune Globulin Infusion 10% (Human) with Recombinant Human Hyaluronidase] is the

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Takeda Spotlights High-Value, Late-Stage Pipeline Accelerating the Development of Potential Transformative Treatments for Patients in Multiple Therapeutic Areas

Osaka, Japan & Cambridge, Mass., United States:    Six Late-Stage Programs with Peak Revenue Potential of $10B – $20B1 Poised

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Takeda Strengthens Oncology Pipeline with Elritercept through Licensing Agreement with Keros Therapeutics

Osaka, Japan & Cambridge, Mass., United States:   − Elritercept is a late-stage, potentially best-in-class activin inhibitor designed to treat anemia

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Takeda Announces Strong First Half FY2024 Results and Raises Full Year Outlook

Osaka, Japan:    Revenue Growth of +13.4% at Actual Exchange Rates (AER); +5.0% at Constant Exchange Rate (CER) Driven by

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Takeda Receives Approval for FRUZAQLA (fruquintinib) in Japan for the Treatment of Unresectable Advanced or Recurrent Colorectal Cancer

Osaka, Japan & Cambridge, Mass., United States:   − Approval Based on Results from Positive, Global, Phase 3 FRESCO-2 Trial −

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Takeda to Present Additional Clinical Trial Study Data Highlighting the Impact of Orexin Agonist TAK-861 on the Burden of Narcolepsy at Sleep Europe 2024

Osaka, Japan & Cambridge, Mass., United States:   − Presentations Include New Data from the TAK-861-2001 Phase 2b Trial in

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Takeda Commits Over $32 Million in Five New Global Corporate Social Responsibility Partnerships to Further Drive Health Impact in 93 Countries

Osaka, Japan & Cambridge, Mass., United States:   More Than 22,000 Takeda Employees Selected the FY2024 New Partners: Population Services

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