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Articles published by Takeda Pharmaceutical Company Limited

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Takeda Announces FY2026 First-Half Results Highlighting Launch Momentum and Pipeline Milestones
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Announces Arcotatug Tavatecan (TAK-921) Demonstrated Statistically Significant and Clinically Meaningful Improvements in Overall Survival and Progression-Free Survival in Phase 3 Advanced Gastric Cancer Study
From Takeda Pharmaceutical Company Limited
Via Business Wire
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First and Only Ulcerative Colitis Treat-to-Target Trial Shows Treating to Disease Clearance vs. Symptomatic Remission with ENTYVIO® (vedolizumab) Prolongs Time to First Disease-Related Complication
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda’s ORZEYFUL (oveporexton) Launches Simultaneously in Japan and China Giving Physicians First Access to Prescribe Novel Orexin Agonist to Patients with Narcolepsy Type 1
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Presents Phase 2/3 IgGNITE Study Results of Investigational Subcutaneous TAK-881 in Primary Immunodeficiency Disease (PID) at ESID 2026
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Zasocitinib Delivered Superior Efficacy Versus Deucravacitinib in New Phase 3 Head-to-Head Results, Reinforcing Potential to Deliver Rapid and Durable Skin Clearance in a Convenient Once-Daily Pill
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Highlights Late-Stage Oncology Pipeline Progress and Solid Tumor Portfolio Research, Led by Late-Breaking Phase 3 Arcotatug Tavatecan (TAK-921) Data, at ESMO 2026
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Employees Select Four New Global Corporate Social Responsibility Collaborations to Advance Climate-Resilient Health Systems
From Takeda Pharmaceutical Company Limited
Via Business Wire
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U.S. FDA Accepts New Drug Application Under Priority Review for Takeda’s Zasocitinib in Moderate-to-Severe Plaque Psoriasis, with Potential to Redefine Oral Treatment Expectations
From Takeda Pharmaceutical Company Limited
Via Business Wire
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New England Journal of Medicine Publishes Data from Phase 3 Studies Demonstrating Oveporexton (ORZEYFUL) Improved the Full Range of Narcolepsy Type 1 Symptoms and Quality of Life
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Receives U.S. FDA Approval of MIMRYLO™ (rusfertide), Marking a Potential Shift in the Treatment Paradigm for Polycythemia Vera
From Takeda Pharmaceutical Company Limited
Via Business Wire
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ORZEYFUL (oveporexton) Approved in Japan as the First and Only Medicine to Treat the Underlying Cause of Narcolepsy Type 1
From Takeda Pharmaceutical Company Limited
Via Business Wire
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U.S. FDA Approves Takeda’s ORZEYFUL™ (oveporexton), the First and Only Medicine to Treat the Underlying Cause of Narcolepsy Type 1
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Announces FY2026 First Quarter Results, Near-Term Launch Preparations and Pipeline Progress on Track
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda’s Zasocitinib Demonstrates Consistent, High Rates of Skin Clearance Across the Body, Including Hard-to-Treat and High-Impact Sites, in Phase 3 Psoriasis Studies
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda and the Indonesian Government Announce Landmark Collaboration to Strengthen Healthcare Resilience and Expand Access to Lifesaving Plasma-Derived Medicinal Products
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Announces New Assignments of Directors and Appointment of Julie Kim as Representative Director, President and CEO
From Takeda Pharmaceutical Company Limited
Via Business Wire
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New Pivotal Study Data Show Takeda’s Oveporexton Improved Daily Function, Cognition and Nighttime Sleep for People with Narcolepsy Type 1
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda’s Zasocitinib Significantly Outperforms Deucravacitinib in Head-to-Head Phase 3 Psoriasis Study, Promising to Redefine Oral Treatment Expectations
From Takeda Pharmaceutical Company Limited
Via Business Wire
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U.S. FDA Accepts Takeda's Application for Intravenous ENTYVIO® (vedolizumab) in Pediatric Ulcerative Colitis and Crohn's Disease
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Announces FY2025 Full Year Results and FY2026 Outlook, Highlighted by Excellent Pipeline Progress and Solid FY2025 Results
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Announces Positive Topline Results from Pivotal Phase 2/3 Clinical Trial of TAK-881 in Primary Immunodeficiency Disease (PID)
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda’s Zasocitinib Delivered Rapid and Durable Skin Clearance in a Convenient Once-Daily Pill, Affirming Promise to Reshape Psoriasis Care
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda and Protagonist Announce U.S. Food and Drug Administration Accepts New Drug Application and Grants Priority Review for Rusfertide as a Potential First-in-Class Therapy for Polycythemia Vera
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Positive Phase 3 Data Demonstrate Potential for ENTYVIO® (vedolizumab) to Address Treatment Gap for Children and Adolescents with Moderate to Severe Ulcerative Colitis
From Takeda Pharmaceutical Company Limited
Via Business Wire
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U.S. Food and Drug Administration Accepts New Drug Application and Grants Priority Review for Takeda’s Oveporexton (TAK-861) as a Potential First-in-Class Therapy for Narcolepsy Type 1
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Reports Third-Quarter FY2025 Results: Updates Full Year Outlook to Reflect VYVANSE® Generics Impact, OPEX Discipline and FX Tailwind; Progressing Toward Three Transformative Launches Ahead
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda Announces U.S. Availability of GAMMAGARD LIQUID ERC, the Only Ready-to-Use Liquid Immunoglobulin Therapy with Low Immunoglobulin A (IgA) Content1
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda and Protagonist Announce Submission of New Drug Application (NDA) for Rusfertide for Treatment of Polycythemia Vera (PV)
From Takeda Pharmaceutical Company Limited
Via Business Wire
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Takeda’s Zasocitinib Landmark Phase 3 Plaque Psoriasis Data Show Promise to Deliver Clear Skin in a Once-Daily Pill, Catalyzing a New Era of Treatment
From Takeda Pharmaceutical Company Limited
Via Business Wire
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