Takeda

1449 articles about Takeda

• Takeda to Present Oncology Portfolio and Pipeline Data at the 2023 ASCO Annual Meeting and EHA Congress

  5/26/2023

  Takeda announced that it will present data from its expanding oncology pipeline and established product portfolio at the 59th Annual Meeting of the American Society of Clinical Oncology being held June 2-6, 2023, in Chicago, Ill.

• Takeda and HUTCHMED Announce New Drug Application (NDA) for Fruquintinib for Treatment of Previously Treated Metastatic Colorectal Cancer Granted Priority Review

  5/25/2023

  Takeda and HUTCHMED Limited announced that the U.S. Food and Drug Administration has granted priority review of the New Drug Application for fruquintinib, a highly selective and potent inhibitor of vascular endothelial growth factor receptors -1, -2 and -3 for the treatment of adult patients with previously treated metastatic colorectal cancer.

• U.S. Food & Drug Administration Grants Priority Review of TAK-755 for the Treatment of Congenital Thrombotic Thrombocytopenic Purpura (cTTP)

  5/16/2023

  Takeda (TSE: 4502/NYSE:TAK) today announced that the U.S. Food and Drug Administration (FDA) has accepted Takeda’s Biologics License Application (BLA) for TAK-755, an enzyme replacement therapy for the treatment of congenital thrombotic thrombocytopenic purpura (cTTP), an ADAMTS13 deficiency disorder.

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  Gout Disease Control Suffered After FDA-Driven Price Hike: Study

  5/11/2023

  Colchicine, a drug used to treat gout, saw a 16-fold price increase since the FDA changed its policy toward single-ingredient oral colchicine products, which had previously been available generically.

• Takeda Delivers Strong Revenue and Profit Growth in FY2022; Updated Capital Allocation Policy Reflects Deleveraging Progress and Confidence in Growth Outlook

  5/11/2023

  Takeda announced strong financial results for fiscal year 2022, delivering or exceeding management guidance, driven by the performance of its Growth & Launch Products.

• Innate Pharma Reports First Quarter 2023 Financial Results and Business Update

  5/10/2023

  Innate Pharma SA reported its consolidated financial results for the quarter ending March 31, 2023.

• Takeda Announces FDA Acceptance of BLA Resubmission for Investigational Subcutaneous Administration of Entyvio® (vedolizumab) for Maintenance Therapy in Moderately to Severely Active Ulcerative Colitis

  4/27/2023

  Takeda today announced that the U.S. Food and Drug Administration (FDA) has accepted for review its Biologics License Application (BLA) resubmission for the investigational subcutaneous (SC) administration of Entyvio® (vedolizumab) for maintenance therapy in adults with moderately to severely active ulcerative colitis (UC) after induction therapy with Entyvio intravenous.

• Long-term Safety & Efficacy Findings from Soticlestat Open Label Extension Study Presented by Takeda at American Academy of Neurology Annual Meeting

  4/27/2023

  Ovid Therapeutics Inc. reports that Takeda Pharmaceuticals presented interim data at the 2023 annual meeting of the American Academy of Neurology from ENDYMION 1, a long-term, open label extension study evaluating the effects of soticlestat on patients with Dravet syndrome and Lennox-Gastaut syndrome.

• Corza Medical Signs Definitive Agreement to Acquire Takeda's TachoSil Manufacturing Operations

  4/26/2023

  Corza Medical announced that it has entered into a definitive agreement with a subsidiary of Takeda Pharmaceuticals Company to acquire the TachoSil manufacturing operations in Linz, Austria.

• Celiac Disease Foundation, Takeda Announce Early Career Research Award in Celiac Disease

  4/25/2023

  The Celiac Disease Foundation, a world leader in patient advocacy, and Takeda Development Center Americas, a global biopharmaceutical leader, are proud to announce the Celiac Disease Foundation–Takeda Early Career Research Award; an award designed to attract promising researchers to the study of celiac disease.

• Adaptive Biotechnologies Announces Translational Collaboration with Takeda to Measure Minimal Residual Disease with Its clonoSEQ® Assay Across Its Hematologic Malignancy Pipeline

  4/12/2023

  Adaptive Biotechnologies Corporation today announced it has entered into a translational collaboration with Takeda to use its clonoSEQ ® Assay to assess minimal residual disease (MRD) to facilitate the development and commercialization of Takeda’s pipeline of treatments for patients with lymphoid malignancies.

• Treventis Partners its Preclinical Program in Alzheimer's Disease with Takeda

  4/11/2023

  Treventis Corporation, a privately held biotechnology company, announced today that it has entered an option, collaboration, and license agreement with Takeda for the further research, development, and commercialization of small molecules that target tau, a key protein in Alzheimer's Disease (AD).

• Takeda Receives FDA Approval to Expand the Use of HYQVIA® to Treat Primary Immunodeficiency in Children

  4/11/2023

  Takeda Receives FDA Approval to Expand the Use of HYQVIA ® to Treat Primary Immunodeficiency in Children.

• CENTOGENE Extends Strategic Partnership With Takeda to Continue Providing Access to Genetic Testing for Patients With Lysosomal Storage Disorders

  4/11/2023

  Centogene N.V., the essential life science partner for data-driven answers in rare and neurodegenerative diseases, announced it has extended its partnership with Takeda to diagnose patients with Lysosomal Storage Disorders.

• Takeda Announces New U.S. Corporate Social Responsibility (CSR) Program Partners

  4/3/2023

  Takeda announced that 21 new U.S. non-profit organizations have received grants as part of the company’s $19.5 million commitment to its FY2022 Corporate Social Responsibility program.

• Takeda Announces Candidates for Board of Directors at Upcoming Shareholders Meeting

  3/30/2023

  Takeda announced that its Board of Directors decided that it will propose a new candidate for independent external director at the 147th Ordinary Meeting of Shareholders on June 28th, 2023.

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  Takeda’s $4B Plaque Psoriasis Candidate Clears Mid-Stage Study

  3/20/2023

  Takeda will advance its experimental drug for plaque psoriasis, TAK-279, to Phase III later this year after the TYK2 inhibitor met its primary and secondary endpoints in a Phase IIb study.
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  Takeda Oncology Invests in Talent, Pipeline Growth Despite Turbulent Market

  3/20/2023

  In spite of a tumultuous economy, many life science companies have started the year off strong. With plans to expand its team and pipeline in the coming year, Takeda is one of them.

• Takeda Announces Positive Results in Phase 2b Study of Investigational TAK-279, an Oral, Once-Daily TYK2 Inhibitor, in People with Moderate-to-Severe Plaque Psoriasis

  3/18/2023

  Takeda announced positive results from a Phase 2b clinical trial of TAK-279, a highly selective, oral allosteric tyrosine kinase 2 inhibitor, in patients with moderate-to-severe plaque psoriasis.

• HUTCHMED Announces Closing of Fruquintinib License to Takeda Outside China

  3/14/2023

  HUTCHMED Limited announces that, further to its announcement on January 23, 2023 and following the completion of customary closing conditions including antitrust regulatory reviews, the exclusive license agreement with a subsidiary of Takeda Pharmaceutical Company Limited to further the global development, commercialization and manufacture of fruquintinib outside China has closed.