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Takeda Pharmaceutical Ltd ADR
(NY:
TAK
)
14.21
-0.10 (-0.70%)
Streaming Delayed Price
Updated: 10:01 AM EDT, Oct 11, 2024
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Press Releases about Takeda Pharmaceutical Ltd ADR
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CENTOGENE Extends Strategic Partnership With Takeda to Continue Providing Access to Genetic Testing for Patients With Lysosomal Storage Disorders
March 19, 2024
From
Centogene NV
Via
GlobeNewswire
Takeda Announces Positive Topline Results from Phase 2 Study Evaluating Mezagitamab (TAK-079), a Potential Best-in-Class Anti-CD38 Monoclonal Antibody, for Primary Immune Thrombocytopenia
March 13, 2024
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda and Biological E. Limited Collaborate to Accelerate Access to Dengue Vaccine in Endemic Areas
February 26, 2024
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
FDA Approves Takeda’s EOHILIA (budesonide oral suspension), the First and Only Oral Treatment in the U.S. for Eosinophilic Esophagitis (EoE)
February 12, 2024
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Intends to Rapidly Initiate the First Global Phase 3 Trials of TAK-861, an Oral Orexin Agonist, in Narcolepsy Type 1 in First Half of Fiscal Year 2024
February 08, 2024
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Announces Chief Financial Officer Succession
February 01, 2024
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Announces Third-Quarter FY2023 Results; On-Track Towards Full-Year Management Guidance With Strong Momentum in Growth & Launch Products
February 01, 2024
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda’s GAMMAGARD LIQUID® Approved by U.S. FDA for Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
January 29, 2024
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda’s HYQVIA® Approved by European Commission as Maintenance Therapy in Patients with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
January 29, 2024
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Named Global Top Employer for Seventh Consecutive Year
January 18, 2024
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Time to buy these 3 healthcare companies that raised revenue guidance?
January 16, 2024
The new year brings a clean slate heading into the fourth-quarter earnings season. Check out a few companies that have raised revenue guidance.
Via
MarketBeat
U.S. FDA Approves Takeda’s HYQVIA® as Maintenance Therapy in Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
January 16, 2024
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Announces China NMPA Approval of LIVTENCITY® (maribavir) for the Treatment of Adults With Post-transplant Cytomegalovirus (CMV) Refractory to Prior Therapies
December 21, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Receives Positive CHMP Opinion for HYQVIA® as Maintenance Therapy in Patients with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
December 15, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda and The New York Academy of Sciences Announce 2024 Innovators in Science Award Winners
December 05, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda to Present Data at 65th American Society of Hematology (ASH) Annual Meeting, Demonstrating Continued Commitment to Patients with Hematologic Diseases
November 27, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda’s ADZYNMA (ADAMTS13, recombinant-krhn) Approved by U.S. FDA as the First and Only Recombinant ADAMTS13 Enzyme Replacement Therapy for the Treatment of Congenital Thrombotic Thrombocytopenic Purpura (cTTP)
November 09, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Receives U.S. FDA Approval of FRUZAQLA™ (fruquintinib) for Previously Treated Metastatic Colorectal Cancer
November 08, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Announces Late-Breaking Data from Phase 2b Study of TAK-279, an Investigational, Oral, Once-Daily TYK2 Inhibitor, in Patients with Active Psoriatic Arthritis at American College of Rheumatology Convergence Annual Meeting
November 07, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Announces FY2023 H1 Results; Updates Full-Year Forecasts While Remaining on Track Towards Management Guidance
October 26, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
European Commission Approves ADCETRIS® (brentuximab vedotin) for the Treatment of Adult Patients with Previously Untreated CD30+ Stage III Hodgkin Lymphoma in Combination with AVD
October 18, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Settles Tax Dispute with Irish Revenue over Break Fee Received by Shire
October 17, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Announces Topline Results of Phase 3 ADMIRE-CD II Trial of Alofisel® (darvadstrocel) in Complex Crohn’s Perianal Fistulas
October 17, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda’s Dengue Vaccine Recommended by World Health Organization Advisory Group for Introduction in High Dengue Burden and Transmission Areas in Children Ages Six to 16 Years
October 03, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Provides Update on EXKIVITY® (mobocertinib)
October 02, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
HUTCHMED Announces Submission of New Drug Application for Fruquintinib for Previously Treated Metastatic Colorectal Cancer in Japan
September 29, 2023
— Third major market authorization application based on data from the FRESCO-2 global Phase III trial —
From
HUTCHMED (China) Limited
Via
GlobeNewswire
U.S. FDA Approves Subcutaneous Administration of Takeda's ENTYVIO® (vedolizumab) for Maintenance Therapy in Moderately to Severely Active Ulcerative Colitis
September 27, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Announces Approval of CUVITRU™ Subcutaneous Immunoglobulin in Japan for Patients with Agammaglobulinemia or Hypogammaglobulinemia
September 25, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Announces FDA Acceptance of NDA Resubmission of TAK-721 (budesonide oral suspension) for the Short-Term Treatment of Eosinophilic Esophagitis (EoE)
September 20, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
Takeda Commits Over $30 Million in Five New Global CSR Partnerships To Further Drive Health Impact in 92 Countries
September 13, 2023
From
Takeda Pharmaceutical Company Limited
Via
Business Wire
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