Press Releases Takeda Pharmaceutical Company Limited

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Delayed Japan Exchange Other stock markets 11:30:00 30/04/2024 am IST			5-day change	1st Jan Change
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26/04	EU Panel Backs Approval of Takeda’s Colorectal Cancer Drug	MT
26/04	Hutchmed notes CHMP's positive opinion for fruiquintinib approval	AN

Press Releases

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HUTCHMED Announces Positive CHMP Opinion for Fruquintinib in Previously Treated Metastatic Colorectal Cancer Received by Takeda	29/04	AQ
Takeda Receives Positive CHMP Opinion for Fruquintinib in Previously Treated Metastatic Colorectal Cancer	26/04	BU
U.S. FDA Approves Subcutaneous Administration of Takeda's ENTYVIO for Maintenance Therapy in Moderately to Severely Active Crohn's Disease	19/04	AQ
Takeda to Hold Fiscal Year 2023 Earnings Call on May 9	19/04	AQ
U.S. FDA Approves Subcutaneous Administration of Takeda’s ENTYVIO® (vedolizumab) for Maintenance Therapy in Moderately to Severely Active Crohn’s Disease	19/04	BU
Takeda Announces New U.S. Corporate Social Responsibility Program Partners to Build Equity through STEM Education and Access to Nutritional Food	08/04	BU
Takeda Announces Approval of ADZYNMA Intravenous Injection 1500 in Japan for Patients with Congenital Thrombotic Thrombocytopenic Purpura	27/03	AQ
Takeda Announces Candidates for Board of Directors at Upcoming Shareholders Meeting	27/03	BU
Takeda Announces Approval of ADZYNMA® Intravenous Injection 1500 (apadamtase alfa /cinaxadamtase alfa) in Japan for Patients with Congenital Thrombotic Thrombocytopenic Purpura (cTTP)	26/03	BU
Takeda Announces U.S. FDA Approval of Supplemental New Drug Application for ICLUSIG in Adult Patients with Newly Diagnosed Ph+ ALL	20/03	AQ
Takeda Announces U.S. FDA Approval of Supplemental New Drug Application (sNDA) for ICLUSIG® (ponatinib) in Adult Patients with Newly Diagnosed Ph+ ALL	19/03	BU
Takeda Announces Positive Topline Results from Phase 2 Study Evaluating Mezagitamab, a Potential Best-in-Class Anti-CD38 Monoclonal Antibody, for Primary Immune Thrombocytopenia	14/03	AQ
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	13/03	BU
Takeda and Biological E. Limited Collaborate to Accelerate Access to Dengue Vaccine in Endemic Areas	27/02	BU
Championing Rare Voices on Rare Disease Day	26/02	AQ
FDA Approves Takeda's EOHILIA, the First and Only Oral Treatment in the U.S. for Eosinophilic Esophagitis	13/02	AQ
FDA Approves Takeda’s EOHILIA (budesonide oral suspension), the First and Only Oral Treatment in the U.S. for Eosinophilic Esophagitis (EoE)	12/02	BU
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	09/02	BU
Takeda Announces FY2023 Q3 Results, On-track towards Full-Year Management Guidance with Strong Momentum in Growth and Launch Products	02/02	AQ
Takeda Announces Chief Financial Officer Succession	01/02	BU

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