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TKDA

US8740602052

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 12:11:57 26/06/2024 BST 		5-day change 1st Jan Change
12.15 EUR +2.97% Intraday chart for Takeda Pharmaceutical Company Limited +2.59% -5.56%
06-25 US CDC alerts healthcare providers of increase in dengue cases RE
06-25 Takeda's Cancer Drug Gets European Commission Approval MT

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TAKEDA PHARMACEUTICAL : Form 6 K
PU
Takeda Pharmaceutical : Announces New Assignments of Directors Form 6 K
PU
Takeda Announces New Assignments of Directors
BU
US CDC alerts healthcare providers of increase in dengue cases
RE
Takeda's Cancer Drug Gets European Commission Approval
MT
Hutchmed China notes Takeda obtains EU approval for Fruzaqla
AN
Takeda's Organ Transplant Infection Treatment Approved by Japan Regulators
MT
Hutchmed (China), Takeda Secure EU Approval for Colorectal Cancer Treatment
MT
Takeda Announces Approval of LIVTENCITY® (maribavir) in Japan for Post-Transplant Cytomegalovirus (CMV) Infection/Disease That Is Refractory to Existing Anti-CMV Therapies
BU
Takeda Announces Approval of LIVTENCITY® by the Japanese Ministry of Health, Labour and Welfare
CI
Japanese Shares End Higher as BoJ Indicates Readiness for Policy Shifts
MT
Takeda Receives European Commission Approval for Colorectal Cancer Treatment
MT
Takeda Receives European Commission Approval for FRUZAQLA® (fruquintinib)
CI
Takeda Presents Late-Breaking Data from Phase 2b Study of Mezagitamab, Demonstrating Potential to Transform Treatment of Primary Immune Thrombocytopenia
BU
Takeda Presents Late-Breaking Data from Phase 2b Study of Mezagitamab, Demonstrating Potential to Transform Treatment of Primary Immune Thrombocytopenia
CI
Takeda Secures European Commission's Approval for Colorectal Cancer Drug Fruzaqla
MT
Takeda Pharmaceutical Gets European Commission Approval for Cancer Treatment
DJ
Takeda Receives Approval from European Commission for FRUZAQLA in Previously Treated Metastatic Colorectal Cancer
BU
Takeda Receives Approval from European Commission for Fruquintinib in Previously Treated Metastatic Colorectal Cancer
CI
Takeda's HyQvia® Approved as Replacement Therapy for Primary Humoral Immunodeficiency and Secondary Humoral Immunodeficiency in Pediatric Patients 2 years of Age and Older
AQ
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