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FDA accepts Takeda's zasocitinib drug application for plaque psoriasis
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Takeda Announces Approval of LIVTENCITY® (maribavir) in Japan for Post-Transplant Cytomegalovirus (CMV) Infection/Disease That Is Refractory to Existing Anti-CMV Therapies
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Takeda Pharmaceutical (TAK) Announces FDA Approval of ADZYNMA
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Takeda Pharmaceutical (TAK) Reinforces Long-term Growth Through Pipeline Advancement and Two Targeted Acquisitions, Reports Q3
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Takeda’s Biologics License Application (BLA) for Dengue Vaccine Candidate (TAK-003) Granted Priority Review by U.S. Food and Drug Administration
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Takeda’s Dengue Vaccine Candidate Provides Continued Protection Against Dengue Fever Through 4.5 Years in Pivotal Clinical Trial
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Takeda’s LIVTENCITYTM (maribavir) Approved by U.S. FDA as the First and Only Treatment for People Ages 12 and Older with Post-Transplant Cytomegalovirus (CMV), Refractory (With or Without Genotypic
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