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TOKYO (dpa-AFX) - Takeda (TAK) announced the European Commission granted marketing authorization for the company's dengue vaccine QDENGA for the prevention of dengue disease in individuals from ....
The European Commission Approved QDENGA (TAK-003) for Use in Individuals Four Years of Age and Olderi QDENGA Becomes the Only Dengue Vaccine Approved in the EU for Use in Individuals Regardless of Previous ....
TOKYO (dpa-AFX) - Takeda (TAK) said that the U.S. Food and Drug Administration has granted priority review of the Biologics License Application for TAK-003, the company's investigational dengue ....