Fighting dengue, where Sanofi stumbled, Takeda treads carefully
A new dengue vaccine, first approved in Indonesia, is to be evaluated by the US Food and Drug Administration under its Priority Review scheme.
Developed by Japanese pharma major Takeda (TYO:4502), TAK-003 is designed to prevent dengue disease caused by any dengue virus serotype in people aged between four and 60.
Marketed in Indonesia as Qdenga, the jab is part of a broad regulatory push from Takeda, with regulators at the European Medicines Agency already looking into an extensive data package.
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