Takeda begins regulatory submissions for dengue vaccine candidate in the EU, Latin America, South America, South Asia and ASEAN
Takeda Pharmaceutical Company, a leading global biopharmaceutical with headquarters in Japan, announced that the European Medicines Agency (EMA) has accepted the Company’s filing packages for its dengue vaccine candidate (TAK-003), which is being investigated in the Phase 3 trial for the efficacy and safety in prevention of dengue due to any dengue virus serotypes in individuals aged 4–60 years.