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EMA approval · 2026-01-30

EMA Authorised: Qdenga (Dengue virus, serotype 2, expressing Dengue virus, serotype 1, surface proteins, live, attenuated;Dengue virus, serotype 2, expressing Dengue virus, serotype 3, surface proteins, live, attenuated;Dengue virus, serotype 2, expressing Dengue virus, serotype 4, surface proteins, live, attenuated;Dengue virus, serotype 2, live, attenuated) — Takeda Pharmaceuticals International AG Ireland Branch

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Summary

The European Medicines Agency authorised Qdenga, a live attenuated tetravalent dengue vaccine from Takeda, for protection against dengue disease in the European…

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Diseases / indications

Drugs mentioned

  • Qdenga (TAK-003)

Snippet

Status: Authorised. Therapeutic area: Dengue. MAH: Takeda Pharmaceuticals International AG Ireland Branch. Decision date: 19/12/2025