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EMA approval · 2024-12-17

EMA Authorised: Vizimpro (dacomitinib monohydrate) — Pfizer Europe MA EEIG

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Summary

The European Medicines Agency authorised Vizimpro (dacomitinib monohydrate) for non-small cell lung cancer, with Pfizer Europe MA EEIG as the marketing authoriz…

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Diseases / indications

Drugs mentioned

  • VIZIMPRO (dacomitinib)

Snippet

Status: Authorised. Therapeutic area: Carcinoma, Non-Small-Cell Lung. MAH: Pfizer Europe MA EEIG. Decision date: 11/12/2024