EMA
approval
· 2026-01-20
EMA Authorised: Libtayo (cemiplimab) — Regeneron Ireland Designated Activity Company (DAC)
Summary
The European Medicines Agency authorised Libtayo (cemiplimab) for the treatment of cutaneous squamous cell carcinoma (CSCC). Regeneron Ireland Designated Activi…
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Diseases / indications
Drugs mentioned
Snippet
Status: Authorised. Therapeutic area: Carcinoma, Squamous Cell. MAH: Regeneron Ireland Designated Activity Company (DAC). Decision date: 17/11/2025