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EMA approval · 2026-03-25

EMA Authorised: Tepezza (teprotumumab) — Amgen Europe B.V.

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Summary

The European Medicines Agency authorised Tepezza (teprotumumab) for Graves' ophthalmopathy, with Amgen Europe B.V. as the marketing authorization holder. This m…

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Diseases / indications

Drugs mentioned

  • TEPEZZA (teprotumumab)

Snippet

Status: Authorised. Therapeutic area: Graves Ophthalmopathy. MAH: Amgen Europe B.V.. Decision date: 25/03/2026