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EMA approval · 2025-10-29

EMA Authorised: Rybrevant (amivantamab) — Janssen-Cilag International N.V.

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Summary

EMA authorised Rybrevant (amivantamab) for non-small cell lung cancer. The marketing authorization holder is Janssen-Cilag International N.V.

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Diseases / indications

Drugs mentioned

  • RYBREVANT (amivantamab-vmjw)

Snippet

Status: Authorised. Therapeutic area: Carcinoma, Non-Small-Cell Lung. MAH: Janssen-Cilag International N.V.. Decision date: 18/09/2025