🇪🇺 L19TNF in European Union

L19TNF (L19TNF) regulatory status in European Union.

Marketing authorisation

EMA

  • Application: EMEA/H/C/005651
  • Marketing authorisation holder: Philogen S.p.A.
  • Local brand name: Nidlegy
  • Indication: Neoadjuvant treatment of adult patients with locally advanced fully resectable melanoma 
  • Status: withdrawn

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Frequently asked questions

Is L19TNF approved in European Union?

Yes. EMA has authorised it.

Who is the marketing authorisation holder for L19TNF in European Union?

Philogen S.p.A. holds the EU marketing authorisation.