🇪🇺 PORFIMER SODIUM in European Union

EMA authorised PORFIMER SODIUM on 25 March 2004

Marketing authorisation

EMA — authorised 25 March 2004

  • Application: EMEA/H/C/000493
  • Marketing authorisation holder: Pinnacle Biologics B.V.
  • Local brand name: PhotoBarr
  • Indication: Photodynamic therapy (PDT) with PhotoBarr is indicated for: Ablation of high-grade dysplasia (HGD) in patients with Barrett's Oesophagus (BO)
  • Status: withdrawn

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PORFIMER SODIUM in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is PORFIMER SODIUM approved in European Union?

Yes. EMA authorised it on 25 March 2004.

Who is the marketing authorisation holder for PORFIMER SODIUM in European Union?

Pinnacle Biologics B.V. holds the EU marketing authorisation.