EU/3/20/2291: Orphan designation for the treatment of glioma

Onfekafusp alfa


On 26 June 2020, orphan designation EU/3/20/2291 was granted by the European Commission to Philogen S.p.A., Italy, for onfekafusp alfa for the treatment of glioma.

Key facts

Active substance
Onfekafusp alfa
Intended use
Treatment of glioma
Orphan designation status
EU designation number
Date of designation

Philogen S.p.A.
Piazza La Lizza 7
53100 Siena (SI)
Tel. +39 0577 1781632

Review of designation

The Committee for Orphan Medicinal Products reviews the orphan designation of a product if it is approved for marketing authorisation.

Documents related to this orphan designation evaluation

Patients' organisations

For contact details of patients’ organisations whose activities are targeted at rare diseases, see:

  • European Organisation for Rare Diseases (EURORDIS), a non-governmental alliance of patient organisations and individuals active in the field of rare diseases.

  • Orphanet, a database containing information on rare diseases, which includes a directory of patients’ organisations registered in Europe.

EU register of orphan medicines

The list of medicines that have received an orphan designation in the EU is available on the European Commission's website:

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