Tasonermin

Tasonermin (Beromun, Belpharma s.a.) has 1 EU-approved indication in 1 tumour type.
Approved indications of Tasonermin
Biomarker requirementRegimenSettingConditions
Soft tissue sarcoma1
None
+ melphalan via mild hyperthermic isolated limb perfusion (ILP)
Any line
advanced
As an adjunct to surgery for subsequent removal of the tumour to prevent or delay amputation, or in the palliative situation
Full text of section 4.1 (therapeutic indications)

Beromun is indicated in adults. as an adjunct to surgery for subsequent removal of the tumour so as to prevent or delay amputation, or in the palliative situation, for irresectable soft tissue sarcoma of the limbs, used in combination with melphalan via mild hyperthermic isolated limb perfusion (ILP).

Label history

18 changes to the Beromun label since 1999, none of them to the indications. Newest first, in the words of EMA's record of each procedure.

Changes