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EMA Product

Beromun

Product approved by European Medicines Agency (EU)

Basic Information

Beromun

Regulatory Information

EMEA/H/C/000206

Authorised

April 12, 1999

15

January 10, 2022

Company Information

Luxembourg

2, Rue Albert 1 er L-1117 Luxembourg

Belpharma Sa

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication 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).

Overview Summary

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the studies performed, to reach its recommendations on how to use the medicine. If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis of the CHMP recommendations, read the scientific discussion (also part of the EPAR).

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