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Drug

Tasonermin

Approved · EMA
Also known as Tumor necrosis factor alfa-1a, Tumour necrosis factor alfa-1a, tasonermin (tumor necrosis fctr alfa-1a), Tasonermina+1 more

Tumor necrosis factor alfa-1a, Tumour necrosis factor alfa-1a, tasonermin (tumor necrosis fctr alfa-1a), Tasonermina, Tumor necrosis factor, soluble form, nonglycosylated.

RxNorm283746UNII23CA79S88F
1
Regulatory events
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this drug.

Approval: Beromun (EMA)

Regulatory1999-04-12EMA

Profile

Identifiers & mechanism

Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.

Canonical name
Tasonermin
Aliases & brands
Tumor necrosis factor alfa-1aTumour necrosis factor alfa-1atasonermin (tumor necrosis fctr alfa-1a)TasonerminaTumor necrosis factor, soluble form, nonglycosylated
RxNorm CUI
283746
UNII
23CA79S88F
Regulatory jurisdictions
ema

Regulatory timeline

1 event

The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.

Earliest approval
1999-04-12
Latest approval
1999-04-12
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
1999-04-12Approval
Approval: Beromun (EMA)
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 irresectableShow full 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).

Evidence ↗

Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.

References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • Regulatory event sources are credited in the Regulatory Timeline above.