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EMA approval · 2026-03-24

EMA Authorised: Sylvant (siltuximab) — Recordati Netherlands B.V.

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Summary

The European Medicines Agency has authorized Sylvant (siltuximab) for giant lymph node hyperplasia (Castleman disease) with accelerated assessment; the marketin…

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Diseases / indications

Drugs mentioned

  • Sylvant (siltuximab)

Snippet

Status: Authorised. Therapeutic area: Giant Lymph Node Hyperplasia. MAH: Recordati Netherlands B.V.. Decision date: 24/03/2026. Accelerated assessment