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EMA approval · 2026-01-20

EMA Authorised: Imnovid (previously Pomalidomide Celgene) (Pomalidomide) — Bristol-Myers Squibb Pharma EEIG

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Summary

The EMA authorised Imnovid (pomalidomide) for use in multiple myeloma, with Bristol-Myers Squibb Pharma EEIG as the marketing authorization holder.

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Diseases / indications

Drugs mentioned

  • Imnovid (Pomalidomide)

Snippet

Status: Authorised. Therapeutic area: Multiple Myeloma. MAH: Bristol-Myers Squibb Pharma EEIG. Decision date: 21/08/2025