Catalyst Wire Dossier Catalyst Wire Dossier
EMA approval · 2026-08-20

EMA Authorised: Xolremdi (mavorixafor) — Norgine B.V.

View source ↗

Summary

Xolremdi (mavorixafor) has been authorised in the EU for primary immunodeficiency diseases by Norgine B.V. (orphan medicine).

Upgrade for the full analysis, importance score, and drug timeline.

Diseases / indications

Drugs mentioned

  • XOLREMDI (mavorixafor)

Snippet

Status: Authorised. Therapeutic area: Primary Immunodeficiency Diseases. MAH: Norgine B.V.. Decision date: 19/08/2026. Orphan medicine