EMA CHMP recommends EU approval of X4 Pharmaceuticals’ mavorixafor for WHIM syndrome

Reuters02-27
EMA CHMP recommends EU approval of X4 Pharmaceuticals’ mavorixafor for WHIM syndrome

X4 Pharmaceuticals said the European Medicines Agency’s Committee for Medicinal Products for Human Use adopted a positive opinion recommending marketing authorization under exceptional circumstances for mavorixafor to treat WHIM syndrome in the European Union. The opinion will be reviewed by the European Commission, with a final decision expected in the second quarter of 2026.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. X4 Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202602270700PRIMZONEFULLFEED9662604) on February 27, 2026, and is solely responsible for the information contained therein.

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