Annexon Files Marketing Authorization Application for Tanruprubart in Europe

Reuters

01/12

Annexon Inc. announced that it has filed a Marketing Authorization Application $(MAA)$ in Europe for tanruprubart, a targeted fast-acting therapy for Guillain-Barré Syndrome (GBS). The company also plans to submit a Biologics License Application (BLA) in the United States using data from U.S. and European trials in 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. Annexon Inc. published the original content used to generate this news brief on January 12, 2026, and is solely responsible for the information contained therein.

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