XBiotech vilamakitug Phase II axial spondyloarthritis IND clears FDA review without hold

XBiotech, Inc.

XBiotech, Inc.

XBIT

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  • XBiotech’s IND for its V-SPINE Phase II trial of vilamakitug in active axial spondyloarthritis cleared the FDA’s 30-day review without a clinical hold.
  • The decision authorizes U.S. patient enrollment, restarting the company’s rheumatology program.


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. XBiotech Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202606150900OMX_____CNEWS_EN_GNW9746284_en) on June 15, 2026, and is solely responsible for the information contained therein.

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