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Zura Bio's Tibulizumab Misses Primary Endpoint in Phase 2 Hidradenitis Suppurativa Trial

By Public Technologies
  • Zura Bio is discontinuing tibulizumab development in hidradenitis suppurativa following newly announced Phase 2 TibuSHIELD results.
  • The trial missed its primary efficacy endpoint at both doses; key secondary endpoints were also not met.
  • Tibulizumab development continues in systemic sclerosis, with TibuSURE topline results expected in the first half of 2027.
  • The planned NEXUS-PMR study in polymyalgia rheumatica is expected to report data in the fourth quarter of 2028.
  • Cash and cash equivalents totaled $187.7 million as of September 30, 2026, supporting planned operations through at least year-end 2028.


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. Zura Bio Ltd. published the original content used to generate this news brief via Business Wire (Ref. ID: 20261109871255) on November 09, 2026, and is solely responsible for the information contained therein.

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