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Teva Says Anti-IL-15 Drug Meets Primary Endpoint in Phase 2a Celiac Disease Trial

By Public Technologies
  • Teva will present pipeline updates at its first R&D Day today, targeting $6–7 billion in innovative medicines revenue by 2030.
  • An anti-IL-15 Phase 2a trial in celiac disease met its primary endpoint; a Phase 2b study is expected in second-half 2027.
  • TEV-'408 is advancing into a Phase 2/3 vitiligo study following encouraging Phase 1b results.
  • Anti-PD-1/IL-2 ATTENUKINE has shown early efficacy signals with a favorable safety profile in an ongoing Phase 1 advanced cancer trial.
  • The pipeline could support one innovative medicine launch annually through 2030, with more than $10 billion in combined peak sales potential.


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. Teva Pharmaceutical Industries Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202611110730OMX_____CNEWS_EN_GNW1001302977_en) on November 11, 2026, and is solely responsible for the information contained therein.

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