Tiziana Life Sciences Ltd. has announced the dosing of the first patient in its Phase 2 randomized, placebo-controlled clinical trial evaluating intranasal foralumab in patients with early Alzheimer's disease. The study will assess foralumab, a fully human anti-CD3 monoclonal antibody, as both a monotherapy and in combination with FDA-approved anti-amyloid therapies, lecanemab and donanemab. The trial is based on evidence of persistent neuroinflammation in Alzheimer's patients treated with anti-amyloid therapies. Results from the trial have not yet been presented and will be generated in the future.
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. Tiziana Life Sciences Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9603623) on December 17, 2025, and is solely responsible for the information contained therein.
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