Tiziana Life Sciences, Ltd. (NASDAQ:TLSA) ("Tiziana" or the "Company"), a biotechnology company developing breakthrough immunomodulation therapies with its lead development candidate, intranasal foralumab, a fully human, anti-CD3 monoclonal antibody, today announced that a poster, titled "Phase 2a Trial of Intranasal Foralumab – BANYAN, a Healey ALS MyMatch Trial," will be presented by Dr. Pinar Uysal today, Monday, August 24, 2026, from 4:30–6:30 p.m. ET during the Scientific Poster Session in the Nexus Pavilion at the Hyatt Regency Grand Cypress Resort in Orlando, Florida.

Dr. Uysal’s presentation will provide an overview of the BANYAN Trial within the Healey ALS MyMatch program at the Sean M. Healey & AMG Center for ALS at Mass General Brigham. It will cover preclinical data supporting foralumab in ALS, the study design, and the implementation of the ALS MyMatch Common Screening Protocol.

The BANYAN trial is a 3:1 (foralumab: placebo) randomized, placebo-controlled, multicenter Phase 2a study evaluating intranasal foralumab (supported by a grant from the ALS Association and partially funded by the Martha Olson-Fernandez Foundation and the ALS Bridge Foundation) and is designed to assess safety, biomarkers of immune modulation and neuroinflammation (including PET imaging of microglial activation), and early signals of clinical effect in people living with ALS. The trial will be conducted across Network of Excellence for ALS (NEALS) sites and leverages the Healey ALS MyMatch infrastructure for trial conduct. The trial is currently in its operational start up phase, further information regarding enrollment timing and site locations will be provided in a forthcoming press release.