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Tiziana Life Sciences Announces Groundbreaking Study Published in Nature Neuroscience Demonstrating Positive Results for Nasal Anti- CD3 Therapy in Traumatic Brain Injury Traumatic brain injury is a leading cause of deat

Key Takeaway: Tiziana Life Sciences announced the publication of a significant study in Nature Neuroscience, demonstrating that their nasal anti-CD3 monoclonal antibody, foralumab, effectively reduces neuroinflammation and enhances recovery in traumatic brain injury (TBI) models. The study showed correlation between the modulation of the neuroinflammatory response and improved neurological outcomes, including reduced anxiety and cognitive decline. This advancement highlights the potential of foralumab as a groundbreaking treatment for TBI, a condition lacking effective treatments currently. The study's findings also pave the way for further exploration of immune modulation in treating neuroinflammatory diseases.

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POSITIVE FACTORS

  • Publication of a landmark study in Nature Neuroscience indicates strong potential for nasal anti-CD3 therapy.
  • Significant reduction in neuroinflammation and improvement in neurological outcomes such as anxiety and motor skills.
  • The therapy could address a major unmet medical need in traumatic brain injury treatment.

Full Press Release Details

Tiziana Life Sciences Announces Groundbreaking
Nature Neuroscience Demonstrating Positive Results for Nasal Anti-
CD3 Therapy in Traumatic Brain Injury
NEW YORK, February 27, 2025 - 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 the
publication of a landmark study in Nature Neuroscience demonstrating that nasal administration of Tiziana's anti-CD3 monoclonal
antibody significantly reduced neuroinflammation and improved recovery. Modulating the neuroinflammatory response correlated with improved
neurological outcomes. These included, less anxiety, less cognitive decline, and improved motor skills, in a preclinical model of traumatic
The study was led by Saef Izzy, MD, FNCS, FAAN,
a neurologist and head of the Immunology of Brain Injury Program at Brigham and Women's Hospital (BWH), a founding member of the
Mass General Brigham healthcare system. The publication revealed that nasal anti-CD3 therapy induces IL-10 producing regulatory T cells
(Tregs) that migrate to the brain and modulate microglia activity. These Tregs were found to play a pivotal role in reducing chronic microglial
inflammation and enhancing their phagocytic function, ultimately mitigating CNS damage and behavioral deficits associated with TBI.
"This study highlights the critical role
of immune modulation in improving recovery time and outcomes after traumatic brain injury," said Dr. Saef Izzy, lead author and
neurologist at Brigham and Women's Hospital. "We found that nasal anti-CD3 therapy effectively harnesses the body's
own immune system to counteract the damaging effects of neuroinflammation while enhancing the brain's reparative mechanisms. These
findings offer exciting potential for developing a much-needed therapeutic approach for TBI patients."
TBI remains a major unmet medical need, with no
effective treatments currently available to reduce CNS injury and promote recovery. The study demonstrated that blocking the IL-10 receptor
abrogated the benefits of nasal anti-CD3, confirming the pivotal role of IL-10 in the therapeutic effect. Moreover, the adoptive transfer
of IL-10 producing Tregs restored the benefits, further validating the mechanism of action.
positive results from this study provide strong support for advancing nasal anti-CD3 (foralumab) as a novel and promising treatment for
traumatic brain injury," said Dr. Howard L. Weiner, Co-Director of the Ann Romney Center for Neurologic Diseases at BWH. "By
modulating the immune system through simple nasal delivery, we are tapping into a unique and innovative way to treat neuroinflammation
and improve outcomes for TBI patients, which could be in a hospital, at
the road side after an accident or on the playing field in contact sports."
"The Company's proprietary nasal anti-CD3
monoclonal antibody platform has already demonstrated potential in multiple neuroinflammatory and autoimmune diseases. These results further
validate the mechanism of action of foralumab and Tiziana's commitment to further develop transformative therapies for neuroinflammatory
conditions such as Multiple Sclerosis, Alzheimer's disease and ALS," said Ivor Elrifi, CEO of Tiziana Life Sciences. "We
believe nasal foralumab has the potential to be a game-changer in the treatment of traumatic brain injury and other acute brain injuries,
addressing a critical unmet need in medicine."
Publication title: "Nasal anti-CD3
monoclonal antibody ameliorates traumatic brain injury, enhances microglial phagocytosis and reduces neuroinflammation via IL-10-dependent
Treg-microglia crosstalk" Izzy, S., et al. Nature Neuroscience. DOI: 10.1038/s41593-025-01877-7
Foralumab, a fully human anti-CD3 monoclonal antibody,
is a biological drug candidate that has been shown to stimulate T regulatory cells when dosed intranasally. At present, 10 patients with
Non-Active Secondary Progressive Multiple Sclerosis (na-SPMS) have been dosed in an open-label intermediate sized Expanded Access (EA)
Program (NCT06802328) with either an improvement or stability of disease seen within 6 months in all patients. The FDA has recently allowed
an additional 20 patients to be enrolled in this EA program. In addition, intranasal foralumab is currently being studied in a Phase 2a,
randomized, double-blind, placebo-controlled, multicenter, dose-ranging trial in patients with non-active secondary progressive multiple
sclerosis (NCT06292923).
Activated T cells play an important role in the
inflammatory process. Foralumab, the only fully human anti-CD3 monoclonal antibody (mAb) currently in clinical development, binds to the
T cell receptor and dampens inflammation by modulating T cell function, thereby suppressing effector features in multiple immune cell
subsets. This effect has been observed in patients with COVID and with multiple sclerosis, as well as in healthy normal subjects. The
non-active SPMS intranasal foralumab Phase 2 trial (NCT06292923) began screening patients in November of 2023. Immunomodulation by nasal
anti-CD3 mAb represents a novel avenue for treatment of neuroinflammatory and neurodegenerative human diseases.1,2
About Tiziana Life Sciences
Tiziana Life Sciences is a clinical-stage biopharmaceutical
company developing breakthrough therapies using transformational drug delivery technologies to enable alternative routes of immunotherapy.
Tiziana's innovative nasal approach has the potential to provide an improvement in efficacy as well as safety and tolerability compared
to intravenous (IV) delivery. Tiziana's lead candidate, intranasal foralumab, which is the only fully human anti-CD3 mAb currently
in clinical development, has demonstrated a favorable safety profile and clinical response in patients in studies to date. Tiziana's
technology for alternative routes of immunotherapy has been patented with several applications pending and is expected to allow for broad
pipeline applications.
For more information about Tiziana Life Sciences
and its innovative pipeline of therapies, please visit www.tizianalifesciences.com.
Forward-Looking Statements
Certain statements made in this announcement are
forward-looking statements. These forward-looking statements are not historical facts but rather are based on the Company's current
expectations, estimates, and projections about its industry, its beliefs, and assumptions. Words such as anticipates,' expects,'
intends,' plans,' believes,' seeks,' estimates,' and similar expressions
are intended to identify forward-looking statements. These statements are not guarantees of future performance and are subject to known
and unknown risks, uncertainties, and other factors, some of which are beyond the Company's control, are difficult to predict, and
could cause actual results to differ materially from those expressed or forecasted in the forward-looking statements. The Company cautions
security holders and prospective security holders not to place undue reliance on these forward-looking statements, which reflect the view
of the Company only as of the date of this announcement. Actual results may differ materially from
those indicated by such forward-looking statements as a result of various important factors, including: the uncertainties related to market
conditions and other factors described more fully in the section entitled Risk Factors' in Tiziana's Annual Report
on Form 20-F for the year ended December 31, 2023, and other periodic reports filed with the Securities and Exchange Commission.The
forward-looking statements made in this announcement relate only to events as of the date on which the statements are made. The Company
will not undertake any obligation to release publicly any revisions or updates to these forward-looking statements to reflect events,
circumstances, or unanticipated events occurring after the date of this announcement except as required by law or by any appropriate regulatory
For further inquiries:
Tiziana Life Sciences Ltd
Paul Spencer, Business Development, and Investor
+44 (0) 207 495 2379

Frequently Asked Questions

What is Tiziana's lead therapy for traumatic brain injury?

Tiziana's lead therapy is intranasal foralumab, an anti-CD3 monoclonal antibody.

How does nasal anti-CD3 therapy affect neuroinflammation?

Nasal anti-CD3 therapy significantly reduces neuroinflammation and improves recovery.

Who led the study published in Nature Neuroscience?

The study was led by Dr. Saef Izzy from Brigham and Women's Hospital.

What role do Tregs play in TBI treatment?

Tregs produce IL-10, which helps reduce inflammation and mitigates CNS damage.

What does the study imply for TBI treatments?

The study supports advancing nasal anti-CD3 as a novel treatment for TBI.

Last updated: Feb 27, 2025