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Tiziana Life Sciences Announces Positive Six-Month Clinical Results in Multiple Sclerosis Patients Treated with Intranasal Foralumab Numeric improvements were seen across key multiple sclerosis measures, including the Mo

Key Takeaway: Tiziana Life Sciences announced positive six-month clinical results for intranasal foralumab in patients with non-active Secondary Progressive Multiple Sclerosis (na-SPMS). The findings show notable improvements in key clinical measures including the Modified Fatigue Impact Scale scores and physical function, indicating potential benefits for this underserved patient population. The safety profile remains favorable and a Phase 2 trial is set to begin screening in November 2023.

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POSITIVE FACTORS

  • Significant improvement in Modified Fatigue Impact Scale scores in treated patients.
  • Efficacy signal observed in a difficult-to-treat population of na-SPMS patients.
  • Intranasal foralumab exhibits an encouraging safety profile and clinical response.

Full Press Release Details

Sciences Announces Positive Six-Month Clinical Results in Multiple Sclerosis Patients Treated with Intranasal Foralumab
NEW YORK, October 16, 2023 -- Tiziana Life Sciences Ltd. (Nasdaq:
TLSA) ("Tiziana" or the "Company"), a biotechnology company developing breakthrough immunomodulation therapies
via novel routes of drug delivery, today announced six-month data showing positive clinical improvements related to Modified Fatigue Impact
Scale (MFIS) scores and similar important clinical measures of physical function in foralumab-treated, non-active Secondary Progressive
Multiple Sclerosis (na-SPMS) patients participating in an Expanded Access (EA) Program. This follows on from previously announced positive
six-month PET scan data which was presented at ECTRIMS 2023.
The findings, which are summarized in table 1 below, show broad based
six month improvements across various key measures for multiple sclerosis. Secondary progressive multiple sclerosis is hallmarked by an
increase of disability over time. The table below shows a stabilization or an improvement in physical function of the various clinical
measures over a six-month period.
Fatigue, as measured above in MFIS, refers to an overwhelming sense
of physical, mental, and emotional exhaustion that is disproportionate to the level of activity or effort exerted. It is a major, common,
and often debilitating symptom experienced by many individuals with MS. It differs from the typical tiredness that everyone experiences
from time to time. In the context of MS, it is called primary fatigue' and is a direct result of damage to the central nervous
system. This kind of fatigue can significantly impact a person's daily life and functioning.
"I am pleased to see the continued clinical response to intranasal
foralumab from patients enrolled in our expanded access na-SPMS program," stated Dr. Tanuja Chitnis, M.D., Principal Investigator
and Professor of Neurology at Harvard Medical School (HMS) and senior neurologist at Brigham and Women's Hospital, a founding member
of Mass General Brigham Healthcare System. "Notably, in this latest clinical update for patients EA 3 through EA 6, we have seen
improvement in the Modified Fatigue Impact Scale scores in three out of four patients, which is significant since fatigue is a major complaint
in this population. We have also seen various degrees of improvement in the Expanded Disability Status Scale, Timed 25-Foot Walk Test,
pyramidal function scores and NeuroQoL Fatigue scores in a disease state that typically shows a decline in function over time.
Howard L. Weiner, M.D., Chairman of Tiziana's
Scientific Advisory Board and Co-Director of the Ann Romney Center for Neurologic Diseases at Brigham and Women's Hospital noted,
"With six patients now dosed in our na-SPMS Expanded Access Program and followed over a six-month period, we are seeing a highly
encouraging efficacy signal in this difficult-to-treat patient population."
Gabriele Cerrone, Chairman, acting CEO and founder of Tiziana Life
Sciences noted "Intranasal foralumab is continuing to show clinical improvements over time in patients with na-SPMS where foralumab
targets inflammation in the brain. Based on the totality of the clinical results seen to-date, I am hopeful that intranasal foralumab
and its anti-inflammatory mechanism of action could provide relief to na-SPMS patients that currently have no available therapies."
Activated T cells play an important role
in the inflammatory process. Foralumab, the only fully human anti-CD3 monoclonal antibody (mAb), 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
demonstrated in patients with COVID and with multiple sclerosis, as well as in healthy normal subjects. The non-active SPMS intranasal
foralumab Phase 2 trial is expected to start screening 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, 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 further inquiries:
Tiziana Life Sciences Ltd
Paul Spencer, Business Development and Investor
+44 (0) 207 495 2379
LifeSci Advisors, LLC

Frequently Asked Questions

What are the recent results for foralumab in MS patients?

Tiziana announced positive six-month clinical results in na-SPMS patients, showing improvements in fatigue and physical function.

How does foralumab affect fatigue in MS patients?

Foralumab has demonstrated significant reductions in fatigue symptoms, improving Modified Fatigue Impact Scale scores in 75% of patients.

What is the mechanism of action of foralumab?

Foralumab modulates T cell function to reduce inflammation by binding to the T cell receptor.

When is the Phase 2 trial for foralumab scheduled to start?

The Phase 2 trial for non-active SPMS is expected to begin screening in November 2023.

What types of clinical improvements were observed?

Improvements were noted in fatigue, disability status, walking tests, and general physical function metrics.

Last updated: Oct 11, 2023