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Tiziana Life Sciences Announces Six-Month Qualitative Improvement in Neuroimaging in 80% of Multiple Sclerosis Patients Receiving Intranasal Foralumab Qualitative improvements in PET imaging seen in 80% of non-active Sec

Key Takeaway: Tiziana Life Sciences announced significant findings in their Expanded Access Program for intranasal foralumab, reporting that 80% of enrolled non-active Secondary Progressive Multiple Sclerosis patients exhibited qualitative improvements in neuroimaging over six months. This data emerged from qualitative assessments of PET imaging that showed a reduction in microglial activity in the majority of subjects. The company aims to advance its intranasal foralumab program further, supported by ongoing studies and an application for Orphan Drug Designation. Tiziana highlights the potential of their novel drug delivery technology in treating neurodegenerative diseases.

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POSITIVE FACTORS

  • 80% of patients showed a qualitative improvement in neuroimaging.
  • The treatment is positioned as a novel approach for neuroinflammatory diseases.
  • The drug has a favorable safety profile and clinical response in previous studies.
  • Plans for further studies and expansion of the patient cohort indicate potential for continued progress.

Full Press Release Details

Tiziana Life Sciences Announces Six-Month Qualitative
Improvement in Neuroimaging in 80% of Multiple Sclerosis Patients Receiving Intranasal Foralumab
NEW YORK, June 6, 2024 - 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 the qualitative results for all 10 non-active Secondary Progressive Multiple Sclerosis
(na-SPMS) patients enrolled in the intermediate-size patient population Expanded Access (EA) Program receiving foralumab for at least
Tarun Singhal, M.B.B.S., M.D., Director of the PET Imaging Program
in Neurologic Diseases, associate neurologist and nuclear medicine physician at Brigham and Women's Hospital, a founding member
of Mass General Brigham Healthcare System, and Associate Professor of Neurology at Harvard Medical School, commented, "Based on
currently available data from the latest cohort of four Expanded Access patients, three out of the four subjects had findings that suggest
a qualitative reduction in the microglial PET signal over a period of six months of treatment with nasal foralumab. When combined with
my assessment of the first six Expanded Access patients at six months, eight of the ten suggest a qualitative reduction in microglial
PET signal. Further studies are needed to confirm these findings using additional cases and quantitative approaches."
Gabriele Cerrone, Chairman, acting CEO, and founder of Tiziana Life
Sciences, added, "I am thrilled that 80% of the na-SPMS patients who received intranasal foralumab treatment for at least 6-months
have a qualitative reduction of microglial activity as confirmed in these latest PET images. I am also greatly appreciative of Dr. Singhal's
research and look forward to the additional quantitative analysis of the data. With the allowance of an additional 20 patients in the
EA program, the application for Orphan Drug Designation for na-SPMS, and the ongoing Phase 2a trial, Tiziana is rapidly progressing its
intranasal foralumab program in multiple sclerosis."
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
(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, 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 Relations
+44 (0) 207 495 2379
LifeSci Advisors, LLC

Frequently Asked Questions

What percentage of MS patients showed improvement with foralumab?

80% of na-SPMS patients exhibited a qualitative reduction in microglial activity.

What is foralumab used to treat in multiple sclerosis patients?

Foralumab is designed to modulate T cell function and reduce inflammation in MS.

How long were MS patients treated with foralumab in the study?

Patients received intranasal foralumab treatment for a duration of at least six months.

What is Tiziana Life Sciences focusing on with foralumab?

Tiziana is advancing its intranasal foralumab program for treating neuroinflammatory diseases.

What unique approach does foralumab utilize in treatment?

Foralumab uses a novel nasal delivery method to enhance immunotherapy efficacy and safety.

Last updated: Jun 6, 2024